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p21-激活的激酶作为血液系统恶性肿瘤有前途的治疗靶点。

p21-Activated kinases as promising therapeutic targets in hematological malignancies.

机构信息

Terry Fox Laboratory, British Columbia Cancer Research Institute, Vancouver, BC, Canada.

Interdisciplinary Oncology, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

出版信息

Leukemia. 2022 Feb;36(2):315-326. doi: 10.1038/s41375-021-01451-7. Epub 2021 Oct 25.

Abstract

The p21-Activated Kinases (PAKs) are a family of six serine/threonine kinases that were originally identified as downstream effectors of the Rho GTPases Cdc42 and Rac. Since the first PAK was discovered in 1994, studies have revealed their fundamental and biological importance in the development of physiological systems. Within the cell, PAKs also play significant roles in regulating essential cellular processes such as cytoskeletal dynamics, gene expression, cell survival, and cell cycle progression. These processes are often deregulated in numerous cancers when different PAKs are overexpressed or amplified at the chromosomal level. Furthermore, PAKs modulate multiple oncogenic signaling pathways which facilitate apoptosis escape, uncontrolled proliferation, and drug resistance. There is growing insight into the critical roles of PAKs in regulating steady-state hematopoiesis, including the properties of hematopoietic stem cells (HSC), and the initiation and progression of hematological malignancies. This review will focus on the most recent studies that provide experimental evidence showing how specific PAKs regulate the properties of leukemic stem cells (LSCs) and drug-resistant cells to initiate and maintain hematological malignancies. The current understanding of the molecular and cellular mechanisms by which the PAKs operate in specific human leukemia or lymphomas will be discussed. From a translational point of view, PAKs have been suggested to be critical therapeutic targets and potential prognosis markers; thus, this review will also discuss current therapeutic strategies against hematological malignancies using existing small-molecule PAK inhibitors, as well as promising combination treatments, to sensitize drug-resistant cells to conventional therapies. The challenges of toxicity and non-specific targeting associated with some PAK inhibitors, as well as how future approaches for PAK inhibition to overcome these limitations, will also be addressed.

摘要

p21 激活激酶(PAKs)是一个家族的六种丝氨酸/苏氨酸激酶,最初被鉴定为 Rho GTPases Cdc42 和 Rac 的下游效应物。自 1994 年首次发现 PAK 以来,研究揭示了它们在生理系统发育中的基本和生物学重要性。在细胞内,PAKs 还在调节细胞骨架动力学、基因表达、细胞存活和细胞周期进程等基本细胞过程中发挥重要作用。当不同的 PAK 在染色体水平上过度表达或扩增时,这些过程通常在许多癌症中失调。此外,PAKs 调节多种致癌信号通路,促进细胞凋亡逃逸、不受控制的增殖和耐药性。越来越多的证据表明 PAK 在调节稳态造血中起关键作用,包括造血干细胞(HSC)的特性,以及血液恶性肿瘤的起始和进展。这篇综述将重点介绍最近的研究,这些研究提供了实验证据,表明特定的 PAK 如何调节白血病干细胞(LSCs)和耐药细胞的特性,以启动和维持血液恶性肿瘤。还将讨论目前对 PAK 在特定人类白血病或淋巴瘤中的作用的分子和细胞机制的理解。从转化的角度来看,PAKs 被认为是关键的治疗靶点和潜在的预后标志物;因此,本综述还将讨论使用现有的小分子 PAK 抑制剂针对血液恶性肿瘤的当前治疗策略,以及有前途的联合治疗方法,以使耐药细胞对常规治疗敏感。还将解决一些 PAK 抑制剂与毒性和非特异性靶向相关的挑战,以及未来的 PAK 抑制方法如何克服这些限制。

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