| Literature DB >> 29858226 |
Joanna Triscott1, Mark A Rubin2,3.
Abstract
<b/> PI3K pathway alterations are frequently recurrent in metastatic prostate cancer and are associated with the development of currently incurable castration-resistant disease. Candidate inhibitors that target single PI3K pathway members lack efficacy as demonstrated in multiple clinical trials. In this issue, Pearson and colleagues examine the functional importance of co-occurring PIK3CA and PTEN aberrations using a novel mouse model and demonstrate a synergistic acceleration of tumorigenesis that may be responsible for de novo metastatic prostate cancer. Cancer Discov; 8(6); 682-5. ©2018 AACRSee related article by Pearson et al., p. 764. ©2018 American Association for Cancer Research.Entities:
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Year: 2018 PMID: 29858226 DOI: 10.1158/2159-8290.CD-18-0369
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397