RAS和SHOC2在RAF激活和治疗中的作用

Daniel A. Bonsor, Dhirendra K. Simanshu
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引用次数: 0

摘要

RAS蛋白的突变在人类癌症的发展中起着关键作用,驱动持续的RAF激活和解除对丝裂原活化蛋白激酶(MAPK)信号通路的调节。虽然在靶向特异性致癌RAS蛋白方面取得了进展,但针对大多数RAS突变的有效药物治疗仍然有限。最近对RAS-RAF复合物和SHOC2-MRAS-PP1C全酶复合物的研究为MAPK信号通路中RAF激活的结构和功能方面提供了重要的见解。此外,这些研究还揭示了开发抑制剂的新蓝图,使我们能够超越当前的RAS和MEK抑制剂。在这篇综述中,我们探讨了RAS和SHOC2在激活RAF中的作用,并讨论了针对这些蛋白的潜在治疗策略。全面了解RAF活化过程中涉及的分子相互作用及其治疗意义,可以潜在地推动对抗RAS-/RAF驱动的癌症的创新方法。预计《癌症生物学年度评论》第8卷的最终在线出版日期是2024年4月。修订后的估计数请参阅http://www.annualreviews.org/page/journal/pubdates。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RAS and SHOC2 Roles in RAF Activation and Therapeutic Considerations
Mutations in RAS proteins play a pivotal role in the development of human cancers, driving persistent RAF activation and deregulating the mitogen-activated protein kinase (MAPK) signaling pathway. While progress has been made in targeting specific oncogenic RAS proteins, effective drug-based therapies for most RAS mutations remain limited. Recent investigations into RAS–RAF complexes and the SHOC2–MRAS–PP1C holoenzyme complex have provided crucial insights into the structural and functional aspects of RAF activation within the MAPK signaling pathway. Moreover, these studies have also unveiled new blueprints for developing inhibitors, allowing us to think beyond the current RAS and MEK inhibitors. In this review, we explore the roles of RAS and SHOC2 in activating RAF and discuss potential therapeutic strategies to target these proteins. A comprehensive understanding of the molecular interactions involved in RAF activation and their therapeutic implications can potentially drive innovative approaches in combating RAS-/RAF-driven cancers.Expected final online publication date for the Annual Review of Cancer Biology, Volume 8 is April 2024. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.
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