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癌症中的p21激活激酶

p21-activated kinases in cancer.

作者信息

Kumar Rakesh, Gururaj Anupama E, Barnes Christopher J

机构信息

The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030-4009, USA.

出版信息

Nat Rev Cancer. 2006 Jun;6(6):459-71. doi: 10.1038/nrc1892.

Abstract

The pivotal role of kinases in signal transduction and cellular regulation has lent them considerable appeal as pharmacological targets across a broad spectrum of cancers. p21-activated kinases (Paks) are serine/threonine kinases that function as downstream nodes for various oncogenic signalling pathways. Paks are well-known regulators of cytoskeletal remodelling and cell motility, but have recently also been shown to promote cell proliferation, regulate apoptosis and accelerate mitotic abnormalities, which results in tumour formation and cell invasiveness. Alterations in Pak expression have been detected in human tumours, which makes them an attractive new therapeutic target.

摘要

激酶在信号转导和细胞调节中起着关键作用,这使其作为广泛癌症的药理学靶点具有相当大的吸引力。p21激活激酶(Paks)是丝氨酸/苏氨酸激酶,作为各种致癌信号通路的下游节点发挥作用。Paks是众所周知的细胞骨架重塑和细胞运动的调节因子,但最近也被证明可促进细胞增殖、调节细胞凋亡并加速有丝分裂异常,从而导致肿瘤形成和细胞侵袭。在人类肿瘤中已检测到Pak表达的改变,这使其成为一个有吸引力的新治疗靶点。

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