RSK2 and its binding partners: an emerging signaling node in cancers

IF 6.9 3区 医学 Q1 CHEMISTRY, MEDICINAL
Hye Suk Lee, Sung-Jun Cho, Han Chang Kang, Joo Young Lee, Young Jik Kwon, Yong-Yeon Cho
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引用次数: 0

Abstract

The growth factor-mediated mitogen-activated protein kinase (MAPK) signaling pathways in cancer development have become increasingly important in the discovery of therapeutic agents for the treatment of cancer. RSK2 has been historically overlooked in studies regarding its involvement in physiology and signaling pathways related to human diseases, except for Coffin-Lowry syndrome, because it is located downstream of ERKs. For the last 25 years, the authors’ laboratory has made groundbreaking discoveries regarding the role of RSK2, especially by elucidating its binding partners, signaling network, and crosstalk. RSK2 is an important emerging target for developing anticancer drugs. Nevertheless, further studies on the detailed mechanism and signaling network are necessary to avoid the unexpected effects of RSK2 inhibitors. This paper describes a new paradigm of RSK2, where it works as a signaling node to modulate diverse cellular processes, including cell proliferation and transformation, cell cycle regulation, chromatin remodeling, and immune response and inflammation regulation.

RSK2及其结合伙伴:癌症中新出现的信号节点
肿瘤发展中生长因子介导的丝裂原活化蛋白激酶(MAPK)信号通路在发现治疗癌症的药物中变得越来越重要。除了Coffin-Lowry综合征外,RSK2在与人类疾病相关的生理和信号通路的研究中一直被忽视,因为它位于ERKs的下游。在过去的25年里,作者的实验室在RSK2的作用方面取得了突破性的发现,特别是通过阐明其结合伙伴,信号网络和串扰。RSK2是开发抗癌药物的重要新靶点。然而,为了避免RSK2抑制剂的意外作用,有必要进一步研究其详细的机制和信号网络。本文描述了RSK2的一个新范式,它作为一个信号节点调节多种细胞过程,包括细胞增殖和转化、细胞周期调节、染色质重塑、免疫反应和炎症调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
13.40
自引率
9.00%
发文量
48
审稿时长
3.3 months
期刊介绍: Archives of Pharmacal Research is the official journal of the Pharmaceutical Society of Korea and has been published since 1976. Archives of Pharmacal Research is an interdisciplinary journal devoted to the publication of original scientific research papers and reviews in the fields of drug discovery, drug development, and drug actions with a view to providing fundamental and novel information on drugs and drug candidates.
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