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Expression of hedgehog pathway components in prostate carcinoma microenvironment: shifting the balance towards autocrine signalling
Author(s) -
Tzelepi Vassiliki,
Karlou Maria,
Wen Sijin,
Hoang Anh,
Logothetis Christopher,
Troncoso Patricia,
Efstathiou Eleni
Publication year - 2011
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/j.1365-2559.2011.03860.x
Subject(s) - gli1 , autocrine signalling , stromal cell , paracrine signalling , hedgehog signaling pathway , cancer research , prostate , prostate cancer , sonic hedgehog , biology , smoothened , pathology , tissue microarray , bone marrow , cancer , medicine , immunohistochemistry , signal transduction , receptor , microbiology and biotechnology
Tzelepi V, Karlou M, Wen S, Hoang A, Logothetis C, Troncoso P & Efstathiou E
(2011) Histopathology 58, 1037–1047
Expression of hedgehog pathway components in prostate carcinoma microenvironment: shifting the balance towards autocrine signalling Aims: The hedgehog (Hh) signalling pathway has been implicated in the pathogenesis and aggressiveness of prostate cancer through epithelial–mesenchymal interactions. The aim of this study was to elucidate the cell‐type partitioned expression of the Hh pathway biomarkers in the non‐neoplastic and tumour microenvironments and to correlate it with the grade and stage of prostate cancer. Methods and results: Expression of the Hh pathway components (Shh, Smo, Ptch, Gli1) in the microenvironment of non‐neoplastic peripheral zone ( n = 119), hormone‐naive primary prostate carcinoma ( n = 141) and castrate‐resistant bone marrow metastases ( n = 53) was analysed using immunohistochemistry in tissue microarrays and bone marrow sections. Results showed that epithelial Shh, Smo and Ptch expression was up‐regulated, whereas stromal Smo, Ptch, and Gli1 expression was down‐regulated in prostate carcinomas compared to non‐neoplastic peripheral zone tissue. Ptch expression was modulated further in high‐grade and high‐stage primary tumours and in bone marrow metastases. Hh signalling correlated with ki67 and vascular endothelial growth factor (VEGF) but not with CD31 expression. Conclusion: Our results highlight the importance of Hh‐mediated epithelial–mesenchymal interactions in the non‐neoplastic prostate and imply that shifting the balance from paracrine towards autocrine signalling is important in the pathogenesis and progression of prostate carcinoma.