PI3K/AKT/mTOR通路
耐受性
乳腺癌
医学
癌症研究
临床试验
表观遗传学
蛋白激酶B
药理学
癌症
生物信息学
生物
肿瘤科
信号转导
内科学
不利影响
基因
生物化学
作者
Michael McKenna,Sarah A. McGarrigle,Graham P. Pidgeon
标识
DOI:10.1016/j.bbcan.2018.08.001
摘要
The PI3K/Akt/mTOR pathway plays a role in various oncogenic processes in breast cancer and key pathway aberrations have been identified which drive the different molecular subtypes. Early drugs developed targeting this pathway produced some clinical success but were hampered by pharmacokinetics, tolerability and efficacy problems. This created a need for new PI3K pathway-inhibiting drugs, which would produce more robust results allowing incorporation into treatment regimens for breast cancer patients. In this review, the most promising candidates from the new generation of PI3K-pathway inhibitors is explored, presenting evidence from preclinical and early clinical research, as well as ongoing trials utilising these drugs in breast cancer cohorts. The problems hindering the development of drugs targeting the PI3K pathway are examined, which have created problems for their use as monotherapies. PI3K pathway inhibitor combinations therefore remains a dynamic research area, and their role in combination with immunotherapies and epigenetic therapies is also inspected.
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