血管生成
激酶
癌症
生物
重编程
CDC42型
癌症研究
RAC1
转移
蛋白激酶A
细胞生物学
计算生物学
信号转导
细胞
生物化学
遗传学
作者
Yixi Yuan,Hongyan Zhang,Danni Li,Ying Liu,Fengzhan Lin,Yanzhi Wang,Hui Song,Xu Liu,Lian‐Shun Feng,Jian Zhang
出处
期刊:Cancer Letters
[Elsevier]
日期:2022-10-01
卷期号:545: 215813-215813
被引量:9
标识
DOI:10.1016/j.canlet.2022.215813
摘要
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.
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