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靶向PI3K/Akt信号通路治疗胃癌:个性化医疗的现实选择?

Targeting the PI3K/Akt signaling pathway in gastric carcinoma: A reality for personalized medicine?

作者信息

Singh Shikha Satendra, Yap Wei Ney, Arfuso Frank, Kar Shreya, Wang Chao, Cai Wanpei, Dharmarajan Arunasalam M, Sethi Gautam, Kumar Alan Prem

机构信息

Shikha Satendra Singh, Wei Ney Yap, Shreya Kar, Chao Wang, Wanpei Cai, Gautam Sethi, Alan Prem Kumar, Cancer Science Institute of Singapore, National University of Singapore, Singapore City 117597, Singapore.

出版信息

World J Gastroenterol. 2015 Nov 21;21(43):12261-73. doi: 10.3748/wjg.v21.i43.12261.

Abstract

Frequent activation of phosphatidylinositol-3 kinases (PI3K)/Akt/mTOR signaling pathway in gastric cancer (GC) is gaining immense popularity with identification of mutations and/or amplifications of PIK3CA gene or loss of function of PTEN, a tumor suppressor protein, to name a few; both playing a crucial role in regulating this pathway. These aberrations result in dysregulation of this pathway eventually leading to gastric oncogenesis, hence, there is a need for targeted therapy for more effective anticancer treatment. Several inhibitors are currently in either preclinical or clinical stages for treatment of solid tumors like GC. With so many inhibitors under development, further studies on predictive biomarkers are needed to measure the specificity of any therapeutic intervention. Herein, we review the common dysregulation of PI3K/Akt/mTOR pathway in GC and the various types of single or dual pathway inhibitors under development that might have a superior role in GC treatment. We also summarize the recent developments in identification of predictive biomarkers and propose use of predictive biomarkers to facilitate more personalized cancer therapy with effective PI3K/Akt/mTOR pathway inhibition.

摘要

随着PIK3CA基因的突变和/或扩增、肿瘤抑制蛋白PTEN功能丧失等情况的发现,磷脂酰肌醇-3激酶(PI3K)/蛋白激酶B(Akt)/哺乳动物雷帕霉素靶蛋白(mTOR)信号通路在胃癌(GC)中的频繁激活日益受到关注;这些情况在调节该信号通路中都起着关键作用。这些异常导致该信号通路失调,最终引发胃癌发生,因此,需要进行靶向治疗以实现更有效的抗癌治疗。目前有几种抑制剂正处于治疗GC等实体瘤的临床前或临床阶段。鉴于有如此多的抑制剂正在研发中,需要对预测性生物标志物进行进一步研究,以衡量任何治疗干预的特异性。在此,我们综述了PI3K/Akt/mTOR信号通路在GC中的常见失调情况以及正在研发的各种类型的单通路或双通路抑制剂,这些抑制剂可能在GC治疗中发挥更卓越的作用。我们还总结了预测性生物标志物识别方面的最新进展,并建议使用预测性生物标志物来促进通过有效抑制PI3K/Akt/mTOR信号通路实现更个性化的癌症治疗。

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