PI3K/AKT/mTOR通路
癌症治疗
癌症
医学
癌症研究
生物信息学
药理学
信号转导
生物
内科学
生物化学
作者
Pau Castel,Eneda Toska,Jeffrey A. Engelman,Maurizio Scaltriti
出处
期刊:Nature cancer
[Springer Nature]
日期:2021-06-17
卷期号:2 (6): 587-597
被引量:95
标识
DOI:10.1038/s43018-021-00218-4
摘要
Phosphoinositide 3-kinase (PI3K) signaling regulates cellular proliferation, survival and metabolism, and its aberrant activation is one of the most frequent oncogenic events across human cancers. In the last few decades, research has focused on the development of PI3K inhibitors, from preclinical tool compounds to the highly specific medicines approved to treat patients with cancer. Herein we discuss current paradigms for PI3K inhibitors in cancer therapy, focusing on clinical data and mechanisms of action. We also discuss current limitations in the use of PI3K inhibitors, including toxicities and mechanisms of resistance, with specific emphasis on approaches aimed at improving efficacy. Scatiltri and colleagues review the paradigms of targeting PI3K in solid tumors in the clinic, including the progress so far in developing effective inhibitors as well as clinical limitations due to toxicity and therapeutic resistance.
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