Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Cancer Cell. 2022 Sep 12;40(9):908-910. doi: 10.1016/j.ccell.2022.08.018.
Covalent inhibitors of oncogenic KRAS have demonstrated impressive clinical responses; however, therapeutic resistance has been commonly observed. In this issue, Zhang and colleagues demonstrate that small molecule KRAS inhibitors can generate haptenated major histocompatibility complex (MHC) class I:peptide complexes, which represent attractive targets for immune-based therapies to combat pharmacologic resistance.
致癌 KRAS 的共价抑制剂已显示出令人印象深刻的临床反应;然而,治疗耐药性已被普遍观察到。在本期杂志中,Zhang 及其同事表明,小分子 KRAS 抑制剂可以产生半抗原化主要组织相容性复合物 (MHC) Ⅰ类:肽复合物,这代表了一种有吸引力的免疫治疗靶点,以对抗药物耐药性。