Healy Fiona M, Turner Amy L, Marensi Vanessa, MacEwan David J
Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Department of Biochemistry, Cell and Systems Biology, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, United Kingdom.
Front Pharmacol. 2024 Sep 20;15:1441938. doi: 10.3389/fphar.2024.1441938. eCollection 2024.
It is widely acknowledged that there is a considerable number of oncogenic mutations within the Ras superfamily of small GTPases which are the driving force behind a multitude of cancers. Ras proteins mediate a plethora of kinase pathways, including the MAPK, PI3K, and Ral pathways. Since Ras was considered undruggable until recently, pharmacological targeting of pathways downstream of Ras has been attempted to varying success, though drug resistance has often proven an issue. Nuances between kinase pathway activation in the presence of various Ras mutants are thought to contribute to the resistance, however, the reasoning behind activation of different pathways in different Ras mutational contexts is yet to be fully elucidated. Indeed, such disparities often depend on cancer type and disease progression. However, we are in a revolutionary age of Ras mutant targeted therapy, with direct-targeting KRAS-G12C inhibitors revolutionising the field and achieving FDA-approval in recent years. However, these are only beneficial in a subset of patients. Approximately 90% of Ras-mutant cancers are not KRAS-G12C mutant, and therefore raises the question as to whether other distinct amino acid substitutions within Ras may one day be targetable in a similar manner, and indeed whether better understanding of the downstream pathways these various mutants activate could further improve therapy. Here, we discuss the favouring of kinase pathways across an array of Ras-mutant oncogenic contexts and assess recent advances in pharmacological targeting of various Ras mutants. Ultimately, we will examine the utility of individualised pharmacological approaches to Ras-mediated cancer.
人们普遍认为,小GTP酶的Ras超家族中存在大量致癌突变,这些突变是多种癌症背后的驱动力。Ras蛋白介导大量激酶途径,包括MAPK、PI3K和Ral途径。由于直到最近Ras都被认为是不可成药的,因此人们尝试对Ras下游途径进行药物靶向治疗,取得了不同程度的成功,不过耐药性常常是个问题。人们认为,在各种Ras突变体存在的情况下激酶途径激活之间的细微差别导致了耐药性,然而,在不同的Ras突变背景下激活不同途径的背后原因尚未完全阐明。事实上,这种差异往往取决于癌症类型和疾病进展。然而,我们正处于Ras突变体靶向治疗的革命时代,直接靶向KRAS-G12C的抑制剂给该领域带来了变革,并在近年来获得了美国食品药品监督管理局(FDA)的批准。然而,这些药物只对一部分患者有益。大约90%的Ras突变癌症不是KRAS-G12C突变,因此就产生了一个问题,即Ras内其他不同的氨基酸取代是否有一天也能以类似的方式成为可靶向的目标,以及更好地理解这些各种突变体激活的下游途径是否真的能进一步改善治疗。在这里,我们讨论了在一系列Ras突变致癌背景下激酶途径的偏好,并评估了针对各种Ras突变体的药物靶向治疗的最新进展。最终,我们将研究针对Ras介导的癌症的个体化药物治疗方法的实用性。