Hedgehog pathway activity in the LADY prostate tumor model
© Gipp et al; licensee BioMed Central Ltd. 2007
Received: 10 January 2007
Accepted: 07 March 2007
Published: 07 March 2007
Robust Hedgehog (Hh) signaling has been implicated as a common feature of human prostate cancer and an important stimulus of tumor growth. The role of Hh signaling has been studied in several xenograft tumor models, however, the role of Hh in tumor development in a transgenic prostate cancer model has never been examined.
We analyzed expression of Hh pathway components and conserved Hh target genes along with progenitor cell markers and selected markers of epithelial differentiation during tumor development in the LADY transgenic mouse model. Tumor development was associated with a selective increase in Ihh expression. In contrast Shh expression was decreased. Expression of the Hh target Patched (Ptc) was significantly decreased while Gli1 expression was not significantly altered. A survey of other relevant genes revealed significant increases in expression of Notch-1 and Nestin together with decreased expression of HNF3a/FoxA1, NPDC-1 and probasin.
Our study shows no evidence for a generalized increase in Hh signaling during tumor development in the LADY mouse. It does reveal a selective increase in Ihh expression that is associated with increased expression of progenitor cell markers and decreased expression of terminal differentiation markers. These data suggest that Ihh expression may be a feature of a progenitor cell population that is involved in tumor development.
Sonic hedgehog (Shh) is one of three mammalian hedgehog (Hh) genes [Sonic hedgehog, Desert hedgehog, Indian hedgehog]. Each of the Hh genes encodes a secreted signaling peptide that binds to a membrane bound receptor (Ptc). Binding of Hh ligand to the Ptc receptor on the target cell initiates an intracellular signal transduction cascade that ultimately activates expression of Hh target genes through the activity of a family of Gli transcription factors . Previous studies have identified Shh as an important regulator of prostate development [2–7]. Shh is expressed exclusively in the epithelium of the developing prostate. Expression is most abundant during prostate ductal budding and postnatal ductal morphogenesis and diminishes to a low level in the adult. Ihh is also expressed in the prostate epithelium. It is expressed at relatively lower levels in the developing prostate but in a distinctive pattern and, in contrast to Shh, its expression is maintained undiminished in the adult . Shh expressed by the Urogenital Sinus (UGS) epithelium induces mesenchymal Hh target gene expression indicating a paracrine mechanism of action [2–5, 7]. Paracrine signaling directly affects mesenchymal proliferation [3, 7], but also influence epithelial proliferation and differentiation by paracrine feedback mechanisms [[4, 7, 9], manuscript in preparation]. Autocrine or juxtacrine signaling is a prominent feature of Hh actions in development  and several lines of evidence now suggest that autocrine signaling stimulates prostate epithelial proliferation [6, 10].
Recently Hh signaling has been identified as an important factor in prostate cancer. Paracrine signaling from tumor cells has been shown to activate Hh target gene expression in the adjacent stroma and xenograft studies indicate that paracrine signaling can accelerate tumor growth . In addition, evidence has been presented suggesting that autocrine signaling may also occur, particularly in advanced prostate cancer, and directly drive tumor cell proliferation [11–13]. These studies have generated considerable interest in understanding the role of Hh signaling in prostatic neoplasia. We report here the first characterization of Hh signaling in a transgenic mouse model of prostate cancer.
The LADY tumor is a transgenic mouse model of prostate cancer in which the large T antigen gene containing the deletion mutation d1 2005 (removing expression of small t antigen) is driven from the prostate specific probasin promoter . As compared to the TRAMP mouse model, tumors in LADY transgenic mice (Line 12T-7f) develop and progress through epithelial hyperplasia, reactive stromal hyperplasia, dysplasia and mouse intraepithelial neoplasia (mPIN) similar to that observed in human high grade PIN. Transgene expression is under androgen control since the probasin promoter is developmentally regulated by androgens . Thus, changes in epithelial cell architecture occur in all prostatic lobes as early as four weeks of age and are identified as clusters of cells containing elongated, hyperchromatic nuclei interspersed among normal epithelial cells. Reactive stromal proliferation occurs in parallel with epithelial cell transformation. These changes are complete by seven to eight weeks and the resulting tumors progress from lesions resembling human low-grade PIN with epithelial stratification and mild nuclear atypia to HGPIN with marked nuclear atypia by 15 weeks of age. Although rapid tumor growth precludes maintaining these mice much beyond four months, micro-invasion and metastases are rarely seen.
Several groups have examined the expression of Hh ligands and Hh signaling activity in human prostate cancer with inconsistent findings. We first reported that robust Shh expression and Gli1 expression was characteristic of both the normal adult human prostate as well as benign prostatic hyperplasia and prostate cancer . Karhadkar  reported that Shh and Ihh were both expressed in localized prostate cancer and benign tissue but that the Hh target genes Ptc and Gli1 were expressed only in metastatic tumors. Sanchez et al  reported findings suggesting a basal level of Shh, Ptc and Gli1 expression in benign tissue that is variably increased in cancer while Sheng et al observed increased Ptc expression that was attributable in part to mutations that dysregulate Hh signal transduction. These studies have left unresolved the role of Hh signaling in tumor development and progression and for this reason an examination of the Hh pathway in transgenic tumor models may be instructive. The data reported here clearly shows that a net increase in Hh signaling, as measured by expression of the conserved Hh target genes Ptc and Gli1, is not a feature of tumor development in the LADY mouse.
An unexpected and provocative finding was that a net decrease in Hh pathway activity during tumor development, as measured by Ptc expression, actually embraced divergent changes in expression of the two Hh ligands. Shh expression was decreased while Ihh expression was dramatically increased. These changes were evident as early as three weeks of age (data not shown). Shh and Ihh are highly related ligands which show functional redundancy in their ability to activate the Hh signal transduction pathway, but Shh and Ihh are expressed in unique patterns during prostate development. Whereas Shh expression localizes to the tips of the developing ducts, Ihh expression localizes to the epithelium of the urethral lumen and the origin of the developing ducts. Shh is expressed abundantly during prostate development and gradually diminishes to a low level in the adult prostate . In contrast, lower level Ihh expression is maintained at a fairly constant level throughout development and in adulthood . We have observed two other circumstances where prostate Ihh expression is increased. The first is during prostate development in the Shh transgenic null, where Hh signaling is maintained by a significant increase in Ihh expression . The second is during castration-induced involution of the VP, where there is a marked increase in Ihh expression without a comparable increase in Shh expression (unpublished observations). Taken together, these findings suggest that Shh and Ihh are differentially regulated and, while exhibiting some degree of functionally redundancy, may normally play different roles in prostate growth regulation. Indeed, studies of Hh signaling in prostate development suggest that Hh signaling exerts a variety of effects, including stimulation of progenitor cell proliferation, regulating ductal epithelial proliferation and differentiation and ductal morphogenesis through a combination of autocrine and paracrine signaling . The respective roles of Shh and Ihh in these effects remains to be elucidated, but we have been intrigued to discover that the domain of Ihh expression coincides with the regions where tissue specific stem cells appear to be present in relative abundance . Our finding that Ihh expression is increased in response to castration suggests that Ihh is expressed by a progenitor cell population and we speculate that increased Ihh expression in the LADY tumor results from an expansion of that progenitor cell population during tumor development.
Tumor development in the LADY mouse is associated with an increased rate of epithelial proliferation at both six and 16 weeks, increased expression of progenitor cell markers (Notch-1, Nestin) and decreased expression of terminal differentiation markers (Npdc-1 and probasin). These findings are consistent with an expansion of progenitor and/or transit amplifying cell populations. FoxA proteins belong to the forkhead box a (FoxA) superfamily of transcription factors and are expressed in endodermally-derived tissues . FoxA1 immunoreactivity is found in epithelial cells of both the developing and adult prostate . We found that mRNA levels deceased significantly in the LADY tumor but that staining for FoxA1 protein was undiminished. Possible mechanisms for these findings would include increased rates of mRNA turnover or stabilization of FoxA1 protein stabilization in cells that do not udergo terminal differention. FoxA2 expression is prominent in developing bud epithelium during prostate development but localizes to basal epithelial cells of the adult periurethral ducts . FoxA2 has been detected in neuroendocrine small cell carcinomas and high Gleason grade adenocarcinomas , but FoxA2 mRNA expression was not increased in the LADY tumors,
There is no net increase in Hh signaling during tumor development in the LADY prostate cancer model. However, there is a selective and marked increase in Ihh expression even as Shh expression is decreased. Tumor development is associated with increased epithelial proliferation, increased expression on progenitor cell markers and decreased expression of terminal differentiation markers. Ihh expression may be associated with a progenitor cell population that is expanded during tumor development.
LADY mice, strain 12T-7f in a CD-1 background, were used for this study. Animals were bred, raised and sacrificed according to University of Wisconsin animal care and use guidelines. Prostate specific lobes were harvested at various times and either fixed in 10% formalin for sectioning or flash frozen for RNA isolation.
RNA isolation and Real Time-PCR
RNA was isolated using Qiagen RNeasy kit with on column DNase treatment as per manufacturer's directions. Following reverse transcription by standard protocols, gene expression was quantitated by real time PCR using Power SYBR Green PCR master mix (Applied Biosystems) on a BioRad iCycler. Expression was normalized to the internal control gene glyceraldehydes-3-phosphate dehydrogenase (GAPDH) for each gene assayed. Gene specific primer sequences are as follows:GAPDH: 5'-AGCCTCGTCCCGTAGACAAAAT-3' and 5'-CCGTGAGTG GAGTCATACTGGA-3', Shh: 5'-AATGCC TTGGCCATCTCTGT-3' and 5'GCTCGACCCTCATAGTGTAGAGACT-3', Ihh: 5'-CAGCTCACCCCCAACTACAA-3' and 5'-GAGCTCACCCCCAACTACAA-3', Ptc1: 5'-CTCTGGAGCAGATTTCCAAGG-3' and 5'-TGCCGCAGTTCTTTTGAATG-3', Gli1: 5'-GGAAGTCCTATTCACGCCTTGA-3' and 5'CAACCTTCTTGCTCACACATG TAAG-3', Igfbp-6: 5'-AGCTCCAGACTGAGGTCTTCC-3' and 5'-GAACGACACTGCTGCTTGC-3', P21: 5'-TTGCACTCTGGTGTCTGAGC-3' and 5'-TCTGCGCTTGGAGTGATAGA-3', Notch1: 5'-ACCCACTCTGTCTCCCACAC-3' and 5'-GCTTCCTTGCTACCACAAGC'-3', Nestin: 5'-GGACAGGACCAAGAGGAACA-3' and 5'-TCTGGATCCACCTTTTCTGG-3', Probasin: 5'-TCATCCTCCTGCTCACACTG-3' and 5'-AAGGCCCGTCAATCTTCTTT-3', NPDC-1: 5'-CCTCCGATGAGGAAAATGAA-3' and 5'-CGTGGAATGGTCAAACAGTG-3', FoxA1: 5'-CTCCTTATGGCGCTACCTTG-3' and 5'-AGCACGGGTCTGGAATACAC-3'.
Tissues were fixed in 10% buffered formalin overnight, followed by transfer to 50% alcohol. The paraffin-embedded tissues were sectioned (5 μm). Sections were deparaffinized and rehydrated in ethanol solutions. For FoxA1 (goat anti-FoxA1, Santa Cruz) staining, after antigen unmasking by boiling in 10 mM sodium citrate buffer (pH 6.0) for 20 min, the sections were treated with 3% hydrogen peroxide for 5 min. The following detection and visualization procedures were performed according to manufacturer's protocol (Vector Laboratories). For Ki67 staining was done at Vanderbilt Immunohistochemistry Core/Lab, the sections were rehydrated and placed in heated Target Retrieval Solution (Labvision, Fremont, CA) for 20 min. Endogenous peroxidase was neutralized with 0.03% hydrogen peroxide followed by a casein-based protein block (DakoCytomation, Carpinteria, CA) to minimize nonspecific staining. The sections were incubated with rabbit anti- Ki-67 (Vector Laboratories, Burlingame, CA) for 30 min. The Dako Envision+ HRP/DAB System (DakoCytomation) was used to produce localized, visible staining. Negative control slides were performed without primary antibodies.
Two-Way Analysis of Variance (ANOVA) was used to compare expression levels as a function of age (six vs. 16 weeks), LADY gene [(-) vs (+)] and their interaction. This was done separately for each of the proteins (Shh, Ihh, Gli 1, Ptc 1, probasin, p21, nestin, NPDC-1, IGFBP-6). The tenability of the assumptions of ANOVA was assessed with residual plots. If the assumptions of ANOVA seemed to be violated, transformations of the response were considered. If a term in the model was statistically significant, pair-wise comparisons were obtained and examined for significance; this corresponds to Fisher's protected Least Significant Difference (LSD) procedure. P < 0.05 was the criterion for statistical significance. The analyses were performed with Proc GLM, SAS v.9.1 statistical software (SAS, Cary, NC). Results: The natural logarithms of the expression levels were log-transformed prior to ANOVA in order to homogenize the variances and better meet the assumptions of ANOVA.
This work was supported in part by grants from the NIH, NCI (CA95386-01) and the DOD CDMRP (W81XWH-04-1-0263).
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