癌症、致癌原因和治疗方法综述:PIK3 通路对癌症的作用

Choudhary Ml
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引用次数: 0

摘要

磷酸肌酸 3-激酶(PI3K)活化在肿瘤细胞生物学中的核心功能促使人们在癌症中针对 PI3K 和/或类似 AKT 和哺乳动物雷帕霉素靶标(mTOR)的下游激酶进行大量研究。然而,已有的临床数据显示,针对 PI3K、AKT 或 mTOR 的抑制剂在允许剂量下的单药作用有限。一个例外是习惯性淋巴细胞白血病患者对PI3Kδ抑制剂的反应,在这种情况下,细胞天然调节和外来调节相结合会产生疗效。然后,我们回顾了针对 PI3K - AKT - mTOR 通路的抑制剂临床开发所面临的关键挑战和机遇。通过减少对患者选择的关注、增加对脆弱调节的了解以及合理组合的战略操作,应该有可能实现这类前景光明的靶向抗癌药物的最终目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review on Cancer, Cause of Cancer and Treatment: Role of PIK3 Pathway on Cancer
The central function of phosphoinositide 3- kinase (PI3K) activation in tumour cell biology has urged a sizeable trouble to target PI3K and/ or downstream kinases similar as AKT and mammalian target of rapamycin (mTOR) in cancer. still, arising clinical data show limited single- agent exertion of impediments targeting PI3K, AKT or mTOR at permitted boluses. One exception is the response to PI3Kδ impediments in habitual lymphocytic leukaemia, where a combination of cell- natural and- foreign conditioning drive efficacity. Then, we review crucial challenges and openings for the clinical development of impediments targeting the PI3K – AKT – mTOR pathway. Through a lesser focus on patient selection, increased understanding of vulnerable modulation and strategic operation of rational combinations, it should be possible to realize the eventuality of this promising class of targeted anticancer agents.
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