Targeting the PI3K/Akt/mTOR pathway in non-small cell lung cancer (NSCLC)

被引:367
|
作者
Tan, Aaron C. [1 ]
机构
[1] Natl Canc Ctr Singapore, Div Med Oncol, 11 Hosp Crescent, Singapore 169610, Singapore
关键词
Akt pathway; mTOR pathway; non-small cell lung cancer; PI3K pathway; targeted therapy; I PI3K INHIBITOR; TUMOR-SUPPRESSOR; PIK3CA GENE; PHOSPHOINOSITIDE; 3-KINASE; MAMMALIAN TARGET; COPY NUMBER; PHASE-II; PICTILISIB GDC-0941; PTEN EXPRESSION; DOSE-ESCALATION;
D O I
10.1111/1759-7714.13328
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The traditional classification of lung cancer into small cell lung cancer and non-small cell lung cancer (NSCLC) has been transformed with the increased understanding of the molecular alterations and genomic biomarkers that drive the development of lung cancer. Increased activation of the phosphatidylinositol 3-kinase (PI3K)/Akt/mechanistic target of rapamycin (mTOR) pathway leads to numerous hallmarks of cancer and this pathway represents an attractive target for novel anticancer therapies. In NSCLC, the PI3K/Akt/mTOR pathway has been heavily implicated in both tumorigenesis and the progression of disease. A number of specific inhibitors of PI3K, Akt and mTOR are currently under development and in various stages of preclinical investigation and in early phase clinical trials for NSCLC. Early evidence has yielded disappointing results. Clinical trials, however, have been performed on predominantly molecularly unselected populations, and patient enrichment strategies using high-precision predictive biomarkers in future trials will increase the likelihood of success. A greater understanding of the underlying molecular biology including epigenetic alterations is also crucial to allow for the detection of appropriate biomarkers and guide combination approaches.
引用
收藏
页码:511 / 518
页数:8
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