| Literature DB >> 26253360 |
Lei Chang1, Peter H Graham1, Jie Ni1, Jingli Hao1, Joseph Bucci1, Paul J Cozzi2, Yong Li3.
Abstract
The phosphatidylinositol-3-kinase/Akt and the mammalian target of rapamycin (PI3K/Akt/mTOR) pathway is one of the most frequently activated signaling pathways in prostate cancer (CaP) and other cancers, and responsible for the survival, metastasis and therapeutic resistance. Recent advances in radiation therapy indicate that activation of this pathway is closely associated with cancer radioresistance, which is a major challenge for the current CaP radiation treatment. Therefore, targeting this pathway by inhibitors to enhance radiosensitivity has great potential for clinical benefits of CaP patients. In this review, we summarize the recent findings in the PI3K/Akt/mTOR pathway in CaP radiotherapy research and discuss the potential use of the PI3K/Akt/mTOR pathway inhibitors as radiosensitizers in the treatment of CaP radioresistance in preclinical studies to explore novel approaches for future clinical trials.Entities:
Keywords: Inhibitors; PI3K/Akt/mTOR; Prostate cancer; Radiation therapy; Radioresistance
Mesh:
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Year: 2015 PMID: 26253360 DOI: 10.1016/j.critrevonc.2015.07.005
Source DB: PubMed Journal: Crit Rev Oncol Hematol ISSN: 1040-8428 Impact factor: 6.312