Karachaliou Anastasia, Kotteas Elias, Fiste Oraianthi, Syrigos Konstantinos
Oncology Unit, Third Department of Internal Medicine and Laboratory, Medical School, National and Kapodistrian University of Athens, "Sotiria" General Hospital, 11527 Athens, Greece.
Cancers (Basel). 2024 Apr 9;16(8):1447. doi: 10.3390/cancers16081447.
Kirsten rat sarcoma virus (KRAS) is the most frequently found oncogene in human cancers, including non-small-cell lung cancer (NSCLC). For many years, KRAS was considered "undruggable" due to its structure and difficult targeting. However, the discovery of the switch II region in the KRAS-G12C-mutated protein has changed the therapeutic landscape with the design and development of novel direct KRAS-G12C inhibitors. Sotorasib and adagrasib are FDA-approved targeted agents for pre-treated patients with KRAS-G12C-mutated NSCLC. Despite promising results, the efficacy of these novel inhibitors is limited by mechanisms of resistance. Ongoing studies are evaluating combination strategies for overcoming resistance. In this review, we summarize the biology of the KRAS protein and the characteristics of KRAS mutations. We then present current and emerging therapeutic approaches for targeting KRAS mutation subtypes intending to provide individualized treatment for lung cancer harboring this challenging driver mutation.
Kirsten 大鼠肉瘤病毒(KRAS)是人类癌症中最常见的致癌基因,包括非小细胞肺癌(NSCLC)。多年来,由于其结构和难以靶向,KRAS 被认为是“不可成药的”。然而,KRAS-G12C 突变蛋白中开关 II 区域的发现,随着新型直接 KRAS-G12C 抑制剂的设计和开发,改变了治疗格局。索托拉西布和阿达格拉西布是美国食品药品监督管理局(FDA)批准用于治疗 KRAS-G12C 突变 NSCLC 患者的靶向药物。尽管取得了令人鼓舞的结果,但这些新型抑制剂的疗效受到耐药机制的限制。正在进行的研究正在评估克服耐药性的联合策略。在这篇综述中,我们总结了 KRAS 蛋白的生物学特性和 KRAS 突变的特征。然后,我们介绍了针对 KRAS 突变亚型的当前和新兴治疗方法,旨在为携带这种具有挑战性的驱动突变的肺癌患者提供个体化治疗。