TY - JOUR
T1 - Reduced levels of transforming growth factor β receptor type II in human prostate cancer
T2 - An immunohistochemical study
AU - Williams, Russel H.
AU - Stapleton, Alan M.F.
AU - Yang, Guang
AU - Truong, Luan
AU - Rogers, Eammon
AU - Timme, Terry L.
AU - Wheeler, Thomas M.
AU - Scardino, Peter T.
AU - Thompson, Timothy C.
N1 - Copyright:
Copyright 2007 Elsevier B.V., All rights reserved.
PY - 1996/4
Y1 - 1996/4
N2 - In previous studies we demonstrated that the growth of human prostatic adenocarcinoma is associated with aberrant accumulation of transforming growth factor (TGF) β1, a growth factor that has been shown to be a potent inhibitor of epithelial cell proliferation. We investigated the expression of TGF-β receptor II (TGFβR-II) in benign prostate tissue and in prostate cancer using standard immunohistochemical techniques. Quantitation of immunopositivity for TGFβR-II was assessed on a visual analogue scale ranging from 0 (absence of staining) to 4+ (intensely positive staining). All of the benign glandular epithelia stained intensely, either 3+ or 4+, representative of the ubiquitous nature of TGFβR-II in normal tissue Overall, staining was reduced in prostate cancer sections, and there was progressively diminished staining as the histological grade of the cancer increased (P < 0.01, Kruskal-Wallis test). This immunohistochemical study indicates that a decline in the levels of TGFβR-II is correlated with advancing histological aggressiveness of the cancer and suggests that aberrant TGFβR-II function may play a role in human prostate carcinogenesis.
AB - In previous studies we demonstrated that the growth of human prostatic adenocarcinoma is associated with aberrant accumulation of transforming growth factor (TGF) β1, a growth factor that has been shown to be a potent inhibitor of epithelial cell proliferation. We investigated the expression of TGF-β receptor II (TGFβR-II) in benign prostate tissue and in prostate cancer using standard immunohistochemical techniques. Quantitation of immunopositivity for TGFβR-II was assessed on a visual analogue scale ranging from 0 (absence of staining) to 4+ (intensely positive staining). All of the benign glandular epithelia stained intensely, either 3+ or 4+, representative of the ubiquitous nature of TGFβR-II in normal tissue Overall, staining was reduced in prostate cancer sections, and there was progressively diminished staining as the histological grade of the cancer increased (P < 0.01, Kruskal-Wallis test). This immunohistochemical study indicates that a decline in the levels of TGFβR-II is correlated with advancing histological aggressiveness of the cancer and suggests that aberrant TGFβR-II function may play a role in human prostate carcinogenesis.
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M3 - Article
C2 - 9816213
AN - SCOPUS:0029991231
SN - 1078-0432
VL - 2
SP - 635
EP - 640
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 4
ER -