| Literature DB >> 25374921 |
Benyi Li1, Aijing Sun2, Wencong Jiang3, J Brantley Thrasher4, Paul Terranova5.
Abstract
Prostate cancers in the castration-resistant stage are life-threatening because they are not curable in clinic. The novel androgen receptor inhibitor Xandi (Enzalutamide) and the new CYP17 inhibitor Zytiga (Abiraterone) prolonged patient survival only a few months in advanced prostate cancers. Therefore, novel therapeutic agents for advanced prostate cancers are urgently needed. PI-3 kinases are major intracellular signaling molecules that regulate multiple signal pathways related to cellular metabolism, cytokinesis, growth and survival. Accumulating evidence in the literature indicates that some isoforms of this kinase family are oncogenic and abnormally expressed in various human cancers, including prostate cancers. Recent extensive studies from our group and others showed that PI-3 kinase p110β is aberrantly overexpressed in advanced prostate cancers and is critical for prostate cancer development and progression as demonstrated in cell-based and animal models. Importantly, novel p110β-specific inhibitors have been developed and are currently been testing in clinical trials. In this article, we will briefly summarize recent developments in this regard.Entities:
Keywords: Prostate cancer; cancer therapy; castration resistance; p110β
Year: 2014 PMID: 25374921 PMCID: PMC4219313
Source DB: PubMed Journal: Am J Clin Exp Urol ISSN: 2330-1910