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癌症治疗中基于原理的PI3K抑制剂治疗组合

Rationale-based therapeutic combinations with PI3K inhibitors in cancer treatment.

作者信息

Castel Pau, Toska Eneda, Zumsteg Zachary S, Carmona F Javier, Elkabets Moshe, Bosch Ana, Scaltriti Maurizio

机构信息

Human Oncology & Pathogenesis Program (HOPP); Memorial Sloan Kettering Cancer Center ; New York, NY USA.

出版信息

Mol Cell Oncol. 2014 Oct 29;1(3):e963447. doi: 10.4161/23723548.2014.963447. eCollection 2014 Jul-Sep.

Abstract

The PI3K/AKT/mTOR signaling is important for cell proliferation, survival, and metabolism. Hyperactivation of this pathway is one of the most common signaling abnormalities observed in cancer and a substantial effort has recently been made to develop molecules targeting this signaling cascade. However, it is becoming evident that PI3K inhibitors used as single agents do not elicit dramatic or durable responses. Given the numerous mechanisms mediating intrinsic and acquired resistance to these agents, hypothesis-based combinatorial strategies are probably needed to fully exploit their antitumor activity. In the first part of this review, we briefly dissect the PI3K/AKT/mTOR axis and list the most advanced compounds targeting different nodes of this cascade. The second part focuses on what we believe to be the most promising rationale-based therapeutic combinations with PI3K/AKT/mTOR inhibitors in solid tumors, with special emphasis on breast cancer.

摘要

PI3K/AKT/mTOR信号传导对于细胞增殖、存活和代谢至关重要。该信号通路的过度激活是癌症中最常见的信号异常之一,最近人们为开发靶向这一信号级联反应的分子付出了巨大努力。然而,越来越明显的是,单独使用PI3K抑制剂并不能引发显著或持久的反应。鉴于介导对这些药物的内在和获得性耐药的机制众多,可能需要基于假设的联合策略来充分发挥其抗肿瘤活性。在本综述的第一部分,我们简要剖析PI3K/AKT/mTOR轴,并列出靶向该信号级联不同节点的最先进化合物。第二部分重点讨论我们认为在实体瘤中与PI3K/AKT/mTOR抑制剂最有前景的基于理论的治疗组合,特别强调乳腺癌。

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2
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Cancer Cell. 2014 Jul 14;26(1):136-49. doi: 10.1016/j.ccr.2014.05.020. Epub 2014 Jul 4.
7
PI3K and cancer: lessons, challenges and opportunities.
Nat Rev Drug Discov. 2014 Feb;13(2):140-56. doi: 10.1038/nrd4204.

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