XIAP as target for therapeutic apoptosis in prostate cancer.

Journal Article (Journal Article;Review)

Progression to androgen independence combined with chemotherapy resistance remains one of the primary obstacles to the improvement of quality of life and survival for patients with advanced prostate cancer. One unique feature of the androgen-independent cell population is that they still retain the appropriate machinery for apoptosis. Therefore, identifying a cure for prostate cancer requires identification and reversal of the antiapoptotic mechanisms responsible for drug resistance and/or newer therapies that bypass the apoptosis-resistance pathways. The key element in the apoptotic pathway is the processing and activation of caspases by either a mitochondrial-dependent or -independent cascade of events. XIAP, a member of the inhibitor of apoptosis family of proteins (IAP), has been identified as a potent caspase inhibitor. XIAP expression seems to be regulated by the presence of a rare sequence, internal ribosome entry sequence (IRES) in its 5' untranslated region (5' UTR) which facilitates its antiapoptotic function during any kind of induced-cellular stress like radiation and chemotherapy, making it an attractive therapeutic target. This review attempts to present an overview of the interaction between cell survival and death pathways, mechanism of XIAP action and recent studies supporting XIAP as an emerging therapeutic target.

Full Text

Duke Authors

Cited Authors

  • Devi, GR

Published Date

  • March 2004

Published In

Volume / Issue

  • 17 / 2

Start / End Page

  • 127 - 134

PubMed ID

  • 15098067

International Standard Serial Number (ISSN)

  • 0214-0934

Digital Object Identifier (DOI)

  • 10.1358/dnp.2004.17.2.829046


  • eng

Conference Location

  • United States