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PAK4 在癌症发展中的作用:新兴的参与者和治疗机会。

PAK4 in cancer development: Emerging player and therapeutic opportunities.

机构信息

Department of Cell Biology, Key Laboratory of Cell Biology, National Health Commission of the PR China, Key Laboratory of Medical Cell Biology, Ministry of Education of the PR China, China Medical University, No. 77, Puhe Road, Shenyang North New Area, Shenyang, Liaoning, 110122, China.

Department of Medical Oncology, First Affiliated Hospital of China Medical University, Key Laboratory of Anticancer Drugs and Biotherapy of Liaoning Province, Liaoning Province Clinical Research Center for Cancer; No. 155, North Nanjing Street, Shenyang, Liaoning, 110001, China.

出版信息

Cancer Lett. 2022 Oct 1;545:215813. doi: 10.1016/j.canlet.2022.215813. Epub 2022 Jul 4.

Abstract

p21-activated kinase 4 (PAK4), a member of the serine-threonine kinase family, was initially identified as a protein kinase that functions downstream of the Rho GTPases cdc42 and Rac1. Recently, it has been proven that PAK4 not only regulates many cellular physiological processes, but also plays an important role in the occurrence and development of various cancers. Here, we provide a systematic overview of PAK4, including its structure, localization, expression and aberration, upstream regulators, and key functions in almost every aspect of cancer hallmarks, including cancer cell proliferation, invasion and metastasis, angiogenesis, metabolism reprogramming, and immune escape. Subsequently, we also discuss the existing small molecule PAK4 inhibitors according to their structure types and their potential applications in cancer treatment. We hope our systematic review will provide the most comprehensive description of the current advancements in PAK4 research and new enlightenment for the individualized diagnosis and treatment of cancer.

摘要

p21 激活激酶 4(PAK4)是丝氨酸/苏氨酸激酶家族的成员,最初被鉴定为一种蛋白激酶,其在 Rho GTPases cdc42 和 Rac1 的下游发挥作用。最近,已经证明 PAK4 不仅调节许多细胞生理过程,而且在各种癌症的发生和发展中也起着重要作用。在这里,我们对 PAK4 进行了系统概述,包括其结构、定位、表达和异常、上游调节剂以及在癌症特征的几乎所有方面的关键功能,包括癌细胞增殖、侵袭和转移、血管生成、代谢重编程和免疫逃逸。随后,我们还根据结构类型讨论了现有的小分子 PAK4 抑制剂及其在癌症治疗中的潜在应用。我们希望我们的系统综述将为 PAK4 研究的最新进展提供最全面的描述,并为癌症的个体化诊断和治疗提供新的启示。

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