Targeting PI3K/Akt/mTOR signaling pathway in the treatment of prostate cancer radioresistance

被引:176
作者
Chang, Lei [1 ,2 ,3 ]
Graham, Peter H. [1 ,2 ,3 ]
Ni, Jie [1 ,2 ,3 ]
Hao, Jingli [1 ,2 ,3 ]
Bucci, Joseph [1 ,2 ,3 ]
Cozzi, Paul J. [3 ,4 ]
Li, Yong [1 ,2 ,3 ]
机构
[1] St George Hosp, Canc Care Ctr, Sydney, NSW, Australia
[2] St George Hosp, Prostate Canc Inst, Sydney, NSW, Australia
[3] Univ New S Wales, Fac Med, St George & Sutherland Clin Sch, Kensington, NSW 2033, Australia
[4] St George Hosp, Dept Surg, Kogarah, NSW 2217, Australia
关键词
Prostate cancer; Radiation therapy; Radioresistance; Inhibitors; PI3K/Akt/mTOR; DUAL PI3K/MTOR INHIBITOR; PHOSPHATIDYLINOSITOL 3-KINASE/MAMMALIAN TARGET; PROTEIN-KINASE-B; I PI3 KINASE; RADIATION-THERAPY; PALOMID; 529; PHASE-II; TORC1/TORC2; INHIBITOR; RAPAMYCIN INHIBITOR; TUMOR ANGIOGENESIS;
D O I
10.1016/j.critrevonc.2015.07.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:507 / 517
页数:11
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