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Curr Drug Metab. 2003 Dec;4(6):487-96.

Akt in prostate cancer: possible role in androgen-independence.

Author information

1
Department of Surgery, University of Texas Health Science Center at San Antonio and South Texas Veterans Health Care System, Audie L. Murphy Veterans Administration Hospital, San Antonio, TX 78229-3900, USA.

Abstract

Akt, a downstream effector of phosphatidylinositol 3-kinase (PI3K), has often been implicated in prostate cancer. Studies in prostate tumor cell lines revealed that Akt activation is probably important for the progression of prostate cancer to an androgen-independent state. Investigations of human prostate cancer tissues show that although there is neither Akt gene amplification nor enhanced protein expression in prostate cancer compared to normal tissue, poorly differentiated tumors exhibit increased expression of a phosphorylated (activated) form of Akt compared to normal tissue, prostatic intraepithelial neoplasia (PIN) or well-differentiated prostate cancer. Akt phosphorylation is accompanied by the inactivation of ERK, a member of the mitogen activated protein kinase (MAPK) family. In this article, we postulate that Akt promotes androgen-independent survival of prostate tumor cells by modulating the expression and activation of the androgen receptor (AR).

PMID:
14683476
DOI:
10.2174/1389200033489226
[Indexed for MEDLINE]

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