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靶向急性髓系白血病中的PI3K/AKT信号传导和DNA损伤反应:增强化疗反应并克服耐药性的新型治疗策略

Targeting of PI3K/AKT signaling and DNA damage response in acute myeloid leukemia: a novel therapeutic strategy to boost chemotherapy response and overcome resistance.

作者信息

Estruch Montserrat, Vittori Camilla, Montesinos Teresa Muñoz, Reckzeh Kristian, Theilgaard-Mönch Kim

机构信息

The Finsen Laboratory, Rigshospitalet/National University Hospital, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen DK-2200, Denmark.

Biotech Research and Innovation Centre, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen DK-2200, Denmark.

出版信息

Cancer Drug Resist. 2021 Nov 10;4(4):984-995. doi: 10.20517/cdr.2021.76. eCollection 2021.

Abstract

Resistance of cancer patients to DNA damaging radiation therapy and chemotherapy remains a major problem in the clinic. The current review discusses the molecular mechanisms of therapy resistance in acute myeloid leukemia (AML) conferred by cooperative chemotherapy-induced DNA damage response (DDR) and mutational activation of PI3K/AKT signaling. In addition, strategies to overcome resistance are discussed, with particular focus on studies underpinning the vast potential of therapies combining standard chemotherapy AML regimens with small molecule inhibitors targeting key regulatory hubs at the interface of DDR and oncogenic signaling pathways.

摘要

癌症患者对DNA损伤性放疗和化疗的耐药性仍是临床上的一个主要问题。本综述讨论了急性髓系白血病(AML)中由联合化疗诱导的DNA损伤反应(DDR)和PI3K/AKT信号通路的突变激活所导致的治疗耐药性的分子机制。此外,还讨论了克服耐药性的策略,特别关注了一些研究,这些研究支持了将标准化疗AML方案与靶向DDR和致癌信号通路界面关键调控枢纽的小分子抑制剂相结合的疗法的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c7c/8992442/f58b4a5582ff/cdr-4-984.fig.1.jpg

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