Bonsor Daniel A, Simanshu Dhirendra K
NCI RAS Initiative, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Annu Rev Cancer Biol. 2024 Jun;8:97-113. doi: 10.1146/annurev-cancerbio-062822-030450. Epub 2023 Dec 5.
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 the majority of RAS mutations remain limited. Recent investigations on 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 holds the potential to drive innovative approaches in combating RAS/RAF-driven cancers.
RAS蛋白突变在人类癌症发展中起关键作用,驱动RAF持续激活并使丝裂原活化蛋白激酶(MAPK)信号通路失调。虽然在靶向特定致癌RAS蛋白方面已取得进展,但针对大多数RAS突变的有效药物疗法仍然有限。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,使我们能够超越目前的RAS和MEK抑制剂进行思考。在本综述中,我们探讨了RAS和SHOC2在激活RAF中的作用,并讨论了靶向这些蛋白的潜在治疗策略。全面了解RAF激活中涉及的分子相互作用及其治疗意义,有可能推动对抗RAS/RAF驱动癌症的创新方法。