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Akt in Prostate Cancer: Possible Role in Androgen-Independence

[ Vol. 4 , Issue. 6 ]

Author(s):

Paramita M. Ghosh, Shazli Malik, Roble Bedolla and Jeffrey I. Kreisberg   Pages 487 - 496 ( 10 )

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).

Keywords:

akt, pi3k, androgen receptor, mapk, pten, prostate cancer

Affiliation:

Department of Surgery, The University of Texas Health Science Center at San Antonio, 7703 Floyd CurlDrive, San Antonio, TX 78229-3900, USA.



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