Department of Surgery, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
Department of General Surgery, Hepatopancreatobiliary-Unit, School of Medicine, Kerem Aydınlar Campus at Acıbadem University, Istanbul, Turkey.
JCI Insight. 2022 Jan 11;7(1):e153688. doi: 10.1172/jci.insight.153688.
KRAS mutations are the drivers of various cancers, including non-small cell lung cancer, colon cancer, and pancreatic cancer. Over the last 30 years, immense efforts have been made to inhibit KRAS mutants and oncogenic KRAS signaling using inhibitors. Recently, specific targeting of KRAS mutants with small molecules revived the hopes for successful therapies for lung, pancreatic, and colorectal cancer patients. Moreover, advances in gene editing, protein engineering, and drug delivery formulations have revolutionized cancer therapy regimens. New therapies aim to improve immune surveillance and enhance antitumor immunity by precisely targeting cancer cells harboring oncogenic KRAS. Here, we review recent KRAS-targeting strategies, their therapeutic potential, and remaining challenges to overcome. We also highlight the potential synergistic effects of various combinatorial therapies in preclinical and clinical trials.
KRAS 突变是包括非小细胞肺癌、结肠癌和胰腺癌在内的多种癌症的驱动因素。在过去的 30 年中,人们付出了巨大的努力,使用抑制剂来抑制 KRAS 突变体和致癌 KRAS 信号。最近,使用小分子特异性靶向 KRAS 突变体重新燃起了为肺癌、胰腺癌和结直肠癌患者成功治疗的希望。此外,基因编辑、蛋白质工程和药物递送配方的进步彻底改变了癌症治疗方案。新的治疗方法旨在通过精确靶向携带致癌 KRAS 的癌细胞来改善免疫监测并增强抗肿瘤免疫。在这里,我们回顾了最近的 KRAS 靶向策略、它们的治疗潜力以及克服这些策略仍需解决的挑战。我们还强调了各种组合疗法在临床前和临床试验中的潜在协同作用。