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Renal cell carcinomas (RCC) frequently express the gastrin-releasing peptide receptor (GRP-R). Gastrin-releasing peptide (GRP) stimulates tumor cell proliferation and neoangiogenesis. Tumor-associated macrophages (TAM) comprise an important cellular component of these tumors. We analyzed the GRP/GRP-R network in clear cell RCC (ccRCC) and non-clear cell RCC (non-ccRCC) with special regard to its expression by macrophages, tumor cells and microvessels.
Gastrin-releasing peptide and GRP-R expression in 17 ccRCC and 9 non-ccRCC were analyzed by RT-PCR, immunohistochemistry and double immunofluorescence staining.
Tumor-associated macrophages expressed GRP and GRP receptor in ccRCC. Tumor cells and microvessels showed low to intermediate GRP-R expression in nearly all cases. In 12 ccRCC tumor epithelia also expressed low levels of GRP. Microvascular GRP expression was found in nine cases of ccRCC. For non-RCC, the expression of GRP and GRP receptor expression pattern was similar.
Tumor-associated macrophages are the main source of GRP in RCC. GRP receptor on TAM, tumor epithelia and microvessels might be a molecular base of a GRP/GRP receptor network, potentially acting as a paracrine/autocrine modulator of TAM recruitment, tumor growth and neoangiogenesis.
Gastrin-releasing peptide (GRP) is the human analog of the amphibian tetradecapeptide bombesin. McDonald et al.  was the first to describe GRP in the gastrointestinal tract of mammals. GRP, originally named for its ability to stimulate the release of gastrin, modulates the secretion of a variety of gastrointestinal hormones and affects pancreatic secretion, intestinal transit, muscle contractility, metabolism and behavior . The expression of GRP is not only restricted to the gastrointestinal tract and it is also widely distributed in the central nervous system.
GRP interacts with four different G-protein coupled receptors: the GRP receptor (subtype I), the neuromedin-B receptor, the Bombesin receptor (subtype 3), and a novel subtype 4 that has been identified in frogs. In humans, GRP binds to the GRP receptor with high affinity and to the subtype 3 receptor with low affinity.
GRP has been identified as an important growth factor not only for neuroendocrine malignancies, such as medullary thyroid carcinomas , small cell lung carcinomas  and neuroblastomas , but also for carcinomas of the breast , colon , prostate  and rat pancreatic cancer . The growth of renal cell carcinoma (RCC) has been linked to the presence of GRP and its receptor by Pansky et al.  who stimulated the growth of various RCC cell lines with GRP. Reubi et al.  identified the GRP receptor on tumor epithelia in human RCC specimens using a radioactive ligand. We have shown recently that the GRP receptor is not only found on tumor epithelia, but also expressed in microvessels . We likewise demonstrated that the microvascular GRP receptor is potentially relevant for neoangiogenesis in RCC, because microvessel formation is inhibited by the GRP receptor antagonist RC-3095 in an animal model of a dorsal skinfold chamber.
Malignant tumors comprise up to 50% stromal cells of which monocytes/macrophages are a quantitative and functional important subpopulation. The tumor microenvironment and hypoxia induce a differentiation of tumor-associated macrophages (TAM) into a phenotype with depressed cytotoxicity [13–15] which may enhance growth and spread of tumor cells [16–18].
Neuropeptides, e.g. GRP, significantly modulate the function of macrophages. The GRP receptor has been found on macrophages, and GRP has an effect on macrophage function such as displayed by an alteration of adhesion, migration and phagocytosis [19, 20]. Interestingly, GRP expression in macrophages has been reported only under inflammatory conditions, such as chronic bronchitis and lung inflammation and fibrosis [21, 22]. In inflammation, the findings of simultaneous peptide and receptor expression suggest an autocrine loop in the macrophage environment that may be important for the macrophage/epithelium interaction.
In the present study, we confirm the presence of GRP and GRP receptor mRNA transcripts in tumor tissue of human clear cell RCC (ccRCC) and non-clear cell RCC (non-ccRCC). Moreover, as novel finding, we co-localize an expression of GRP and GRP-R in TAM and also in microvessels. We conclude that the GRP/GRP receptor system in RCC and TAM may represent a link between growth regulation in the tumor and local immune response.
Seventeen ccRCC and nine non-ccRCC were freshly obtained at the time of surgery from the urological department of our institution. Approval of the ethics committee had been obtained before initiation of the study. Histopathological data are summarized in Table 1.
Tissues were fixed in HOPE™ (Hepes–glutamic acid buffer-mediated organic solvent protection effect) solution (DCS Diagnostic Systems, Hamburg, Germany) and embedded in paraffin according to the manufacturer’s instructions. Tissue sections (3 μm) were mounted on glass slides, de-paraffinized, rehydrated and subjected to immunohistochemistry. Sections were incubated with a polyclonal rabbit anti-gastrin-releasing peptide antibody (1:50 dilution, Dako, Hamburg Germany) or polyclonal rabbit anti-gastrin-releasing peptide receptor (GRP-R) antibody (1:200 dilution; kindly donated by Dr. Battey, NIDCD, Rockville, MD) at room temperature for 2 h. After several washing steps, the sections were subsequently incubated with Envision™ peroxidase (Dako) for 30 min. Signals were detected with diaminobenzidine as substrate (Dako). Finally, sections were counterstained with hematoxylin, dehydrated with ethanol and xylene and covered with cover slips.
Immunohistochemical staining for GRP and its receptor was semiquantitatively analyzed by means of an immunoreaction score: 0, no staining; 1 staining <10% of cells; 2 10–50% of cells stained; 3 >50% of cells stained.
For double immunofluorescence analysis, sections were incubated with a mixture of anti-GRP (1:25) and CD68 (1:3,000, Dako Clone KP-1) at 4°C overnight. Anti-CD 68 antibody was detected with an anti-mouse Cy3 conjugate (1:500 dilution for 1 h at RT). Subsequently, the sections were incubated with anti-rabbit Envision-Peroxidase (Dako) for 1 h at RT and incubated with tyramide-FITC to detect GRP (tyramid signal amplification, PerkinElmer/NEN, Rodgau, Germany). Finally, sections were mounted with fluoromount (Dako). Immunofluorescence stainings were visualized by means of an Axiophot fluorescence microscope (Zeiss, Göttingen, Germany) and a fluorescence camera (Fview, Olympus, Hamburg, Germany).
Paraffin sections of HOPE-fixed tissue were cut under RNAse-free conditions and transferred to reaction tubes. The sections were de-paraffinized with three changes of isopropanol at 60°C for at least 90 min. The sections were washed with absolute ethanol, air dried and lysed in lysis buffer applying the RNAeasy mini kit (Qiagen, Hilden, Germany), and RNA was extracted according to the manufacturer’s instructions. The quality and quantity of isolated RNA were tested in an automated capillary electrophoresis system (Agilent BioAnalyzer 2100; Agilent Technologies, Waldbronn, Germany). A maximum of 500 ng of total RNA was reverse transcribed using random hexamer primers (Invitrogen, Karlsruhe, Germany) and Omniscript™ reverse transcriptase (Qiagen) in a 20 μl volume (25 ng RNA/μl) at 37°C for 60 min according to the manufacturer′s instructions.
A 25 ng of cDNA was subjected to PCR analysis in a total volume of 20 μl using Hotstart Mastermix (Qiagen) and primer pairs with conditions as summarized in Table 2. Porphobilinogen deaminase was used as a house-keeping gene which is constantly expressed in renal carcinomas. PCR products were separated on a 1.5% agarose gel, stained with ethidium bromide and analyzed on a UV transilluminator. The used primers are given in Table 2.
For the analysis of the immunohistological staining, the one-way ANOVA with Dunnett’s post test was performed using GraphPad Prism version 4.00 for Windows, GraphPad Software, San Diego CA USA, http://www.graphpad.com.
mRNA expression analysis of GRP and GRP receptor was performed in serial sections of the same tissue blocks used for immunohistochemistry. Particularly for GRP, we could demonstrate that GRP is synthesised within the tumor environment of ccRCC and non-ccRCC (Fig. 1; Table 1).
In ccRCC tumor cells with a low GRP signal were observed in 12 cases. The mean GRP scores in tumor cells (scoremean 0.71) and tumor vessels (scoremean 0.59) were significantly lower than in TAM (scoremean 1.65) (P < 0.01). Therefore, TAM were the main source of GRP in ccRCC.
Addressing the question which cell types express GRP receptor, a low to high signal intensity was detected in ccRCC. The mean GRP receptor expression was significantly lower in tumor epithelia (scoremean 1.35) than in TAM (scoremean 1.94) (P < 0.0.5) and lower in association with tumor microvessels (scoremean 1.58).
In non-ccRCC, a low GRP signal of tumor cells was detected in three cases and an intermediate signal in two cases. The mean GRP scores in non-ccRCC tumor cells (scoremean 0.78) and tumor vessels (scoremean 0.44) were significantly lower than in TAM (scoremean 2.11) (P < 0.05). For GRP-R expression, non-ccRCC exhibited the same pattern as ccRCC, but no significant difference was detected (data not shown).
When comparing immunohistochemically stained serial sections, we also found GRP and GRP receptor-positive macrophages and GRP receptor-positive tumor cells located in close vicinity (Fig. 2).
To confirm this, we performed double immunofluorescence staining with CD 68 and GRP antibodies macrophages within RCC expressed both proteins on their surface as demonstrated by the orange composite signaling in confocal microscopy (Fig. 2).
Comparative analyses of the degree of differentiation, and the tumor stage did not reveal any correlation. The data on all patients are summarized in Table 1.
Analysis of tumor-free tissues of nine cases revealed a strong GRP and GRP-R expression in tubules and collecting ducts in contrast to peritubular capillaries where no expression could be found. No GRP or GRP receptor-positive macrophages were found in tumor-free tissue.
The present study provides evidence that GRP and its high-affinity receptor are simultaneously expressed in renal carcinomas. The staining pattern of tumor cells and microvascular endothelia confirmed our previous results on the GRP receptor expression in 18 ccRCC . In the present study, we used HOPE fixation, which allowed the simultaneous detection of specific mRNA transcripts and of proteins by means of RT-PCR and immunohistochemistry in 17 ccRCC and 9 non-ccRCC.
In most cases, we found a co-expression of mRNA and protein. Only in cases with RNA degradation and hypoxic necrosis differences between mRNA and protein expression were observed. Protein expression was located nearby or within the necrotic rims. The absence of mRNA expression for GRP can be explained by an advanced degradation of mRNA, even in cases with detectable PBGD mRNA which is abundantly expressed in renal carcinomas.
Immunohistochemical analysis of the GRP receptor expression has been described previously. Detection of the ligand using a polyclonal GRP antiserum has also been reported [23, 24]. We found cytoplasmatic signals for GRP, particularly in TAM and in lower intensity in tumor epithelia. Endothelial expression was found at low levels in few cases, predominately in ccRCC. GRP receptor expression analysis was positive, particularly in TAM and microvessels and with lower intensity in tumor cells of all cases. The discontinuous and granular staining for the GRP receptor was in contrast to the study of Scott et al.  who found a more homogeneous cytoplasmatic staining for the GRP receptor in carcinoid tumor epithelia, whereas the staining pattern for GRP corresponded well to our data. GRP and GRP expression has been analyzed in a broad number of neoplasias.
Up til now, investigators did not pay attention on the expression of GRP and GRP-R on macrophages and microvessels. The expression of bombesin/GRP in immune cells has been identified in circulating peripheral monocytes and in alveolar macrophages . Furthermore, GRP acts as chemoattractant for murine peritoneal macrophages  and potentially stimulates cytotoxic natural killer cells both in vivo and in vitro . In contrast, Meloni et al.  showed that bombesin/GRP stimulates the release of interleukin-8 (IL-8) by peripheral monocytes and may thereby promote neoangiogenesis and tumor growth indirectly. In renal carcinomas, a high number of infiltrating monocytes and macrophages have already been identified . The stimulation of the GRP-R induced the release of interleukin-8 and vascular endothelial growth factor in human prostate cancer cell lines .
The detection of the GRP-R on tumor microvessels underlines the importance of GRP for the progression of renal carcinomas and suggests the presence of an autocrine or paracrine loop within the tumor. We have shown previously that the density of perfused microvessels and tumor blood flow are reduced if a specific GRP receptor antagonist is administered into nude mice bearing subcutaneously implanted renal carcinomas . However, our finding has been questioned by Busby et al.  who demonstrated that bombesin/GRP did not have any mitogenic effect on isolated human vascular endothelial cells (HUVEC). This discrepancy may be explained by the fact that HUVEC originate from the umbilical cord and the findings that we have also identified GRP receptors on tumor pericytes that may also be involved in the proliferation of endothelia.
In conclusion, our study confirms the presence of both GRP and GRP receptor in ccRCC. TAM are the main source of intratumoral GRP. The results suggest a paracrine/autocrine signaling within renal carcinomas between TAM, tumor epithelia and microvessels; whereas, the functional relevance of GRP receptors in microvessels and tumor epithelia has been investigated, the significance and the function of the GRP receptor expression in macrophages needs further elucidation.
Open Access This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
J. Bedke and B. Hemmerlein contributed equally to this work.