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Tumors are characterized by extracellular matrix (ECM) remodeling and stiffening. The importance of ECM remodeling to cancer is appreciated; the relevance of stiffening is less clear. We found that breast tumorigenesis is accompanied by collagen crosslinking, ECM stiffening and increased focal adhesions. Inducing collagen crosslinking stiffened the ECM, promoted focal adhesions, enhanced PI3 Kinase (PI3K) activity, and induced the invasion of an oncogene-initiated epithelium. Inhibiting integrin signaling repressed the invasion of a premalignant epithelium into a stiffened, crosslinked ECM, and forced integrin clustering promoted focal adhesions, enhanced PI3K signaling and induced the invasion of a premalignant epithelium. Consistently, reducing lysyl oxidase-mediated collagen crosslinking prevented MMTV-Neu-induced fibrosis, decreased focal adhesions and PI3K activity, impeded malignancy and lowered tumor incidence. These data show how collagen crosslinking can modulate tissue fibrosis and stiffness to force focal adhesions, growth factor signaling and breast malignancy.
The tumor stroma is characterized by extracellular matrix (ECM) remodeling and stiffening and tissue stiffness has been exploited to detect cancer (Butcher et al., 2009; Sinkus et al., 2000). ECM stiffness enhances cell growth and survival and promotes migration (Lo et al., 2000), and ECM rigidity disrupts tissue morphogenesis by increasing cell tension (Paszek et al., 2005). Reducing cell tension repressed the malignant behavior of mammary epithelial cells (MECs) and normalized the behavior of breast cancer cells in culture (Paszek et al., 2005). What drives ECM stiffening in tumors and whether ECM tension could drive tumor progression has yet to be determined.
Collagen is the most abundant ECM scaffolding protein in the stroma and contributes significantly to the tensile strength of tissue (Kolacna et al., 2007). Collagen metabolism is deregulated in cancer, where increased collagen expression, elevated deposition, altered organization, and enhanced matrix metalloproteinase (MMP) activity and collagen turnover have been implicated in tumor progression (Jodele et al., 2006). MMP-mediated collagen remodeling can create space for cells to migrate, produce substrate cleavage fragments with independent biological activity, modify adhesion to regulate tissue architecture, and activate, deactivate, or alter the activity of signaling molecules (Page-McCaw et al., 2007). Although high levels of MMPs correlate with poor prognosis in cancer patients (Tetu et al., 2006), and modulating MMP activity changes tumor phenotype (Zhang et al., 2008), MMP inhibitors failed clinically (Coussens et al., 2002), indicating other ECM remodeling parameters regulate malignancy.
Type I collagen is considered a structural barrier against tumor invasion, paradoxically, increased expression of collagen is associated with elevated incidence of metastasis (Ramaswamy et al., 2003). Indeed, mammographic density, which is characterized by higher collagen I, increases breast cancer risk (Martin and Boyd, 2008). Importantly, collagen crosslinking accompanies tissue fibrosis (van der Slot et al., 2005) and fibrosis increases risk to malignancy (Colpaert et al., 2003). Lysyl oxidase (LOX), a copper-dependent amine oxidase (Kagan and Li 2003) which initiates the process of covalent intra- and intermolecular crosslinking of collagen by oxidatively deaminating specific lysine and hydroxylysine residues located in the telopeptide domains (Yamauchi and Shiiba, 2008), is frequently elevated in tumors (Erler et al., 2009). Active LOX stiffens tissues and can compromise their function (Pfeiffer et al., 2005) and reducing LOX activity tempers tissue stiffness and prevents fibrosis (Georges et al., 2007). Nevertheless, the relationship between collagen crosslinking, tissue fibrosis and tension and cancer has yet to be assessed.
Integrins transduce cues from the ECM by assembling adhesion plaque complexes that initiate biochemical signaling and stimulate cytoskeletal remodeling to regulate cell behavior (Miranti and Brugge, 2002). Force increases integrin expression, activity and focal adhesions (Paszek et al., 2005; Sawada et al., 2006). Human breast tumors are often fibrotic and stiff, and breast cancer cells that exhibit high tension have elevated integrins and focal adhesions and increased integrin signaling (Madan et al., 2006; Mitra and Schlaepfer, 2006). Thus ECM stiffness could regulate malignancy by enhancing integrin-dependent mechanotransduction. Consistently, breast malignancy can be inhibited by genetically ablating integrin expression (White et al., 2004), and breast cancer cell behavior can be repressed by inhibiting integrin activity or reducing cell tension (Paszek et al., 2005). Likewise, knocking down the expression or inhibiting the function of focal adhesion kinase (FAK) or p130Cas, two integrin adhesion proteins, impedes breast tumor progression (Cabodi et al., 2006; Lahlou et al., 2007). Here, we asked if collagen crosslinking could stiffen the ECM and induce fibrosis to promote breast malignancy by altering integrins and whether inhibiting collagen crosslinking could prevent fibrosis and impede breast tumorigenesis by reducing integrin signaling.
The HER2 gene is a member of the epidermal growth factor receptor (EGFR) family that is amplified in 20-25% of human breast cancers. The murine equivalent of HER2 is the wild type Neu transgene which under the MMTV promoter (MMTV–Neu) develops breast tumors with a long latency (Kim and Muller, 1999). Using the MMTV-Neu model we studied the relationship between tissue fibrosis, stiffness and cancer. Unconfined compression and rheological testing showed an incremental stiffening of the mammary gland as it transitioned from normal to premalignant to invasive cancer (Fig 1A, B & C top) and demonstrated that the stromal tissue adjacent to the invading epithelium was also substantially stiffer than normal. Total levels (Supp Fig 1) and amount of fibrillar collagen increased markedly (Fig 1C & D) and second harmonics generation (SHG) imaging revealed the progressive linearization of the collagen adjacent to the developing epithelial lesions (Fig 1E & F).
We next explored if collagen crosslinking could account for the dramatic ECM remodeling and stiffening. We noted an increase in the levels of the major reducible bifunctional collagen crosslinks, dehydrodihydroxylysinonorleucine (DHLNL) and hydroxylysinonorleucine (HLNL), in the breast tumors, reflecting elevated crosslinked collagen (Fig 1G). We further detected increased amounts of the amine oxidase crosslinking enzyme, LOX in the stromal cells of the premalignant Min foci and invasive tumors, and in the invading transformed epithelium (Fig 1H). These data establish an association between collagen crosslinking, LOX expression, ECM stiffness and tissue fibrosis in Neu-induced breast tumorigenesis.
We next asked if LOX-mediated collagen crosslinking could stiffen the breast and promote invasion of a premalignant lesion. We used Ha-ras human MCF10AT MECs which upon injection into mice develop into premalignant tissues (Hu et al., 2008). We conditioned inguinal mammary fat pads of NOD/SCID mice, surgically-cleared of their epithelium, with control fibroblasts or those expressing elevated LOX (Fig 2A; Supp Fig 2 & 3). Rheological measurement revealed that the mammary glands conditioned with LOX expressing fibroblasts were stiffer (Fig 2B), picrosirius red staining showed they had more fibrillar collagen (Fig 2C & D), and SHG imaging revealed they had more linearized collagen (Fig 2C & E). Consistent with ECM stiffening, resident fibroblasts in the epithelial-cleared LOX-treated glands showed more FAKpY397 and p130Cas immunostaining, indicative of increased focal adhesions and mechanosignaling in the stromal cells (Fig 2C; bottom).
LOX pre-conditioning and stiffening of the mammary gland promoted the growth and invasion of Ha-ras premalignant mammary organoids injected into these tissues as revealed by a significant increase in lesion size and tumors that lacked margins (Figs 2F, G & H). MECs in the LOX pre-conditioned glands also had more focal adhesions, as revealed by elevated FAKpY397 (Fig 2H) and p130Cas (not shown). To rule out any direct effect of LOX activity on MEC behavior, we also treated a cohort of animals in parallel (i.e. at time of MEC injection) with β–aminopropionitrile (BAPN), a natural and irreversible inhibitor of lysyl oxidase activity (Kagan and Li, 2003). Because BAPN treatment had no effect on tumor growth, invasion and focal adhesions (Supp Fig 4, 5, & 6) we concluded that it was LOX pre-conditioning of the stroma and gland stiffness that promoted mammary tumor progression, and not any direct effect of LOX on the mammary epithelium. These findings demonstrate how ECM crosslinking and stiffening can induce focal adhesions and promote the growth and invasion of an oncogene-initiated mammary epithelium in vivo.
We next asked if reducing LOX-dependent collagen crosslinking could temper tissue fibrosis and decrease focal adhesions, and whether this would inhibit breast tumor progression. We inhibited LOX activity using the cell soluble BAPN (Lucero and Kagan, 2006) or a LOX-specific function-blocking polyclonal which only inhibits extracellular LOX activity (Erler et al., 2006) and assayed collagen crosslinking, tissue fibrosis, focal adhesions and breast tumor development.
Inhibition of LOX activity was initiated in five month old parous animals, when LOX levels were already increased in the stromal cells but were non-detectable in the mammary epithelium (Fig 1H). Treatment was continued for one month after which the animals were allowed to recover for another month and then sacrificed (Fig 3A). At time of sacrifice, the non-treated MMTV-Neu mice had high levels of active LOX in the serum whereas BAPN or LOX inhibitory polyclonal-treated animals had reduced levels (Fig 3B). Mice with reduced LOX activity showed significant decreases in LOX-mediated collagen crosslinks, both reducible (DHLNL and HLNL) and nonreducible (pyridinoline) (Fig 3C & D), and the collagen fibrils adjacent to the epithelial lesions were less linear (Fig 3E & F). Consistent with the possibility that inhibiting collagen crosslinking prevented tissue fibrosis, LOX inhibition reduced fibrillar collagen (Fig 3G & H) and had reduced focal adhesions, as indicated by negligible FAKpY397 (Fig 3I).
Inhibiting LOX activity also increased tumor latency (Fig 4A) and decreased tumor incidence (Fig 4B), despite ErbB2 activity (Fig 4C). Moreover, the palpable lesions formed in the LOX-inhibited animals were smaller (Fig 4D) and less proliferative (Fig 4E). LOX inhibited mammary glands also stained positively for cytokeratin 14 along the basal periphery of the ducts, implying retention of their myoepithelium (Fig 4H & I). H&E sections revealed that a significantly greater proportion of the lesions in the LOX-inhibited animals were hyperplastic or premalignant (hyperplastic alveolar nodules, HAN, or mammary intraepithelial neoplasia, MIN) and the tumors that did develop were mostly low grade as opposed to the high grade carcinomas typically observed in the untreated Neu mice (Fig 4G & F). These results show how inhibiting LOX activity reduces collagen crosslinking, tempers tissue fibrosis, decreases focal adhesions, and impedes tumor progression to reduce breast tumor incidence.
We next assessed the effect of non-specifically inducing collagen crosslinking and stiffening on MEC invasion in the absence of fibroblasts, immune cells and other stromal and systemic cellular and soluble factors (Fig 5A experimental schemata). We explored the effect of nonspecific collagen crosslinking and stiffening on tumor invasion by adding nonmetabolizable L-ribose to the media of nonmalignant, MCF10A acini embedded in a 3D soft collagen I/reconstituted basement membrane gel (Col/rBM gel).
To determine whether MEC invasion required oncogenic signaling we utilized MCF10As expressing an ErbB2 chimera (ErbB2.chim; called HER-2; the human homologue of Neu) consisting of the extracellular and transmembrane domains of low-affinity nerve growth factor receptor (p75NGFR), and the cytoplasmic kinase domain of ErbB2 linked to the synthetic ligand-binding domain from the FK506-binding protein (FKBP). In these MECs addition of the synthetic bivalent FKBP ligand, AP1510, drives homodimerization of ErbB2, activation of the kinase domain and initiation of ErbB2 signaling (Muthuswamy et al., 2001). Chimeric ErbB2 signaling drives proliferation and luminal filling but fails to induce MEC invasion in rBM (Fig 5E). To study effects of homo- (ErbB2/ErbB2) and heterodimer (ErbB1/ErbB2) formation we also engineered MECs in which the wild type ErbB2 could be overexpressed through addition of doxycycline (ErbB2.TetOn; Supp Fig 7 & 8).
In the absence of ErbB2 activity MECs in collagen/rBM gels assembled acini, as illustrated by basally-oriented β4 integrin and cell-cell localized beta catenin (Fig 5E). Glycation-mediated crosslinking stiffened the collagen (Fig 5B), increased colony size (Fig 5C), and disrupted tissue organization, as revealed by diffusely localized beta catenin and the appearance of random cells within the lumens (Fig 5E). MECs within the ribose crosslinked collagen gels also had elevated levels and co-localized β1 integrin and FAKpY397, indicative of tension-induced focal adhesions (Fig 5D). Nevertheless, in the absence of ErbB2 activity, ECM stiffening did not drive MEC invasion (Fig 5E & F).
Addition of either AP1510 (1μM) or doxycycline (0.2μg/mL) to the mammary acini, induced and activated (ErbB2.TetOn) or directly activated ErbB2 (ErbB2.chim) (Supp Fig 9), promoted cell growth (not shown), drove luminal filling, and destabilized cell-cell junctions, as revealed by diffusely localized beta catenin (Fig 5E). Sustained ErbB2 activation did not drive MEC invasion, as indicated by colony integrity and the retention of basally-localized β4 integrin (Muthuswamy et al., 2001); Fig 5E & F). Yet, when ErbB2 was activated in colonies in the crosslinked, stiffened gels, colony architecture disintegrated, as revealed by the absence of detectable beta catenin and disorganized β4 integrin staining, and MECs invaded into the gels (Fig 5E & F). SHG imaging revealed that ErbB2 activation and ECM stiffening was accompanied by the appearance of prominent collagen bundles surrounding the colonies, and showed that single MECs invaded on fibrils that extended perpendicularly into the crosslinked, stiffened gels following ErbB2 activation (Fig 5E; Supp Fig 9). These findings show how collagen crosslinking and ECM stiffening, per se, cooperate with oncogenes such as ErbB2 to promote the invasive behavior of a mammary epithelium.
Interestingly, confocal imaging revealed elevated p130Cas and FAKpY397 staining that co-localized with β1 integrin (colocalization analysis of FAKpY397 and β1 integrin; Pearson's r = 0.78; p130Cas and β1 integrin, Pearson's r = 0.89) in the stiffer breast tissue of the Neu mice (Fig 6A; see insert) and reduced levels of FAKpY397 following LOX inhibition (Fig 3H). Moreover, inhibiting β1 integrin activity, using the function blocking antibody AIIB2, or reducing integrin signaling by expressing an inducible FRNK (FRNK.TetOn; Supp Fig 10) prevented the force-mediated invasion of the ErbB2 activated mammary organoids (Fig 5G & H). These findings show how ECM crosslinking and stiffness cooperate with an oncogene to promote breast cell invasion and implicate integrin signaling in force-dependent tumor progression.
To determine if integrin signaling would be sufficient to induce breast tumor invasion we expressed a series of integrin constructs in nonmalignant MCF10A and Ha-ras premalignant MCF10AT MECs and assayed for invasive behavior in rBM and in vivo (Fig 6B).
Expression of the V737N integrin, which recapitulates tension-dependent integrin clustering, promoted focal adhesions, indicated by elevated FAKpY397 (Fig 6C) and disrupted the integrity of mammary colonies in rBM, revealed by luminal filling and altered β4 integrin localization (Fig 6C; top). In contrast, neither expression of a wild type (Fig 6C) nor a constitutively active β1 integrin (not shown; (Paszek et al., 2005)) induced focal adhesions and disrupted mammary tissue architecture. Moreover, while the V737N β1 integrin mutant failed to promote invasion of the MCF10A MECs (Fig 6C), the V737N integrin induced the invasion of the Ha-ras premalignant MCF10AT colonies in rBM (Fig 6D & E). Upon injection into nude mice the V737N integrin not only promoted focal adhesions, and increased lesion size (Fig 6F), but also induced the invasive behavior of the Ha-ras MCF10AT organoids, as revealed by the loss of epithelial lesion margins and increased FAKpY397(see arrows in Fig 6G). These findings implicate tension-dependent integrin clustering and focal adhesions in breast tumor invasion. However, because integrin clustering could only promote invasion in Ha-ras premalignant MECs, they also illustrate how integrin-mediated mechanotransduction cooperates with oncogenic signaling to drive malignancy.
Integrins active PI3K, and PI3K promotes invasion in culture and tumor progression in vivo (Webster et al., 1998). Therefore, we explored the relationship between focal adhesions and PI3K signaling in tension-dependent breast tumor invasion. We found Akt signaling, an established target of PI3K, to be elevated in the premalignant and malignant, rigid mammary tissue (Fig 7A) and in the mammary colonies in the ribose-stiffened collagen gels (Fig 7B).
We examined the effect of ECM rigidity on PI3K activity in MECs plated on rBM-functionalized polyacrylamide gels (rBM PA gel) with elastic moduli of 140-400 (soft) and ≥5000-10,000 (stiff) Pascals. These two extremes represent the ECM stiffness of healthy versus transformed breast tissue. Although substrate stiffness did not increase the levels of AktpS473 in unstimulated MECs, ECM stiffness potentiated the magnitude of EGF-activated AktpS473 (Fig 7C) and increased ErbB2-activated AktpS473 (Fig 7D). MECs on soft gels that expressed the β1 integrin cluster mutant, but not the wild-type β1 integrin, also showed a significant increase in AktpS473 activity following EGF stimulation. These results suggest integrin mechanotransduction potentiates growth factor dependent PI3 kinase signaling (Fig 7E; Fig 6B & C).
Pharmacological inhibition of PI3K activity with LY294002 restored the colony architecture of ErbB2-activated MECs in ribose crosslinked collagen gels towards that of a non-invasive, polarized, cohesive colony (Fig 7F & G). Inhibiting PI3K activity reduced colony size, and immunostaining revealed that colonies treated with LY294002 retained β catenin at cell-cell junctions and had basally-localized β4 integrin (Fig 7F). The epithelium from the LOX-inhibited Neu mice also had lower PI3K signaling, as revealed by fainter active Akt/PI3K Substrate staining (Fig 7H). These data are consistent with a role for integrin mechanotransduction in PI3K-mediated breast tumor invasion. The findings suggest that ECM stiffness, as induced by elevated collagen crosslinking could promote breast malignancy by enhancing integrin-GFR crosstalk (Fig 7I; (Miranti and Brugge, 2002)).
Our findings identify collagen crosslinking as a critical regulator of desmoplasia and imply that the level and nature of ECM crosslinks in a tissue could impact cancer risk and alter tumor behavior. The observations are consistent with links between ECM crosslinking and tissue stiffening in tissue fibrosis and could explain the increased risk to malignancy associated with these conditions (Colpaert et al., 2003). They might also explain why women with mammographically dense breasts have an increased relative risk of developing cancer (Martin and Boyd, 2008). Because aged tissues are stiffer and contain high levels of aberrant collagen crosslinks, the data offer a new paradigm for understanding why tumor incidence increases so dramatically with aging (Szauter et al., 2005).
Tissue fibrosis influences tumor progression by regulating soluble factors that induce inflammation and angiogenesis and stimulate cell growth and invasion (Bierie et al., 2009; Coussens et al., 1999). We showed that modifying the state of collagen crosslinking and ECM stiffness, two physical parameters of the tissue microenvironment, modulated the invasive behavior of an oncogene pre transformed mammary epithelium, even in the absence of cellular and soluble tissue and systemic factors. The findings imply that tissue fibrosis could regulate cancer behavior by influencing the biophysical properties of the microenvironment to alter force at the cell and/or tissue level. Importantly, we noted that focal adhesions were elevated in the stiffened breast tumors and organoid cultures, that forcing focal adhesions promoted MEC invasion and that inhibiting focal adhesion signaling or tempering tissue stiffening reduced focal adhesions and tumor invasion. These observations are consistent with the notion that force regulates the invasive behavior of tumors by modulating integrin activity and focal adhesion assembly and signaling (Paszek et al., 2005). The findings thereby provide an explanation for why pYFAK and p130Cas are so often increased in breast tumors (Cabodi et al., 2006; Madan et al., 2006), even when integrin expression is frequently decreased (Koukoulis et al., 1993; Zutter et al., 1998). Indeed, the observations suggest that enhanced integrin signaling rather than just an increase in integrin expression is more critical for tumor progression.
Our data show how modulating the activity of one class of ECM crosslinking enzymes, the LOXs, can directly modify tumor progression by regulating collagen crosslinking and stiffness. The results are consistent with data indicating that LOX enzymes are elevated in many cancers (Erler and Weaver, 2009) and that LOX is induced by hypoxia inducible factor (HIF-1) and TGFβ; two key regulators of tumor behavior (Postovit et al., 2008). Indeed, cellular LOX promotes breast cell migration and invasion and enhances tumor proliferation and survival (Kirschmann et al., 2002). Hypoxia-induced LOX modulates tumor metastasis by regulating integrin function (Erler and Giaccia, 2006), by facilitating tumor extravasation (Bondareva et al., 2009) or by conditioning the metastatic niche (Erler et al., 2009). Our work indicates that LOX can promote tumor progression and MEC invasion by increasing fibrillar collagen and ECM stiffness. These observations are consistent with the major function of LOX in tissues as a key enzyme for collagen and elastin crosslinking that enhances tensile strength (Szauter et al., 2005). Consistently, by inhibiting LOX activity early, when levels were high in the stroma we prevented ECM remodeling and stiffening and reduced tumor progression in the MMTV-Neu mice. Because a LOX-specific inhibitory polyclonal that cannot inhibit intracellular LOX also prevented fibrosis and tumor progression our results suggest that LOX-mediated collagen crosslinking likely regulates breast tumor progression by modifying the tumor microenvironment rather than by directly changing cell behavior.
We observed that LOX inhibition reduced focal adhesions and PI3K signaling indicating that LOX modulates breast tumor progression by stiffening the ECM to drive focal adhesions assembly and enhance GFR-dependent PI3K signaling. Consistently, we showed that ribose-mediated collagen crosslinking, which induces nonspecific collagen glycation, also stiffened the ECM and enhanced focal adhesions and PI3K signaling to promote ErbB2-dependent breast tumor invasion. We noted that MEC invasion could be abrogated by inhibiting integrin and FAK activity, thereby illustrating the importance of ECM crosslinking and stiffness in tumor progression. This idea is consistent with our recent findings that LOX conditioning of the lung ECM promotes breast tumor metastasis (Erler et al., 2009), and data showing that fibrotic breast tumors have the poorest prognosis and highest rate of recurrence (Hasebe et al., 1997). Indeed, our findings underscore the notion that ECM crosslinking and stiffness, per se, is a key regulator of tumor progression. They imply that other ECM crosslinkers/modulators implicated in tissue fibrosis such as tissue transglutaminase, lysyl hydroxylase or some of the proteoglycans or even non-specific metabolic glycation end products (AGEs) might also similarly promote malignancy.
LOX has been proposed to be a tumor suppressor (Payne et al., 2007) possibly by directly inhibiting ECM adhesions and integrin signaling (Zhao et al., 2008). LOX-mediated ECM stiffening could also impede cell invasion in the absence of MMP activity (Zaman et al., 2006) reminiscent of highly crosslinked, stiff fibrotic tissues and scars that often never progress to malignancy. We noted that neither ECM stiffness nor forced integrin clustering induced mammary tissue invasion in the absence of oncogenic signaling. This suggests that other factors that modulate integrins and/or ECM remodeling or cellular tension likely cooperate with ECM crosslinking and force to promote tumor invasion (Katz et al., 2007; Wolf et al., 2007). Instead, ECM stiffness appears to operate as a signaling rheostat potentiating oncogenic cues to promote tumor invasion.
Cancer progression is accompanied by MMP-dependent ECM remodeling. Multiple MMPs are over expressed in the tumor stroma, and some MMPs are up regulated in transformed epithelia (Jodele et al., 2006; Page-McCaw et al., 2007). Elevated expression of specific MMPs induced desmoplasia and malignant transformation (Sternlicht et al., 1999) and genetic ablation of MMPs or pharmaceutical inhibition of MMP activity reduced breast metastasis (Martin et al., 2008). These data argue that MMPs are critical for malignancy. Nevertheless, clinical trials with MMPs failed, suggesting the role of MMPs in cancer is more complicated (Coussens et al., 2002). Indeed, MMPs collaborate with crosslinking enzymes such as LOX to facilitate collagen maturation, and MMPs and LOX regulate the expression and activity of soluble factors such as transforming growth factor beta that regulate tumor cell behavior (TGFβ), (Atsawasuwan et al., 2008; Csiszar, 2001; Decitre et al., 1998; Szauter et al., 2005). TGFβ in turn regulates the expression of many ECM proteins and modifying enzymes including LOXs, and TGFβ increases levels of factors that evoke inflammation, induce fibrosis and promote metastasis (Bierie and Moses, 2006; Oleggini et al., 2007). Indeed, force itself modulates TGFβ activation and compression alters growth factor signaling (Tschumperlin et al., 2004; Wipff et al., 2007). These findings underscore the dynamic and reciprocal relationship between ECM deposition, processing and degradation. Thus, cancer is best viewed as a dynamic, phenotypically-plastic and highly coordinated tissue remodeling process that is tightly regulated by biochemical and mechanical cues. Accordingly, not only will we need to clarify the role of ECM cleavage in tumors but we will also be obliged to understand how ECM remodeling is integrated within the context of its deposition, post translational modifications and topological rearrangement and to take into consideration the effect of mechanical force as a key regulator of malignancy.
Antibodies were: β4 integrin (3E1); β1 integrin (AIIB2; Chemicon); FAK (77), YES (1), β1 integrin (18), E-Cadherin (610405; BD Transduction); laminin-5 (BM165; MP Marinkovich); β actin (AC-15; Sigma); ErbB2 (3B5; Calbiochem); polyclonal β catenin (Sigma); FAKpY397 (BioSource); Phospho-(Ser/Thr) Akt Substrates and AktpS473(Cell Signalling); Akt (BD Pharmingen); p130Cas, ErbB2pY1248 (Abcam); cytokeratin 14 (Covance); LOX (A. Giaccia, Stanford University); LOX polyclonal activity inhibitory antibody (OpenBiosystems); and secondary AlexaFluor goat anti-mouse, anti-rabbit, and anti-rat (488- and 555 conjugates), AlexaFluor phalloidin (488-conjugate, Invitrogen); Donkey anti-mouse and anti-rabbit (Cy2- and Cy3-conjugates; Jackson ImmunoResearch); and Sheep anti-mouse and anti-rabbit HRP-linked (Amersham). Reagents included: LY294002; (50μm in DMSO; Calbiochem).
MEC and fibroblast cell lines were cultured as described (Paszek et al., 2005). Collagen crosslinking was induced by addition of 15mM L-ribose to the culture medium (Girton et al., 1999). rBM-conjugated PA gels with calibrated stiffness were prepared as described (Johnson et al., 2007).
Full length human ErbB2 (K. Ignatoski) was cloned into the pRet puro Tet IRES EGFP tetracycline-inducible vector. The β1 integrin wild type, β1 integrin glycan wedge constitutively active and β1 integrin clustering mutant V737N constructs and the preparation of virus and cell infection and selection have been described (Paszek et al., 2005). Four myc-tags were added to the C-terminus of full length LOX and cloned into the pLV puro TetO7mCMV tetracycline-inducible lentiviral vector and expressed biscistronically with EGFP.
Mammary glands and gels were assayed for materials properties by unconfined compression and rheometrical analysis (Paszek et al., 2005).
FVB-TgN MMTV-Neu, NOD/SCID, and BalbC nu/nu mice (Jackson Laboratory) were maintained in accordance with University of Pennsylvania and University of California IACUC guidelines. For LOX inhibition studies animals were treated with BAPN (3mg/kg; Spectrum) in the drinking water (4-8 mice/group; 4 studies) or a LOX function-blocking polyclonal (3mg/kg; OpenBiosystems, D8746) injected intraperitoneally twice per week (3-4 mice/; 1 study). Mice were sacrificed at 7-71/2 months of age at which time tail vein blood was collected. Lesions were detected by palpation (~3mm diameter) and tumor volume was assessed using calipers. At sacrifice mammary glands were excised, imaged and mechanically tested or snap frozen or paraformaldehyde fixed.
Tumor grading was performed blinded on H&E stained sections from untreated (n=14) or BAPN treated (n=13) #2-3 mammary glands. Premalignant lesions were defined as hyperplastic alveolar hyperplasia (HAN) or Mammary Intraepithelial Neoplasia (MIN)-like foci. Grade I lesion were well defined as homogenous carcinomas, Grade II contained areas with strong necrosis, stromal reaction and/or red blood cells outside of tumor blood vessels and Grade III also contained necrosis and nuclear pleiomorphy. Adjacent tissue was defined as mammary tissue surrounding a tumor that was cut away from the tumor prior to subsequent analysis. A small set of anti-LOX treated mice (n=4) was compared with their controls (n=3), and showed the same tendency to less progressed lesions as was observed in the BAPN treated animals.
NOD/SCID mice (n=24) were used for mammary fat pad transplantation studies (Kuperwasser et al., 2004). Briefly, the rudimentary inguinal epithelium was removed from three week old anesthetized female mice and 5 × 105 NIH 3T3 WT or LOX-expressing fibroblasts (2.5 × 105 were treated with 4Gy irradiation 24 hours prior to injection) were injected into the left and right mammary glands. Two weeks following fibroblast injection, 1×106 DCIS.com MCF10AT MEC 4 day old rBM-generated, proliferating organoids (16-20 cells/organoid) were suspended in Dulbeccos modified PBS and injected into the pre-conditioned fat pads. All mice were sacrificed at 8 weeks of age (3 weeks following MEC injection and 5 weeks after fibroblast injection), lesion volume was assessed by caliper measurement, photographed In Situ, and dissected gland fragments were imaged and mechanically-tested or snap frozen, or fixed and paraffin embedded.
Proliferating rBM-generated organoids (16-20 cells/organoid) from each experimental condition were injected subcutaneously into the rear flanks of BalbC Nu/Nu mice (6-8 mice/group; 5-10×106) and tumor formation was monitored for three weeks and samples were assessed as above at study termination.
Mammary gland collagen was reduced with standardized NaB3H4, hydrolyzed with 6N HCl and subjected to amino acid and collagen crosslink analyses as described (Yamauchi and Shiiba, 2008). The reducible crosslinks, dehydro-dihydroxylysinonorleucine (deH-DHLNL) and deH-hydroxylysinonorleucine (deH-HLNL), their ketoamines, were identified as their reduced forms, i.e. DHLNL and HLNL. The crosslinks analyzed (reducible and nonreducible) were quantified as moles/mole of collagen based on the hydroxyproline value of 300 residues per collagen molecule. LOX activity was measured in cell supernatant and plasma as described (Erler et al., 2006).
Immunofluorescence and imaging of 3D cultures and tissues was as described (Paszek et al., 2005). Picrosirius red analysis was achieved using paraffin sections of mammary glands stained with 0.1% Picrosirius Red (Direct Red 80; Sigma) and counterstained with Weigert's Hematoxylin to reveal fibrillar collagen. Sections were serially imaged using an Olympus IX81 fluorescence microscope fitted with an analyzer (U-ANT) and polarizer (U-POT; Olympus) oriented parallel and orthogonal to each other and quantified using minimal thresholding. Two-photon second harmonics imaging was performed on a Prairie Technology Ultima System attached to an Olympus BX-51 with a water immersion objective and samples were quantified by calculating the linearity of multiple collagen fibrils (see Appendix for further details).
Cells were lysed in RIPA or Laemmli buffer and assayed by immunoblotting (Johnson et al., 2007).
Statistical analysis was performed with GraphPad Prism using an unpaired student's t-test, two-way ANOVA, or Fisher's exact test.
We thank K. Ignatoski for the ErbB2 construct, MP Marinkovich for the BM165 antibody, P. Mrass for 2 photon microscopy guidance and R.G. Wells for mentoring of KRL. The work was supported by NIH grants R01-CA078731 to VMW, R01-CA057621 to Z. Werb, and T32HL00795404 to KRL, and grants DOD W81XWH-05-1-330, DOE A107165 and CIRM RS1-00449 to VMW.
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