PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of cancersMDPI Open Access Journalshomethis articlethis journalinstructions for authorssubscribecancers
 
Cancers (Basel). 2010 September; 2(3): 1661–1682.
Published online 2010 September 9. doi:  10.3390/cancers2031661
PMCID: PMC3837330

Interaction of Stellate Cells with Pancreatic Carcinoma Cells

Abstract

Pancreatic cancer is characterized by its late detection, aggressive growth, intense infiltration into adjacent tissue, early metastasis, resistance to chemo- and radiotherapy and a strong “desmoplastic reaction”. The dense stroma surrounding carcinoma cells is composed of fibroblasts, activated stellate cells (myofibroblast-like cells), various inflammatory cells, proliferating vascular structures, collagens and fibronectin. In particular the cellular components of the stroma produce the tumor microenvironment, which plays a critical role in tumor growth, invasion, spreading, metastasis, angiogenesis, inhibition of anoikis, and chemoresistance. Fibroblasts, myofibroblasts and activated stellate cells produce the extracellular matrix components and are thought to interact actively with tumor cells, thereby promoting cancer progression. In this review, we discuss our current understanding of the role of pancreatic stellate cells (PSC) in the desmoplastic response of pancreas cancer and the effects of PSC on tumor progression, metastasis and drug resistance. Finally we present some novel ideas for tumor therapy by interfering with the cancer cell-host interaction.

Keywords: pancreas carcinoma, pancreatic stellate cell, tumor desmoplasia, EMMPRIN, chemoresistance

1. Introduction

In the United States of America, Europe and Japan, the incidence of pancreatic cancer has risen slowly during the last few decades. Pancreatic ductal adenocarcinoma (PDA) is now the fourth leading cause of cancer related death among both men and women in the U.S. [1]. Because this cancer shows no symptoms in its early stage and has therefore a low probability of diagnosis, approximately 80–90% of the patients present with local infiltration or metastatic disease at the time of initial diagnosis [2]. Therefore only 15–20% of the patients are candidates for surgical resection, which is the only chance for cure. The median survival time of patients with metastatic pancreas cancer is <6 months and the overall five-year survival rate is less than 5%.

More than 90% of the pancreas cancers represent PDA, which are characterized by a late detection, an aggressive growth, local invasion into adjacent tissue, a rapid progression, early systemic dissemination [3], late diagnosis and a relative resistance to conventional chemo- and radiotherapy [4,5]. After surgical resection local recurrence occurs in the majority of patients. In addition, a strong “desmoplastic reaction” is characteristic for PDA [6,7]. Fibroblasts, myofibroblasts and activated stellate cells produce the different connective tissue components such as collagens, fibronectin and proteoglycans [8]. As shown by Immamura et al. [8] in pancreas cancer and tumor associated chronic pancreatitis, the collagen content is 3-fold higher compared to normal pancreas. In addition, the proportion of the collagen types I, III and V is comparable to ethanol induced chronic pancreatitis, tumor associated chronic pancreatitis and pancreas cancer [8]. Whereas in pancreas cancer, collagen synthesis is associated with spindle shaped cells (fibroblasts and myofibroblasts), matrix-metalloproteinases (MMPs) and tissue-inhibitors of MMPs (TIMPs) are produced by both, stromal and tumor cells [9].

In his “Frank Brooks Memorial State of the Art Lecture in basic Sciences” at the 2001 Annual APA-meeting, M.G. Bachem presented data for the first time indicating an interaction of PSC with tumor cells. One year later, Yen et al. [10] described a pronounced increase in the number of α-smooth muscle actin positive cells in PDA and suggested that these cells might represent activated PSC producing the connective tissue surrounding carcinoma cells. Thereafter several research groups studied the role of PSC in pancreas cancer [11,12,13,14].

2. Pancreatic Stellate Cells

In an earlier report, fibroblast-like cells were suggested to be responsible for the collagen synthesis resulting in pancreas fibrosis [15]. However, as shown later, the matrix producing cells in pancreas express α-smooth muscle actin (αSMA) and show similarities to activated hepatic stellate cells (HSC) or myofibroblast-like cells [16,17]; for a review see [18]. Normal fibroblasts do not express desmin or αSMA. In addition, by using microarray technology to analyze the gene expression profile of (i) normal fibroblasts; (ii) activated HSC and (iii) activated PSC, respectively, significant differences between stellate cells (HSC and PSC) and fibroblasts could be demonstrated [19]. Vitamin A storing cells have been found in different organs of vertebrates such as the liver, pancreas, kidney, lung, skin and others. HSC have long been known to play a major role in repair after injury and in liver fibrogenesis [20,21]. The cellular vitamin A content, primarily retinyl palmitate, is visible during excitation with UV-light as a rapidly fading fluorescence. Some cytoskeleton proteins might also be used to identify these cells (see Figure 1). PSC are of mesangial origin but, as we have learned recently in injury and cancer, part of these cells also originate from bone marrow (see below).

Figure 1
Characteristics of quiescent (fat-storing phenotype) and activated PSC (myofibroblast-like phenotype). In acute and chronic pancreatitis, but also in pancreas carcinomas, PSC change their phenotype from a quiescent fat-storing phenotype to a highly active ...

Vitamin A storing cells in the pancreas were first described in the year 1982 by Watari et al. using electron and fluorescence microscopy of mice pancreas tissue after vitamin A loading [22]. A few years later, vitamin A storing cells were found in normal human and rat pancreas and in fibrotic human pancreas [23]. In 1998 we, and the Apte-Wilson-Group in Sydney, isolated and characterized vitamin A storing stellate-shaped cells from rat and human pancreas [16,17]. Because of their similarity to HSC we named the cells pancreatic stellate cells [17]. In normal pancreas low numbers of quiescent fat-storing PSCs can be detected interlobular and in the periacinar space [16,17]. Comparable to the stellate cell-activating mechanisms in liver injury, also in acute and chronic pancreatitis and in pancreas cancer (but also in primary culture), the cells are activated and change their phenotype (Figure 1). The fat storing phenotype of PSC is quiescent (low mitotic index, low capacity to produce matrix and growth factos), has numerous perinuclear fat droplets containing retinyl-palmitate and expresses the cytofilaments vimentin, desmin, glial fibrillary acidic protein (GFAP), Nestin and synemin (Figure 1).

In pancreas injury (e.g., acute and chronic pancreatitis), but also in pancreas carcinoma [24], the quiescent fat-storing phenotype of PSC loses its retinoids, develops a prominent rough endoplasmic reticulum and transforms into a highly active matrix producing myofibroblast-like cell (Figure 1). This cell type is primarily found in interlobular fibrotic areas or adjacent to carcinoma cells. The activated PSC (myofibroblast-like) are vimentin and αSMA positive, have a high mitotic index, express the receptors for PDGF and TGFß, express ICAM-I, are able to contract and move, produce the extracellular matrix components collagen I, III, XI, fibronectin and periostin, also synthesise MMPs and TIMPs and release the growth factors PDGF, FGF, TGFß1, CTGF, IL1ß, IL-6, IL-8, IL-15, Rantes, MCP1, ET1 and VEGF (see Figure 1). In addition, PSC which have been isolated from pancreas carcinomas also contain lipid droplets [14] and express vimentin and αSMA (Figure 2). These tumor derived PSCs also produce collagen I and III, fibronectin, growth factors, and proteases in significant amounts [13,14,24].

Figure 2
Immunofluorescence microscopy of cultured PSC, which have been isolated from pancreatic ductal adenocarcinoma. (a) vimentin immunofluorescence (red); (b) alpha-smooth muscle actin immunofluorescence (red). Cell nuclei are stained blue (Hoechst ...

Cell culture experiments have shown that TGFß, TNFα, IL-1, IL-6, IL-8, ethanol, acetaldehyde, and oxidative stress stimulate the transformation from the fat storing phenotype to the myofibroblast-like phenotype (Figure 1). Activated PSC are stimulated by injured acinar cells [25], aggregating platelets, inflammarory cells, ethanol and acetaldehyde to proliferate, produce matrix, and MMPs [26], and synthesize growth factors and cytokines (Figure 3) ([27]). The most important paracrine factors stimulating fibrogenesis in activated PSC are TGFß1, FGF, PDGF, ET-1, and acetaldehyde. TNFα, IL-1, TGFß, and IL-6 are related to ECM degradation and remodeling (Figure 3). Because activated PSC synthesize TGFß1, CTGF, PDGF, ET-1, IL1, IL6, IL8, activin-A, periostin, and COX-2, autocrine stimulatory loops might also play a role in chronic pancreatitis and PDA (Figure 3). Additionally, activated PSC also produce IL15, which reduces lymphocyte apoptosis, again leading to further PSC activation [28].

Figure 3
Paracrine and autocrine stimulation of activated pancreatic stellate cells in culture. Injured acinar cells, activated inflammatory cells, aggregating platelets, ethanol and acetaldehyde stimulate PSC proliferation, matrix- and MMP-synthesis and PSC motility. ...

Accumulating evidence suggests that part of the PSC in fibrotic pancreas are derived from bone marrow [29,30], express several stem/progenitor cell markers such as CD34, Nestin, p75NTR, GFAP, Bcrp1, Aldh, Notch (for review see [31]), and are able to differentiate into other pancreatic cell types [32]. Pan and coworkers have shown that bone marrow-derived progenitor cells contribute to the stellate cell and inflammatory cell population near metaplastic tubular complexes and carcinoma cells [33]. Based on their data, these authors suggest that bone marrow-derived progenitor cells could influence pancreatic cancer growth by modulating tumor microenvironment [33].

3. Cell-Cell Interactions between PSC and Carcinoma Cells

Experimental and clinical data indicate that acute and chronic pancreatitis represent potent risk factors for PDA [34,35,36]. Tissue injury (e.g., acute pancreatitis) [37], oncogene activation like Hedgehog/Ras [38,39,40] or Notch [41,42] and TGFα activation [43] induce and accelerate acinar-ductal metaplasia and PanIN development. Notch activity is thought to play a major role in cancer development because TGFα induced acinar-to-duct conversion requires Notch activation [42], and Notch and Kras coactivation cause a rapid acinar-to-duct-like phenotype [41]. Chronic pancreatitis also accelerates Kras-driven PanIN and PDA development [34]. In addition, accumulating evidence indicates that in tissue injury, and pancreatitis activation of PSC, is linked to tumor progression. Erkan and colleagues quantified the extent of activated stromal cells in situ by quantifying what they called the “activated stroma index” (ASI) [44]. They stained consecutive tissue sections of cancer patients with antibodies against aSMA or with aniline blue revealing collagen deposition. What they observed was that a high coefficient of aSMA / collagen staining correlated with a poor prognosis and vice versa. This indicates that high PSC numbers and a high activation grade of PSC (strong aSMA staining), but not a strong desmoplastic reaction (collagen synthesis), are related to tumor progression.

The cell type that gives rise to precursor lesions, termed pancreatic intraepithelial neoplasia (PanIN), is still in debate. Pancreatic duct epithelial cells [45] or centroacinar cells [46,47] have been suggested as cancer-initiating cells, but evidence accumulates that acinar cells represent the bad guys [41,48,49,50]. There are also hints that PSC might participate in the initiation of PDA [51]. Beside the growth factors mentioned above, other factors might also be involved in CC-PSC interaction and contribute to cancer progression (see Figure 4). Firstly, PSC store retinaldehyde esters within lipid droplets, which may be oxidized by aldehyde dehydrogenases to retinoic acid (RA). Upon activation of PSC, the lipid droplets disappear, thereby releasing their contents. RA promotes cell differentiaton—a physiological process needed to maintain tissue homeostasis, e.g., for restricting acinar cell proliferation. Following continuous activation of PSC though, RA stores may be depleted and proliferation of acinar cells may continue once initiated. Secondly, collagen I, which is produced by activated PSC, has been shown to directly weaken E-cadherin mediated cell-cell interactions of tumor cells, and to stimulate cell proliferation by b-catenin-mediated up-regulation of c-myc and cyclin D1 expression [52]. Additionally, collagen I was shown to increase N-cadherin expression and the metastatic potential of CC in vivo [53]. In this context, one might speculate that, for example, phagocytosis of necrotic acinar cells [54] or bacteria [55] by PSC may lead to local activation of PSC and collagen production, finally stimulating acinar cell proliferation. In adult mice chronic pancreatitis has been shown to be essential for the induction of ductal adenocarcinomas by K-Ras oncogenes [34], and from humans it is known that both idiopathic and alcoholic pancreatitis are associated with a 15-fold higher risk of developing pancreatic cancer [56]. In summary, the local activation of PSC, simply as a result of local tissue injury, may in turn ‘accidentally’ initiate or promote cell proliferation of acinar cells.

Figure 4
Interaction of PSC with pancreas carcinoma cells. Pancreas carcinoma cells (CC) accelerate transformation of quiescent PSC to the myofibroblast-like phenotype. This cell type is attracted by CC and stimulated to proliferate, produce ECM and growth factors. ...

Furthermore, in recent years we have learned from different tumors that the tumor microenvironment plays an active role in tumor progression, invasion, chemoresistance, escape from apoptosis and anoikis and metastasis [57,58,59,60]. At the invasion front, stroma and tumor cells interact and exchange factors (enzymes, growth factors, cytokines) that degrade local ECM and stimulate migration, promote proliferation, angiogenesis and tumor cell survival. Pancreas carcinoma microenvironment contains the angiogenesis stimulating factors VEGF, PDGF, FGF1, FGF2, collagen-I, periostin, adrenomedullin, prokineticin-1, MMPs and uPA, the migration-stimulating factors PDGF, EGF and SDF-1, proliferation stimulating factors such as TGFß, FGF2, PDGF, EGF, CTGF, adrenomedullin [61], Gal-3, and SDF-1, invasion promoting factors such as MMPs, thrombospondin [62], uPA, and tPA, and factors responsible for drug resistance (NO, IL-1ß) and inhibition of anoikis/apoptosis (collagens, fibronectin, laminin). Tumor cells, as well as fibroblasts, myofibroblasts, and in particular activated PSC, are responsible for the production of these factors (see Figure 4).

To study PSC-CC interactions, we performed co-culture experiments of CC and PSC (see Figure 5) or stimulated cultured PSC with CC-supernatants and vice versa. The results and the data of others regarding the interaction of PSC with carcinoma cells are summarized in Figure 4. By producing TGFß1 and other fibrogenic mediators, pancreas CC stimulate the transformation of the quiescent fat-storing phenotype of PSC to the highly active myofibroblast-like phenotype. In addition, CC attract PSC (Figure 5c,d) and stimulate motility, proliferation and matrix synthesis of PSC [14,27]. The result of this stimulation is a strong desmoplastic reaction surrounding carcinoma tissue [13,14]. The activated PSC proliferate strongly in response to PDGF, IGF1, and ET-1. Migration of PSC is stimulated by PDGF, matrix synthesis is stimulated primarily by TGFβ1, FGF-2, and sonic hedgehog. In addition, CC induce MMP synthesis via the release of IL1, TGFß1, TNFα, and EMMPRIN. In particular MMP-2, MMP-9, and plasminogen-activator (uPA) are involved in tumor dissemination. As shown by Gress et al., MT1-MMP, MT2-MMP, MMP-2, MMP-9 are strongly expressed in pancreas cancer [9]. Recent data from our group shows that PSC significantly contribute to MMP-2 secretion in the desmoplasia of pancreatic cancer in vivo and in vitro [63]. MMP-2 staining was found primarily in PSC adjacent to cancer cells [14] and secretion of MMP-2 by PSC by far exceeds that of cancer cells [63], although pancreas carcinoma cells express some MMP-2. Furthermore, there is evidence that cancer cells induce uPA expression in stromal cells, which then bind to the urokinase receptor (uPAR) expressed on cancer cells (for review see [64]). After binding, uPA converts plasminogen to plasmin, which then degrades fibrin, collagen IV, fibronectin and laminin. Beside the action of MMPs, this also enables tumor cells to migrate through tumor surrounding ECM.

Figure 5
Microphotographs of PSC (isolated from PDA) in co-culture with primary pancreas carcinoma cells (ULA-PaCa). (a) phase contrast; (b) alpha-smooth muscle actin immunofluorescence (red); (c) vinculin, red-yellow, f-actin, green; (d) paxillin, red-yellow; ...

In particular, MMPs are suggested to play an important role in cancer progression that is in early metastasis, angiogenesis, and release of growth factors from ECM [65,66]. Early trials with MMP inhibitors though did not result in significant benefits for cancer patients, probably due to their application in late stage cancer, their usage as monotherapy, and missing information about good and bad responders [66]. However, new target-specific inhibitors are being developed [67,68].

Data from our group [14,63] and from the lab of H. Fries [69] have shown that CC express EMMPRIN (Extracellular Matrix Metalloproteinase Inducer) and thereby stimulate the synthesis of MMPs in PSC. EMMPRIN, also named Basigin or CD147, which is a type I transmembrane glycoprotein, has been extensively studied because it is involved in tumor cell migration and invasion [70,71,72,73], apoptosis [74,75], angiogenesis [76,77,78], and chemoresistance [79,80] in a variety of cancers (reviewed by [81]). In pancreatic cancer, serum levels of EMMPRIN are elevated compared to healthy volunteers, though serum levels do not correlate with TNM status [69]. Experiments in nude mice showed that EMMPRIN promotes tumor growth of CC in vivo [82].

Most effects of EMMPRIN have been reported to be mediated by the induction of MMPs. For example, positive correlations between the expression of MMPs and EMMPRIN in various cancers can be found in numerous reports [83,84]. Furthermore, co-culture of cancer cells with stromal fibroblasts induces MMPs, which can be blocked by EMMPRIN antibodies [72,85,86]. In addition, there is a positive feedback regulation of EMMPRIN and MMP-dependent generation of soluble EMMPRIN [87]. Finally, the up-regulation of MMP expression in PSC by CC-derived EMMPRIN accelerates tumor growth in vitro and in vivo [63]. Because of the central role of EMMPRIN in tumor progression, antibody- or siRNA-based therapies have already been tested in mouse models of various cancers with some success [82,88,89]. However, some evidence exists that EMMPRIN does not induce MMP-synthesis in certain cell systems, tumor types, and animal models. In murine melanoma cells, for example, knockdown of EMMPRIN did not reduce the tumor cell-mediated induction of MMP-2, -9, and -14 both in vitro and in vivo [90], but impaired angiogenesis and metastasis formation [77].

EMMPRIN exists as high and low glykosylated isoform. Their proportion is partly regulated by the interaction of EMMPRIN with caveolin-1 in the Golgi complex [91] and varies between different pancreas CC lines [63,69]. In order to mediate intercellular signals, the transmembrane protein EMMPRIN can be solubilized from the cell membrane by microvesicle shedding [92,93] or by proteolysis of the extracellular part of EMMPRIN by MMPs [87,94].

PSC also express varying amounts of EMMPRIN [63,69]. This is of interest, because so far there is no convincing data identifying the receptor for EMMPRIN. The most favored mechanism of action of EMMPRIN is the homophilic interaction of soluble EMMPRIN and membrane-bound EMMPRIN [86,95]. This interaction and the consecutive induction of MMPs can be blocked by unglycosylated recombinant EMMPRIN—the ineffective form of the protein—or by antibodies against EMMPRIN [86]. The main obstacle of this proposed mechanism is the way by which the signal is transduced into the cell. Obviously, EMMPRIN itself has no kinase or phosphatase activity and is not coupled to ion channels or any other known signal transduction molecules. However, following addition of soluble EMMPRIN to cultured cells activation of downstream mediators such as p38-MAPK [96], SAPK/JNK [73], or phospholipase A2 and 5-lipoxygenase [97] have been described.

Another possibility of EMMPRIN signaling might be endocytosis of dimeric or multimeric EMMPRIN (following binding of soluble EMMPRIN) with other components, for example cyclophilin B, which has been shown for the entry of measles virus into epithelial cells [30]. Recently, in vitro and in vivo experiments have revealed the interaction of EMMPRIN with monocarboxylate transporters, proteins, which confer lactate export from cells in tissues with reduced oxygen supply like solid tumors [82], providing an additional explanation for the tumor promoting effect of EMMPRIN in conjunction with the Warburg hypothesis [98].

Another way EMMPRIN can exert its effects is by the direct binding of MMPs to the tumor cell surface and subsequent local organization of the enzymes in the cell membrane (e.g., a directed localization towards invadopodia), which has been shown for lung carcinoma cell-derived MMP-1 [99]. This strongly accumulated MMP could again locally activate further MMPs, for example PSC-derived MMP-2 and MMP-9.

Mutual activation and inactivation of MMPs plays an important role in regulation of MMP activity (for review see [100]). Additionally to EMMPRIN (and other factors), these proteases are also tightly regulated by tissue inhibitors of MMPs (TIMPs). In PDA, an imbalance of MMP and TIMP expression compared to healthy controls has been observed [101]. As tumor cells proliferate, the total amount of MMPs (inactive pro-MMPs as well as active MMPs) would concomitantly increase and further activate PSC-derived MMPs. Hereby, a positive feedforward loop on ECM remodeling is generated.

By producing multiple cytokines and growth factors including PDGF, FGF, TGFβ1, CTGF, IL-1β, IL-6, IL-8, SDF-1, Rantes, TNFα, MCP-1, and ET-1 activated PSC also influence proliferation, motility, invasion, and chemoresistance of CC (see Figure 4). In addition, via the production of VEGF, PDGF, FGF1, FGF2, IL-8, coll-I, periostin, adrenomedullin, prokineticin-1, MMPs, and uPA, activated PSC also promote angiogenesis (see Figure 4). CC proliferation is stimulated via the growth factors TGFß, FGF2, and PDGF [13,14], invasion via the production of MMPs, and motility via PDGF and EGF. These data have been confirmed by C. Logsdon’s group which has shown that PSC supernatants increased tumor cell proliferation, migration, invasion, and colony formation [102]. Furthermore, gemcitabine and radiation therapy were less effective in tumor cells treated with PSC supernatant. Although all the responsible mediators have not been identified as yet, activation of MAPK and Akt pathways have been observed after addition of PSC supernatant to cultured tumor cells [102]. Very recently X. Wang’s group identified another soluble factor in PSC supernatant (stromal cell-derived factor-1 = SDF-1) promoting proliferation, migration and invasion of cancer cells [103]. In addition, very interestingly the presence of PSC increased the incidence of tumor formation when limiting numbers of CC were orthotopically injected into nude mice [102]. These data were confirmed by M. Apte’s group using orthotopically transplanted MiaPaCa-2 cells in combination with PSC from different human donors [104]. They identified PDGF as the primarily responsible factor for the tumor promoting effects of PSC (in vitro). Interestingly, the group also reported the existence of αSMA-positive human cells in liver nodules together with a higher incidence of distant metastases on transplantation of CC with PSC than without (50% vs. 10%), indicating that some PSC might have comigrated with the CC. Our in vivo data, showing the induction of subcutaneous tumors in nude mice, also indicate that, in the presence of PSC, tumor progression is accelerated [13,63]. Others have shown that direct contact of tumor cells with PSC activated the Notch signaling pathway and resulted in even stronger stimulation of tumor cell proliferation compared to stimulation by supernatant [105].

In summary, all these observations support the hypothesis that PSC provide a microenvironment which is advantageous for tumor cell growth and survival. Interestingly, several growth factors, such as TGFß, FGFs, PDGF-BB and insulin-like growth factor-I (IGF-1) are sequestered within the ECM, which thus acts as a sponge for these factors [105]. Proteases from CC or MMPs from PSC (which are induced through EMMPRIN from CC) might degrade the ECM and release these bound growth factors.

As shown in Figure 6, we designed a set of experiments to demonstrate the release of growth factors by degradation of ECM. Activated PSC were cultured in 6-well plates until confluency. Then, the medium was changed and in the absence of fetal calf serum new medium was conditioned for three days. This PSC supernatant was added to cultured pancreas CC (Panc1 and SW850) and proliferation of the CC was quantified by BrdU-incorporation (see Figure 6a and 6b). Cultured PSC were washed and then lysed using distilled water. After a further three washing steps, the remaining ECM was degraded at 37 °C by addition of 2 mL CC supernatant (containing proteases and MMPs). The degraded matrix was then added to cultured CC and proliferation was again measured by BrdU incorporation (Figure 6a and c). In addition, PSC supernatant and degraded PSC-matrix were preincubated for 1 h with neutralizing antibodies against TGFß1, bFGF, and PDGF-AB.

Figure 6
Effect of PSC supernatants (PSC-SN) and degraded extracellular matrix on proliferation (BrdU-incorporation) of cultured Panc1 cells. (a) Activated PSC were cultured in 6-well plates until confluency. Then, medium was changed and in the absence of fetal ...

As shown in Figure 6a and 6b, PSC-conditioned medium (PSC-SN) and degraded PSC matrix both stimulate the proliferation of Panc1 cells by almost 40% compared to control. Preincubation with neutralizing antibodies against TGFß1 and bFGF identified both factors as mitogens for CC. Similar results were obtained using SW850 cells instead of Panc1. In summary, these experiments demonstrate that (i) TGFß1 and bFGF are produced by cultured PSC; (ii) both factors are sequestered in the ECM and might be released by matrix degradation; (iii) both factors stimulate proliferation of pancreas carcinoma cell lines.

4. Role of PSC in Chemoresistance

As mentioned above, surgical resection of PDA in combination with chemo- or radiotherapy is the only chance for cure. However, only 15–20% of the patients are candidates for surgical intervention. Another problem is the development of chemo- and radioresistance in PDA. The synthetic nucleoside analogue gemcitabine, which is the most commonly used drug for chemotherapy of PDA, is a prodrug, which needs to be transported into the tumor cells followed by activation through various enzymes. Recent data show that, among these proteins, a high expression of equilibrative nucleoside transporter 1, which enables the entry of the compound into the cells, correlates with higher survival in gemcitabine-treated patients [107]. Within cells, gemcitabine is phosphorylated by various enzymes and inhibits ribonucleotide reductase and DNA synthesis [108], but phosphatases, like 5’-nucleotidase, or cytidine deaminase, which irreversibly deactivate the drug, again may limit this process. Additionally, as one might expect, there is a positive correlation between the expression of anti-apoptotic genes of the Bcl-2 family, like Bcl-XL, and resistance of CC against gemcitabine or 5-fluorouracil [109]. Up-regulation of these anti-apoptotic genes is mainly conferred by mutations of nuclear factor kB (NF-κB), variations in signaling pathways upstream of NF-κB, or continuous auto- and paracrine stimulation of NF-κB activity by various growth factors and cytokines. Inhibition of NF-κB increased apoptosis and thereby reduced chemoresistance [110].

Participation of PSC in the above mentioned mechanisms has not been investigated so far, but there are several observations indicating that PSC might play a significant role in both the manifestation and progression of chemoresistance. PSC-conditioned medium, for example, directly protects CC against the cytotoxicity of gemcitabine: Only 9% of BxPC3 cells in the presence, compared to 34% of cells in the absence, of PSC-conditioned medium were TUNEL-positive after 48 hours treatment with 100 µM gemcitabine [102].

Among others, CC express IL-1β, which confers constitutive NF-κB activity and chemoresistance via autocrine stimulation [111]. At this point, PSC come into play: IL-1β leads to the expression of inducible nitric oxide synthase (iNOS) in PSC [112]. PSC do not express IL-1β, but, once expressed, the ‘constitutively’ active iNOS—being independent on enzyme regulators like calcium/calmodulin—releases nitric oxide (NO). The freely diffusible molecule NO increases, as a paracrine mediator, the expression of IL-1β in CC, resulting in a positive feedback loop. Co-culture experiments using either PSC or PSC-conditioned medium revealed significantly reduced rates of etoposide-induced apoptosis (>50% reduction) in CC compared to CC mono-cultures. This effect was blocked by either an IL-1β receptor antagonist or the iNOS inhibitor aminoguanidine, but enhanced by the NO donor S-nitroso-N-acetyl-D,L-penicillamine (SNAP). Additionally, histology revealed both the expression of IL-1β and iNOS in human pancreatic adenocarcinoma samples [112]. In this context, hypermethylation of caspase-3, -7, -8, and -9 genes, resulting in reduced expression of these effector enzymes of apoptotic signaling, seems to be responsible for the increased resistance to apoptosis [113].

Another research group has shown that culture of CC on ECM protein-coated dishes (including fibronectin, laminin, collagen type I and IV) directly influences CC proliferation and increases the resistance of CC against the cytotoxicity of 5-fluorouracil, cisplatin, and doxorubicin [114]. This suggests that ECM proteins, abundantly expressed by PSC, might directly promote resistance against anticancer drugs. Interestingly though, none of these ECM proteins changed gemcitabine-mediated cytotoxicity (75–400 nM; 72 hours) in any CC line investigated (Capan-1, Panc-1, MiaPaCa-2) [114], indicating that the increased resistance against anticancer drugs mediated by ECM proteins alone does not adequately reflect the situation in vivo.

Finally, multicellular layer experiments, used as in vitro models for solid tumors, suggest a limited penetration of anticancer drugs through tumor tissues [115]. In case of PDA, a possible candidate gene directly involved in such an increased chemoresistance is the glycoprotein decorin, which is highly expressed on both the mRNA and protein level in activated PSC. It leads to decreased PCC proliferation, but increased gemcitabine resistance, probably due to direct binding of growth factors (affecting proliferation) [116] and small molecules like gemcitabine via it’s leucine-rich domains. The net effect of decorin on proliferation (inhibition) and chemoresistance (increase) in vitro is to slow down CC growth [117].

A recent study reported major progress with respect to reducing chemotherapy resistance in PDA. Inhibition of hedgehog signaling (involved in tumor-stroma interaction as mentioned above) in a murine model of PDA, reduced stromal expansion, thereby increasing intratumoral vascular density and intratumoral concentration of gemcitabine, leading to transient stabilization of disease [118].

In summary, accumulating data indicate that PSC participate in the development of chemoresistance in PDA. Accordingly, research focusing on the improvement of anticancer drug efficiency should not exclusively study CC, but always consider the influence of stromal cells.

5. Conclusions

In recent years, it has been established that cancer growth and spread are strongly influenced by the microenvironment. However, presently the molecular signals involved in the tumor-host cross-talk have only partly been identified. Hopefully in the near future, new therapeutic options might be developed, which directly interfere with the tumor-host cross-talk. The most promising cellular target for anti-stromal treatment could be the matrix and growth factor producing PSCs and endothelial cells playing a central role in angiogenesis. In chronic pancreatitis, cancer initiation and progression might be inhibited, also through inactivation of PSC, causing a reduction of matrix remodeling. Recently, it has been shown that forced expression of peroxisome proliferator-activated receptor g (PPARγ), or CCAAT/enhancer binding protein a (C/EBP-α), induced a phenotypic switch from activated to quiescent PSCs in vitro, which was dependent on the expression of albumin [119]. Effects on MMP expression and net effects on tumor progression in vivo, however, await further experiments.

Acknowledgements

This work was supported by Deutsche Forschungsgemeinschaft (SFB 518, project A7 to M.G.B.).

References

1. Jemal A., Siegel R., Ward E., Hao Y., Xu J., Thun M.J. Cancer statistics, 2009. CA Cancer J. Clin. 2009;59:225–249. doi: 10.3322/caac.20006. [PubMed] [Cross Ref]
2. Cleary S.P., Gryfe R., Guindi M., Greig P., Smith L., Mackenzie R., Strasberg S., Hanna S., Taylor B., Langer B., Gallinger S. Prognostic factors in resected pancreatic adenocarcinoma: Analysis of actual 5-year survivors. J. Am. Coll. Surg. 2004;198:722–731. doi: 10.1016/j.jamcollsurg.2004.01.008. [PubMed] [Cross Ref]
3. DiMagno E.P., Reber H.A., Tempero M.A. AGA technical review on the epidemiology, diagnosis, and treatment of pancreatic ductal adenocarcinoma. American Gastroenterological Association. Gastroenterology. 1999;117:1464–1484. [PubMed]
4. Brand R.E., Tempero M.A. Pancreatic cancer. Curr. Opin. Oncol. 1998;10:362–366. doi: 10.1097/00001622-199807000-00014. [PubMed] [Cross Ref]
5. Warshaw A.L., Fernandez-del Castillo C. Pancreatic carcinoma. N. Engl. J. Med. 1992;326:455–465. doi: 10.1056/NEJM199202133260706. [PubMed] [Cross Ref]
6. Cruickshank A. Pathology of the Pancreas. Springer-Verlag; London, UK: 1986. Solid carcinomas of the exocrine pancreas; pp. 155–177.
7. Pandol S., Edderkaoui M., Gukovsky I., Lugea A., Gukovskaya A. Desmoplasia of pancreatic ductal adenocarcinoma. Clin. Gastroenterol. Hepatol. 2009;7:S44–S47. doi: 10.1016/j.cgh.2009.07.039. [PubMed] [Cross Ref]
8. Imamura T., Iguchi H., Manabe T., Ohshio G., Yoshimura T., Wang Z.H., Suwa H., Ishigami S., Imamura M. Quantitative analysis of collagen and collagen subtypes I, III, and V in human pancreatic cancer, tumor-associated chronic pancreatitis, and alcoholic chronic pancreatitis. Pancreas. 1995;11:357–364. doi: 10.1097/00006676-199511000-00007. [PubMed] [Cross Ref]
9. Gress T.M., Muller-Pillasch F., Lerch M.M., Friess H., Buchler M., Adler G. Expression and in-situ localization of genes coding for extracellular matrix proteins and extracellular matrix degrading proteases in pancreatic cancer. Int. J. Cancer. 1995;62:407–413. doi: 10.1002/ijc.2910620409. [PubMed] [Cross Ref]
10. Yen T.W., Aardal N.P., Bronner M.P., Thorning D.R., Savard C.E., Lee S.P., Bell R.H., Jr. Myofibroblasts are responsible for the desmoplastic reaction surrounding human pancreatic carcinomas. Surgery. 2002;131:129–134. doi: 10.1067/msy.2002.119192. [PubMed] [Cross Ref]
11. Apte M.V., Park S., Phillips P.A., Santucci N., Goldstein D., Kumar R.K., Ramm G.A., Buchler M., Friess H., McCarroll J.A., Keogh G., Merrett N., Pirola R., Wilson J.S. Desmoplastic reaction in pancreatic cancer: Role of pancreatic stellate cells. Pancreas. 2004;29:179–187. doi: 10.1097/00006676-200410000-00002. [PubMed] [Cross Ref]
12. Yoshida S., Yokota T., Ujiki M., Ding X.Z., Pelham C., Adrian T.E., Talamonti M.S., Bell R.H., Jr., Denham W. Pancreatic cancer stimulates pancreatic stellate cell proliferation and TIMP-1 production through the MAP kinase pathway. Biochem. Biophys. Res. Commun. 2004;323:1241–1245. doi: 10.1016/j.bbrc.2004.08.229. [PubMed] [Cross Ref]
13. Bachem M.G., Schunemann M., Ramadani M., Siech M., Beger H., Buck A., Zhou S., Schmid-Kotsas A., Adler G. Pancreatic carcinoma cells induce fibrosis by stimulating proliferation and matrix synthesis of stellate cells. Gastroenterology. 2005;128:907–921. doi: 10.1053/j.gastro.2004.12.036. [PubMed] [Cross Ref]
14. Farrow B., Rowley D., Dang T., Berger D.H. Characterization of tumor-derived pancreatic stellate cells. J. Surg. Res. 2009;157:96–102. doi: 10.1016/j.jss.2009.03.064. [PubMed] [Cross Ref]
15. Saotome T., Inoue H., Fujimiya M., Fujiyama Y., Bamba T. Morphological and immunocytochemical identification of periacinar fibroblast-like cells derived from human pancreatic acini. Pancreas. 1997;14:373–382. doi: 10.1097/00006676-199705000-00008. [PubMed] [Cross Ref]
16. Apte M.V., Haber P.S., Applegate T.L., Norton I.D., McCaughan G.W., Korsten M.A., Pirola R.C., Wilson J.S. Periacinar stellate shaped cells in rat pancreas: Identification, isolation, and culture. Gut. 1998;43:128–133. doi: 10.1136/gut.43.1.128. [PMC free article] [PubMed] [Cross Ref]
17. Bachem M.G., Schneider E., Gross H., Weidenbach H., Schmid R.M., Menke A., Siech M., Beger H., Grunert A., Adler G. Identification, culture, and characterization of pancreatic stellate cells in rats and humans. Gastroenterology. 1998;115:421–432. doi: 10.1016/S0016-5085(98)70209-4. [PubMed] [Cross Ref]
18. Omary M.B., Lugea A., Lowe A.W., Pandol S.J. The pancreatic stellate cell: A star on the rise in pancreatic diseases. J. Clin. Invest. 2007;117:50–59. doi: 10.1172/JCI30082. [PMC free article] [PubMed] [Cross Ref]
19. Buchholz M., Kestler H.A., Holzmann K., Ellenrieder V., Schneiderhan W., Siech M., Adler G., Bachem M.G., Gress T.M. Transcriptome analysis of human hepatic and pancreatic stellate cells: Organ-specific variations of a common transcriptional phenotype. J. Mol. Med. 2005;83:795–805. doi: 10.1007/s00109-005-0680-2. [PubMed] [Cross Ref]
20. Friedman S.L. Stellate cells: A moving target in hepatic fibrogenesis. Hepatology. 2004;40:1041–1043. doi: 10.1002/hep.20476. [PubMed] [Cross Ref]
21. Gressner A.M., Bachem M.G. Molecular mechanisms of liver fibrogenesis--a homage to the role of activated fat-storing cells. Digestion. 1995;56:335–346. doi: 10.1159/000201257. [PubMed] [Cross Ref]
22. Watari N., Hotta Y., Mabuchi Y. Morphological studies on a vitamin A-storing cell and its complex with macrophage observed in mouse pancreatic tissues following excess vitamin A administration. Okajimas Folia Anat. Jpn. 1982;58:837–858. [PubMed]
23. Ikejiri N. The vitamin A-storing cells in the human and rat pancreas. Kurume Med. J. 1990;37:67–81. doi: 10.2739/kurumemedj.37.67. [PubMed] [Cross Ref]
24. Bachem M.G., Zhou S., Buck K., Schneiderhan W., Siech M. Pancreatic stellate cells--role in pancreas cancer. Langenbeck's archives of surgery/Deutsche Gesellschaft fur Chirurgie. 2008;393:891–900. doi: 10.1007/s00423-008-0279-5. [PubMed] [Cross Ref]
25. Siech M., Zhou Z., Zhou S., Bair B., Alt A., Hamm S., Gross H., Mayer J., Beger H.G., Tian X., Kornmann M., Bachem M.G. Stimulation of stellate cells by injured acinar cells: A model of acute pancreatitis induced by alcohol and fat (VLDL) Am. J. Physiol. Gastrointest. Liver Physiol. 2009;297:G1163–G1171. [PubMed]
26. Phillips P.A., McCarroll J.A., Park S., Wu M.J., Pirola R., Korsten M., Wilson J.S., Apte M.V. Rat pancreatic stellate cells secrete matrix metalloproteinases: Implications for extracellular matrix turnover. Gut. 2003;52:275–282. doi: 10.1136/gut.52.2.275. [PMC free article] [PubMed] [Cross Ref]
27. Bachem M.G., Zhou Z., Zhou S., Siech M. Role of stellate cells in pancreatic fibrogenesis associated with acute and chronic pancreatitis. J. Gastroenterol. Hepatol. 2006;21:S92–96. doi: 10.1111/j.1440-1746.2006.04592.x. [PubMed] [Cross Ref]
28. Sparmann G., Glass A., Brock P., Jaster R., Koczan D., Thiesen H.J., Liebe S., Emmrich J. Inhibition of lymphocyte apoptosis by pancreatic stellate cells: Impact of interleukin-15. Am. J. Physiol. Gastrointest. Liver Physiol. 2005;289:G842–851. doi: 10.1152/ajpgi.00483.2004. [PubMed] [Cross Ref]
29. Marrache F., Pendyala S., Bhagat G., Betz K.S., Song Z., Wang T.C. Role of bone marrow-derived cells in experimental chronic pancreatitis. Gut. 2008;57:1113–1120. doi: 10.1136/gut.2007.143271. [PubMed] [Cross Ref]
30. Watanabe A., Yoneda M., Ikeda F., Terao-Muto Y., Sato H., Kai C. CD147/EMMPRIN acts as a functional entry receptor for measles virus on epithelial cells. J. Virol. 2010;84:4183–4193. doi: 10.1128/JVI.02168-09. [PMC free article] [PubMed] [Cross Ref]
31. Kordes C., Sawitza I., Haussinger D. Hepatic and pancreatic stellate cells in focus. Biol. Chem. 2009;390:1003–1012. [PubMed]
32. Mato E., Lucas M., Petriz J., Gomis R., Novials A. Identification of a pancreatic stellate cell population with properties of progenitor cells: New role for stellate cells in the pancreas. Biochem. J. 2009;421:181–191. doi: 10.1042/BJ20081466. [PubMed] [Cross Ref]
33. Pan J.J., Oh S.H., Lee W.C., Petersen B.E. Bone marrow-derived progenitor cells could modulate pancreatic cancer tumorigenesis via peritumoral microenvironment in a rat model. Oncol. Res. 2009;17:339–345. doi: 10.3727/096504009788428424. [PMC free article] [PubMed] [Cross Ref]
34. Guerra C., Schuhmacher A.J., Canamero M., Grippo P.J., Verdaguer L., Perez-Gallego L., Dubus P., Sandgren E.P., Barbacid M. Chronic pancreatitis is essential for induction of pancreatic ductal adenocarcinoma by K-Ras oncogenes in adult mice. Cancer Cell. 2007;11:291–302. [PubMed]
35. Lowenfels A.B., Maisonneuve P., Cavallini G., Ammann R.W., Lankisch P.G., Andersen J.R., Dimagno E.P., Andren-Sandberg A., Domellof L. Pancreatitis and the risk of pancreatic cancer. International Pancreatitis Study Group. N. Engl. J. Med. 1993;328:1433–1437. doi: 10.1056/NEJM199305203282001. [PubMed] [Cross Ref]
36. Malka D., Hammel P., Maire F., Rufat P., Madeira I., Pessione F., Levy P., Ruszniewski P. Risk of pancreatic adenocarcinoma in chronic pancreatitis. Gut. 2002;51:849–852. doi: 10.1136/gut.51.6.849. [PMC free article] [PubMed] [Cross Ref]
37. Carriere C., Young A.L., Gunn J.R., Longnecker D.S., Korc M. Acute pancreatitis markedly accelerates pancreatic cancer progression in mice expressing oncogenic Kras. Biochem. Biophys. Res. Commun. 2009;382:561–565. doi: 10.1016/j.bbrc.2009.03.068. [PMC free article] [PubMed] [Cross Ref]
38. Nakashima H., Nakamura M., Yamaguchi H., Yamanaka N., Akiyoshi T., Koga K., Yamaguchi K., Tsuneyoshi M., Tanaka M., Katano M. Nuclear factor-kappaB contributes to hedgehog signaling pathway activation through sonic hedgehog induction in pancreatic cancer. Cancer Res. 2006;66:7041–7049. doi: 10.1158/0008-5472.CAN-05-4588. [PubMed] [Cross Ref]
39. Pasca di Magliano M., Sekine S., Ermilov A., Ferris J., Dlugosz A.A., Hebrok M. Hedgehog/Ras interactions regulate early stages of pancreatic cancer. Genes Dev. 2006;20:3161–3173. doi: 10.1101/gad.1470806. [PubMed] [Cross Ref]
40. Thayer S.P., di Magliano M.P., Heiser P.W., Nielsen C.M., Roberts D.J., Lauwers G.Y., Qi Y.P., Gysin S., Fernandez-del Castillo C., Yajnik V., Antoniu B., McMahon M., Warshaw A.L., Hebrok M. Hedgehog is an early and late mediator of pancreatic cancer tumorigenesis. Nature. 2003;425:851–856. doi: 10.1038/nature02009. [PMC free article] [PubMed] [Cross Ref]
41. De La O.J., Emerson L.L., Goodman J.L., Froebe S.C., Illum B.E., Curtis A.B., Murtaugh L.C. Notch and Kras reprogram pancreatic acinar cells to ductal intraepithelial neoplasia. Proc. Natl. Acad. Sci. USA. 2008;105:18907–18912. [PubMed]
42. Miyamoto Y., Maitra A., Ghosh B., Zechner U., Argani P., Iacobuzio-Donahue C.A., Sriuranpong V., Iso T., Meszoely I.M., Wolfe M.S., Hruban R.H., Ball D.W., Schmid R.M., Leach S.D. Notch mediates TGF alpha-induced changes in epithelial differentiation during pancreatic tumorigenesis. Cancer Cell. 2003;3:565–576. doi: 10.1016/S1535-6108(03)00140-5. [PubMed] [Cross Ref]
43. Siveke J.T., Einwachter H., Sipos B., Lubeseder-Martellato C., Kloppel G., Schmid R.M. Concomitant pancreatic activation of Kras(G12D) and Tgfa results in cystic papillary neoplasms reminiscent of human IPMN. Cancer Cell. 2007;12:266–279. doi: 10.1016/j.ccr.2007.08.002. [PubMed] [Cross Ref]
44. Erkan M., Michalski C.W., Rieder S., Reiser-Erkan C., Abiatari I., Kolb A., Giese N.A., Esposito I., Friess H., Kleeff J. The activated stroma index is a novel and independent prognostic marker in pancreatic ductal adenocarcinoma. Clin. Gastroenterol. Hepatol. 2008;6:1155–1161. doi: 10.1016/j.cgh.2008.05.006. [PubMed] [Cross Ref]
45. Bonner-Weir S., Sharma A. Pancreatic stem cells. J. Pathol. 2002;197:519–526. doi: 10.1002/path.1158. [PubMed] [Cross Ref]
46. Esposito I., Seiler C., Bergmann F., Kleeff J., Friess H., Schirmacher P. Hypothetical progression model of pancreatic cancer with origin in the centroacinar-acinar compartment. Pancreas. 2007;35:212–217. doi: 10.1097/mpa.0b013e31805d0190. [PubMed] [Cross Ref]
47. Stanger B.Z., Stiles B., Lauwers G.Y., Bardeesy N., Mendoza M., Wang Y., Greenwood A., Cheng K.H., McLaughlin M., Brown D., Depinho R.A., Wu H., Melton D.A., Dor Y. Pten constrains centroacinar cell expansion and malignant transformation in the pancreas. Cancer Cell. 2005;8:185–195. doi: 10.1016/j.ccr.2005.07.015. [PubMed] [Cross Ref]
48. Habbe N., Shi G., Meguid R.A., Fendrich V., Esni F., Chen H., Feldmann G., Stoffers D.A., Konieczny S.F., Leach S.D., Maitra A. Spontaneous induction of murine pancreatic intraepithelial neoplasia (mPanIN) by acinar cell targeting of oncogenic Kras in adult mice. Proc. Natl. Acad. Sci. USA. 2008;105:18913–18918. doi: 10.1073/pnas.0810097105. [PubMed] [Cross Ref]
49. Morris J.P.T., Cano D.A., Sekine S., Wang S.C., Hebrok M. Beta-catenin blocks Kras-dependent reprogramming of acini into pancreatic cancer precursor lesions in mice. J. Clin. Invest. 2010;120:508–520. doi: 10.1172/JCI40045. [PMC free article] [PubMed] [Cross Ref]
50. Zhu L., Shi G., Schmidt C.M., Hruban R.H., Konieczny S.F. Acinar cells contribute to the molecular heterogeneity of pancreatic intraepithelial neoplasia. Am. J. Pathol. 2007;171:263–273. doi: 10.2353/ajpath.2007.061176. [PubMed] [Cross Ref]
51. Vonlaufen A., Phillips P.A., Xu Z., Goldstein D., Pirola R.C., Wilson J.S., Apte M.V. Pancreatic stellate cells and pancreatic cancer cells: An unholy alliance. Cancer Res. 2008;68:7707–7710. doi: 10.1158/0008-5472.CAN-08-1132. [PubMed] [Cross Ref]
52. Koenig A., Mueller C., Hasel C., Adler G., Menke A. Collagen type I induces disruption of E-cadherin-mediated cell-cell contacts and promotes proliferation of pancreatic carcinoma cells. Cancer Res. 2006;66:4662–4671. doi: 10.1158/0008-5472.CAN-05-2804. [PubMed] [Cross Ref]
53. Shintani Y., Hollingsworth M.A., Wheelock M.J., Johnson K.R. Collagen I promotes metastasis in pancreatic cancer by activating c-Jun NH(2)-terminal kinase 1 and up-regulating N-cadherin expression. Cancer Res. 2006;66:11745–11753. doi: 10.1158/0008-5472.CAN-06-2322. [PubMed] [Cross Ref]
54. Tahara J., Shimizu K., Shiratori K. Engulfment of necrotic acinar cells by pancreatic stellate cells inhibits pancreatic fibrogenesis. Pancreas. 2008;37:69–74. doi: 10.1097/MPA.0b013e318160a5cb. [PubMed] [Cross Ref]
55. Morishita K., Shimizu K., Haruta I., Kawamura S., Kobayashi M., Shiratori K. Engulfment of Gram-Positive Bacteria by Pancreatic Stellate Cells in Pancreatic Fibrosis. Pancreas. 2010 doi: 10.1097/MPA.0b013e3181d7ace1. [PubMed] [Cross Ref]
56. Lowenfels A.B., Maisonneuve P. Risk factors for pancreatic cancer. J. Cell Biochem. 2005;95:649–656. doi: 10.1002/jcb.20461. [PubMed] [Cross Ref]
57. Farrow B., Albo D., Berger D.H. The role of the tumor microenvironment in the progression of pancreatic cancer. J. Surg. Res. 2008;149:319–328. doi: 10.1016/j.jss.2007.12.757. [PubMed] [Cross Ref]
58. Hanahan D., Weinberg R.A. The hallmarks of cancer. Cell. 2000;100:57–70. doi: 10.1016/S0092-8674(00)81683-9. [PubMed] [Cross Ref]
59. Liotta L.A., Kohn E.C. The microenvironment of the tumour-host interface. Nature. 2001;411:375–379. doi: 10.1038/35077241. [PubMed] [Cross Ref]
60. Wernert N. The multiple roles of tumour stroma. Virchows Arch. 1997;430:433–443. doi: 10.1007/s004280050053. [PubMed] [Cross Ref]
61. Ramachandran V., Arumugam T., Langley R., Hwang R.F., Vivas-Mejia P., Sood A.K., Lopez-Berestein G., Logsdon C.D. The ADMR receptor mediates the effects of adrenomedullin on pancreatic cancer cells and on cells of the tumor microenvironment. PloS ONE. 2009;4:e7502. doi: 10.1371/journal.pone.0007502. [PMC free article] [PubMed] [Cross Ref]
62. Farrow B., Berger D.H., Rowley D. Tumor-derived pancreatic stellate cells promote pancreatic cancer cell invasion through release of thrombospondin-2. J. Surg. Res. 2009;156:155–160. doi: 10.1016/j.jss.2009.03.040. [PubMed] [Cross Ref]
63. Schneiderhan W., Diaz F., Fundel M., Zhou S., Siech M., Hasel C., Moller P., Gschwend J.E., Seufferlein T., Gress T., Adler G., Bachem M.G. Pancreatic stellate cells are an important source of MMP-2 in human pancreatic cancer and accelerate tumor progression in a murine xenograft model and CAM assay. J. Cell Sci. 2007;120:512–519. doi: 10.1242/jcs.03347. [PubMed] [Cross Ref]
64. Keleg S., Buchler P., Ludwig R., Buchler M.W., Friess H. Invasion and metastasis in pancreatic cancer. Mol. Cancer. 2003;2:14. doi: 10.1186/1476-4598-2-14. [PMC free article] [PubMed] [Cross Ref]
65. Bacac M., Stamenkovic I. Metastatic cancer cell. Ann. Rev. Pathol. 2008;3:221–247. doi: 10.1146/annurev.pathmechdis.3.121806.151523. [PubMed] [Cross Ref]
66. Zucker S., Cao J., Chen W.T. Critical appraisal of the use of matrix metalloproteinase inhibitors in cancer treatment. Oncogene. 2000;19:6642–6650. doi: 10.1038/sj.onc.1204097. [PubMed] [Cross Ref]
67. Overall C.M., Kleifeld O. Towards third generation matrix metalloproteinase inhibitors for cancer therapy. Br. J. Cancer. 2006;94:941–946. doi: 10.1038/sj.bjc.6603043. [PMC free article] [PubMed] [Cross Ref]
68. Zucker S., Cao J. Selective matrix metalloproteinase (MMP) inhibitors in cancer therapy: Ready for prime time? Cancer Biol. Ther. 2009;8:2371–2373. doi: 10.4161/cbt.8.24.10353. [PMC free article] [PubMed] [Cross Ref]
69. Zhang W., Erkan M., Abiatari I., Giese N.A., Felix K., Kayed H., Buchler M.W., Friess H., Kleeff J. Expression of extracellular matrix metalloproteinase inducer (EMMPRIN/CD147) in pancreatic neoplasm and pancreatic stellate cells. Cancer Biol. Ther. 2007;6:218–227. doi: 10.4161/cbt.6.2.3623. [PubMed] [Cross Ref]
70. Dang D., Atakilit A., Ramos D.M. EMMPRIN modulates migration and deposition of TN-C in oral squamous carcinoma. Anticancer Res. 2008;28:2049–2054. [PubMed]
71. Hanata K., Yamaguchi N., Yoshikawa K., Mezaki Y., Miura M., Suzuki S., Senoo H., Ishikawa K. Soluble EMMPRIN (extra-cellular matrix metalloproteinase inducer) stimulates the migration of HEp-2 human laryngeal carcinoma cells, accompanied by increased MMP-2 production in fibroblasts. Arch. Histol. Cytol. 2007;70:267–277. doi: 10.1679/aohc.70.267. [PubMed] [Cross Ref]
72. Kanekura T., Chen X., Kanzaki T. Basigin (CD147) is expressed on melanoma cells and induces tumor cell invasion by stimulating production of matrix metalloproteinases by fibroblasts. Int. J. Cancer. 2002;99:520–528. doi: 10.1002/ijc.10390. [PubMed] [Cross Ref]
73. Qian A.R., Zhang W., Cao J.P., Yang P.F., Gao X., Wang Z., Xu H.Y., Weng Y.Y., Shang P. Downregulation of CD147 expression alters cytoskeleton architecture and inhibits gelatinase production and SAPK pathway in human hepatocellular carcinoma cells. J. Exp. Clin. Cancer Res. 2008;27:50. doi: 10.1186/1756-9966-27-50. [PMC free article] [PubMed] [Cross Ref]
74. Marieb E.A., Zoltan-Jones A., Li R., Misra S., Ghatak S., Cao J., Zucker S., Toole B.P. Emmprin promotes anchorage-independent growth in human mammary carcinoma cells by stimulating hyaluronan production. Cancer Res. 2004;64:1229–1232. doi: 10.1158/0008-5472.CAN-03-2832. [PubMed] [Cross Ref]
75. Yang J.M., O'Neill P., Jin W., Foty R., Medina D.J., Xu Z., Lomas M., Arndt G.M., Tang Y., Nakada M., Yan L., Hait W.N. Extracellular matrix metalloproteinase inducer (CD147) confers resistance of breast cancer cells to Anoikis through inhibition of Bim. J. Biol. Chem. 2006;281:9719–9727. [PubMed]
76. Tang Y., Nakada M.T., Kesavan P., McCabe F., Millar H., Rafferty P., Bugelski P., Yan L. Extracellular matrix metalloproteinase inducer stimulates tumor angiogenesis by elevating vascular endothelial cell growth factor and matrix metalloproteinases. Cancer Res. 2005;65:3193–3199. [PubMed]
77. Voigt H., Vetter-Kauczok C.S., Schrama D., Hofmann U.B., Becker J.C., Houben R. CD147 impacts angiogenesis and metastasis formation. Cancer Invest. 2009;27:329–333. doi: 10.1080/07357900802392675. [PubMed] [Cross Ref]
78. Zheng H.C., Takahashi H., Murai Y., Cui Z.G., Nomoto K., Miwa S., Tsuneyama K., Takano Y. Upregulated EMMPRIN/CD147 might contribute to growth and angiogenesis of gastric carcinoma: A good marker for local invasion and prognosis. Br. J. Cancer. 2006;95:1371–1378. doi: 10.1038/sj.bjc.6603425. [PMC free article] [PubMed] [Cross Ref]
79. Li Q.Q., Wang W.J., Xu J.D., Cao X.X., Chen Q., Yang J.M., Xu Z.D. Involvement of CD147 in regulation of multidrug resistance to P-gp substrate drugs and in vitro invasion in breast cancer cells. Cancer Sci. 2007;98:1064–1069. doi: 10.1111/j.1349-7006.2007.00487.x. [PubMed] [Cross Ref]
80. Toole B.P., Slomiany M.G. Hyaluronan, CD44 and Emmprin: Partners in cancer cell chemoresistance. Drug Resist. Update. 2008;11:110–121. doi: 10.1016/j.drup.2008.04.002. [PMC free article] [PubMed] [Cross Ref]
81. Nabeshima K., Iwasaki H., Koga K., Hojo H., Suzumiya J., Kikuchi M. Emmprin (basigin/CD147): Matrix metalloproteinase modulator and multifunctional cell recognition molecule that plays a critical role in cancer progression. Pathol. Int. 2006;56:359–367. doi: 10.1111/j.1440-1827.2006.01972.x. [PubMed] [Cross Ref]
82. Schneiderhan W., Scheler M., Holzmann K.H., Marx M., Gschwend J.E., Buchholz M., Gress T.M., Adler G., Seufferlein T., Oswald F. CD147 Silencing Inhibits Lactate Transport and Reduces Malignant Potential of pancreatic cancer cells in in vivo and in vitro Models. Gut. 2009;58:1391–1398. doi: 10.1136/gut.2009.181412. [PubMed] [Cross Ref]
83. Dalberg K., Eriksson E., Enberg U., Kjellman M., Backdahl M. Gelatinase A, membrane type 1 matrix metalloproteinase, and extracellular matrix metalloproteinase inducer mRNA expression: Correlation with invasive growth of breast cancer. World J. Surg. 2000;24:334–340. doi: 10.1007/s002689910053. [PubMed] [Cross Ref]
84. Zhong W.D., Han Z.D., He H.C., Bi X.C., Dai Q.S., Zhu G., Ye Y.K., Liang Y.X., Qin W.J., Zhang Z., Zeng G.H., Chen Z.N. CD147, MMP-1, MMP-2 and MMP-9 protein expression as significant prognostic factors in human prostate cancer. Oncology. 2008;75:230–236. doi: 10.1159/000163852. [PubMed] [Cross Ref]
85. Li R., Huang L., Guo H., Toole B.P. Basigin (murine EMMPRIN) stimulates matrix metalloproteinase production by fibroblasts. J. Cell Physiol. 2001;186:371–379. doi: 10.1002/1097-4652(2000)9999:999<000::AID-JCP1042>3.0.CO;2-8. [PubMed] [Cross Ref]
86. Sun J., Hemler M.E. Regulation of MMP-1 and MMP-2 production through CD147/ extracellular matrix metalloproteinase inducer interactions. Cancer Res. 2001;61:2276–2281. [PubMed]
87. Tang Y., Kesavan P., Nakada M.T., Yan L. Tumor-stroma interaction: Positive feedback regulation of extracellular matrix metalloproteinase inducer (EMMPRIN) expression and matrix metalloproteinase-dependent generation of soluble EMMPRIN. Mol. Cancer Res. 2004;2:73–80. [PubMed]
88. Chen X., Lin J., Kanekura T., Su J., Lin W., Xie H., Wu Y., Li J., Chen M., Chang J. A small interfering CD147-targeting RNA inhibited the proliferation, invasiveness, and metastatic activity of malignant melanoma. Cancer Res. 2006;66:11323–11330. doi: 10.1158/0008-5472.CAN-06-1536. [PubMed] [Cross Ref]
89. Dean N.R., Newman J.R., Helman E.E., Zhang W., Safavy S., Weeks D.M., Cunningham M., Snyder L.A., Tang Y., Yan L., McNally L.R., Buchsbaum D.J., Rosenthal E.L. Anti-EMMPRIN monoclonal antibody as a novel agent for therapy of head and neck cancer. Clin. Cancer Res. 2009;15:4058–4065. doi: 10.1158/1078-0432.CCR-09-0212. [PMC free article] [PubMed] [Cross Ref]
90. Voigt H., Houben R., Schrama D., Hofmann U.B., Vetter-Kauczok C.S., Becker J.C. Matrix metalloproteinase induction in the tumor stroma does not depend on CD147 expression in murine B16 melanoma. Tumour Biol. 2007;28:229–237. [PubMed]
91. Tang W., Chang S.B., Hemler M.E. Links between CD147 function, glycosylation, and caveolin-1. Mol. Biol. Cell. 2004;15:4043–4050. doi: 10.1091/mbc.E04-05-0402. [PMC free article] [PubMed] [Cross Ref]
92. Millimaggi D., Mari M., D'Ascenzo S., Carosa E., Jannini E.A., Zucker S., Carta G., Pavan A., Dolo V. Tumor vesicle-associated CD147 modulates the angiogenic capability of endothelial cells. Neoplasia N. Y. 2007;9:349–357. doi: 10.1593/neo.07133. [PMC free article] [PubMed] [Cross Ref]
93. Sidhu S.S., Mengistab A.T., Tauscher A.N., LaVail J., Basbaum C. The microvesicle as a vehicle for EMMPRIN in tumor-stromal interactions. Oncogene. 2004;23:956–963. doi: 10.1038/sj.onc.1207070. [PubMed] [Cross Ref]
94. Haug C., Lenz C., Diaz F., Bachem M.G. Oxidized low-density lipoproteins stimulate extracellular matrix metalloproteinase Inducer (EMMPRIN) release by coronary smooth muscle cells. Arterioscler. Thromb. Vasc. Biol. 2004;24:1823–1829. doi: 10.1161/01.ATV.0000142806.59283.11. [PubMed] [Cross Ref]
95. Belton R.J., Jr., Chen L., Mesquita F.S., Nowak R.A. Basigin-2 is a cell surface receptor for soluble basigin ligand. J. Biol. Chem. 2008;283:17805–17814. [PubMed]
96. Lim M., Martinez T., Jablons D., Cameron R., Guo H., Toole B., Li J.D., Basbaum C. Tumor-derived EMMPRIN (extracellular matrix metalloproteinase inducer) stimulates collagenase transcription through MAPK p38. FEBS Lett. 1998;441:88–92. doi: 10.1016/S0014-5793(98)01474-4. [PubMed] [Cross Ref]
97. Taylor P.M., Woodfield R.J., Hodgkin M.N., Pettitt T.R., Martin A., Kerr D.J., Wakelam M.J. Breast cancer cell-derived EMMPRIN stimulates fibroblast MMP2 release through a phospholipase A(2) and 5-lipoxygenase catalyzed pathway. Oncogene. 2002;21:5765–5772. doi: 10.1038/sj.onc.1205702. [PubMed] [Cross Ref]
98. Warburg O. On the origin of cancer cells. Science. 1956;123:309–314. [PubMed]
99. Guo H., Li R., Zucker S., Toole B.P. EMMPRIN (CD147), an inducer of matrix metalloproteinase synthesis, also binds interstitial collagenase to the tumor cell surface. Cancer Res. 2000;60:888–891. [PubMed]
100. Sternlicht M.D., Werb Z. How matrix metalloproteinases regulate cell behavior. Annu. Rev. Cell. Dev. Biol. 2001;17:463–516. doi: 10.1146/annurev.cellbio.17.1.463. [PMC free article] [PubMed] [Cross Ref]
101. Bramhall S.R., Neoptolemos J.P., Stamp G.W., Lemoine N.R. Imbalance of expression of matrix metalloproteinases (MMPs) and tissue inhibitors of the matrix metalloproteinases (TIMPs) in human pancreatic carcinoma. J. Pathol. 1997;182:347–355. doi: 10.1002/(SICI)1096-9896(199707)182:3<347::AID-PATH848>3.0.CO;2-J. [PubMed] [Cross Ref]
102. Hwang R.F., Moore T., Arumugam T., Ramachandran V., Amos K.D., Rivera A., Ji B., Evans D.B., Logsdon C.D. Cancer-associated stromal fibroblasts promote pancreatic tumor progression. Cancer Res. 2008;68:918–926. doi: 10.1158/0008-5472.CAN-07-5714. [PMC free article] [PubMed] [Cross Ref]
103. Gao Z., Wang X., Wu K., Zhao Y., Hu G. Pancreatic stellate cells increase the invasion of human pancreatic cancer cells through the stromal cell-derived factor-1/CXCR4 axis. Pancreatology. 2010;10:186–193. doi: 10.1159/000236012. [PubMed] [Cross Ref]
104. Vonlaufen A., Joshi S., Qu C., Phillips P.A., Xu Z., Parker N.R., Toi C.S., Pirola R.C., Wilson J.S., Goldstein D., Apte M.V. Pancreatic stellate cells: Partners in crime with pancreatic cancer cells. Cancer Res. 2008;68:2085–2093. doi: 10.1158/0008-5472.CAN-07-2477. [PubMed] [Cross Ref]
105. Fujita H., Ohuchida K., Mizumoto K., Egami T., Miyoshi K., Moriyama T., Cui L., Yu J., Zhao M., Manabe T., Tanaka M. Tumor-stromal interactions with direct cell contacts enhance proliferation of human pancreatic carcinoma cells. Cancer Sci. 2009;100:2309–2317. doi: 10.1111/j.1349-7006.2009.01317.x. [PubMed] [Cross Ref]
106. Korc M. Pancreatic cancer-associated stroma production. Am. J. Surg. 2007;194:S84–86. doi: 10.1016/j.amjsurg.2007.05.004. [PMC free article] [PubMed] [Cross Ref]
107. Giovannetti E., Del Tacca M., Mey V., Funel N., Nannizzi S., Ricci S., Orlandini C., Boggi U., Campani D., Del Chiaro M., Iannopollo M., Bevilacqua G., Mosca F., Danesi R. Transcription analysis of human equilibrative nucleoside transporter-1 predicts survival in pancreas cancer patients treated with gemcitabine. Cancer Res. 2006;66:3928–3935. doi: 10.1158/0008-5472.CAN-05-4203. [PubMed] [Cross Ref]
108. Giovannetti E., Mey V., Nannizzi S., Pasqualetti G., Del Tacca M., Danesi R. Pharmacogenetics of anticancer drug sensitivity in pancreatic cancer. Mol. Cancer Ther. 2006;5:1387–1395. doi: 10.1158/1535-7163.MCT-06-0004. [PubMed] [Cross Ref]
109. Shi X., Liu S., Kleeff J., Friess H., Buchler M.W. Acquired resistance of pancreatic cancer cells towards 5-Fluorouracil and gemcitabine is associated with altered expression of apoptosis-regulating genes. Oncology. 2002;62:354–362. doi: 10.1159/000065068. [PubMed] [Cross Ref]
110. Wang C.Y., Cusack J.C., Jr., Liu R., Baldwin A.S., Jr. Control of inducible chemoresistance: Enhanced anti-tumor therapy through increased apoptosis by inhibition of NF-kappaB. Nature Medicine. 1999;5:412–417. doi: 10.1038/7410. [PubMed] [Cross Ref]
111. Arlt A., Vorndamm J., Breitenbroich M., Folsch U.R., Kalthoff H., Schmidt W.E., Schafer H. Inhibition of NF-kappaB sensitizes human pancreatic carcinoma cells to apoptosis induced by etoposide (VP16) or doxorubicin. Oncogene. 2001;20:859–868. doi: 10.1038/sj.onc.1204168. [PubMed] [Cross Ref]
112. Muerkoster S., Wegehenkel K., Arlt A., Witt M., Sipos B., Kruse M.L., Sebens T., Kloppel G., Kalthoff H., Folsch U.R., Schafer H. Tumor stroma interactions induce chemoresistance in pancreatic ductal carcinoma cells involving increased secretion and paracrine effects of nitric oxide and interleukin-1beta. Cancer Res. 2004;64:1331–1337. doi: 10.1158/0008-5472.CAN-03-1860. [PubMed] [Cross Ref]
113. Muerkoster S.S., Werbing V., Koch D., Sipos B., Ammerpohl O., Kalthoff H., Tsao M.S., Folsch U.R., Schafer H. Role of myofibroblasts in innate chemoresistance of pancreatic carcinoma--epigenetic downregulation of caspases. Int. J. Cancer. 2008;123:1751–1760. doi: 10.1002/ijc.23703. [PubMed] [Cross Ref]
114. Miyamoto H., Murakami T., Tsuchida K., Sugino H., Miyake H., Tashiro S. Tumor-stroma interaction of human pancreatic cancer: Acquired resistance to anticancer drugs and proliferation regulation is dependent on extracellular matrix proteins. Pancreas. 2004;28:38–44. doi: 10.1097/00006676-200401000-00006. [PubMed] [Cross Ref]
115. Tannock I.F., Lee C.M., Tunggal J.K., Cowan D.S., Egorin M.J. Limited penetration of anticancer drugs through tumor tissue: A potential cause of resistance of solid tumors to chemotherapy. Clin. Cancer Res. 2002;8:878–884. [PubMed]
116. Stander M., Naumann U., Wick W., Weller M. Transforming growth factor-beta and p-21: Multiple molecular targets of decorin-mediated suppression of neoplastic growth. Cell Tissue Res. 1999;296:221–227. doi: 10.1007/s004410051283. [PubMed] [Cross Ref]
117. Koninger J., Giese N.A., di Mola F.F., Berberat P., Giese T., Esposito I., Bachem M.G., Buchler M.W., Friess H. Overexpressed decorin in pancreatic cancer: Potential tumor growth inhibition and attenuation of chemotherapeutic action. Clin. Cancer. Res. 2004;10:4776–4783. doi: 10.1158/1078-0432.CCR-1190-03. [PubMed] [Cross Ref]
118. Olive K.P., Jacobetz M.A., Davidson C.J., Gopinathan A., McIntyre D., Honess D., Madhu B., Goldgraben M.A., Caldwell M.E., Allard D., Frese K.K., Denicola G., Feig C., Combs C., Winter S.P., Ireland-Zecchini H., Reichelt S., Howat W.J., Chang A., Dhara M., Wang L., Ruckert F., Grutzmann R., Pilarsky C., Izeradjene K., Hingorani S.R., Huang P., Davies S.E., Plunkett W., Egorin M., Hruban R.H., Whitebread N., McGovern K., Adams J., Iacobuzio-Donahue C., Griffiths J., Tuveson D.A. Inhibition of Hedgehog signaling enhances delivery of chemotherapy in a mouse model of pancreatic cancer. Science. 2009;324:1457–1461. doi: 10.1126/science.1171362. [PMC free article] [PubMed] [Cross Ref]
119. Kim N., Choi S., Lim C., Lee H., Oh J. Albumin mediates PPAR-gamma or C/EBP-alpha-induced phenotypic changes in pancreatic stellate cells. Biochem. Biophys. Res. Commun. 2010;391:640–644. doi: 10.1016/j.bbrc.2009.11.112. [PubMed] [Cross Ref]

Articles from Cancers are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)