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Notch signaling dynamics in the adult healthy prostate and in prostatic tumor development
Author(s) -
Pedrosa AnaRita,
Graça José L.,
Carvalho Sandra,
Peleteiro Maria C.,
Duarte António,
Trindade Alexandre
Publication year - 2016
Publication title -
the prostate
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.295
H-Index - 123
eISSN - 1097-0045
pISSN - 0270-4137
DOI - 10.1002/pros.23102
Subject(s) - notch signaling pathway , prostate , hes1 , tramp , stromal cell , carcinogenesis , prostate cancer , cancer research , pca3 , pathology , biology , medicine , signal transduction , microbiology and biotechnology , cancer
BACKGROUND The Notch signaling pathway has been implicated in prostate development, maintenance and tumorigenesis by its key role in cell‐fate determination, differentiation and proliferation. Therefore, we proposed to analyze Notch family members transcription and expression, including ligands (Dll1, 3, 4 and Jagged1 and 2), receptors (Notch1–4) and effectors (Hes1, 2, 5 and Hey1, 2, L), in both normal and tumor bearing mouse prostates to better understand the dynamics of Notch signaling in prostate tumorigenesis. METHODS Wild type mice and transgenic adenocarcinoma of the mouse prostate model (TRAMP) mice were sacrificed at 18, 24 or 30 weeks of age and the prostates collected and processed for either whole prostate or prostate cell specific populations mRNA analysis and for protein expression analysis by immunohistochemistry and immunofluorescence. RESULTS We observed that Dll1 and Dll4 are expressed in the luminal compartment of the mouse healthy prostate, whereas Jagged2 expression is restricted to the basal and stromal compartment. Additionally, Notch2 and Notch4 are normally expressed in the prostate luminal compartment while Notch2 and Notch3 are also expressed in the stromal layer of the healthy prostate. As prostate tumor development takes place, there is up‐regulation of Notch components. Particularly, the prostate tumor lesions have increased expression of Jagged1 and 2, of Notch3 and of Hey1. We have also detected the presence of activated Notch3 in prostatic tumors that co‐express Jagged1 and ultimately the Hey1 effector. CONCLUSIONS Taken together our results point out the Notch axis Jagged1‐2/Notch3/Hey1 to be important for prostate tumor development and worthy of additional functional studies and validation in human clinical disease. Prostate 76:80–96, 2016 . © 2015 Wiley Periodicals, Inc.