下一代肿瘤不可知靶点即将出现
Next-generation tumor-agnostic targets on the horizon.
肿瘤不可知药物开发将肿瘤学重新聚焦于共享的分子依赖性而非组织来源,从而能够针对跨肿瘤的罕见可操作驱动因素进行高效开发。
英文原题:KRAS Inhibitors- yes but what next? Direct targeting of KRAS- vaccines, adoptive T cell therapy and beyond.
Kirsten大鼠肉瘤病毒癌基因同源物(KRAS)是RAS-MAPK通路的原癌基因。
Kirsten大鼠肉瘤病毒癌基因同源物(KRAS)是RAS-MAPK通路的原癌基因。KRAS突变存在于多种恶性肿瘤中,包括肺癌、结直肠癌和胰腺癌。在KRAS G12C抑制剂sotorasib近期获批之前,KRAS缺乏靶向治疗导致携带KRAS突变肿瘤的患者预后较差。虽然sotorasib的条件性批准对携带KRAS G12C突变的患者而言是一项重大突破,但G12C仅占KRAS突变患者的一小部分,且对G12C抑制剂的最终耐药不可避免。这篇关于KRAS抑制剂的综合性综述涵盖了不断积累的证据,不仅涉及G12C抑制剂,还涉及其他针对KRAS的治疗尝试,包括联合治疗以及疫苗、过继性T细胞疗法、蛋白水解靶向嵌合体(PROTAC)和CRISPR/Cas9的直接抑制。
Kirsten rat sarcoma viral oncogene homolog (KRAS) is a proto-oncogene of the RAS-MAPK pathway. KRAS mutations are present in a variety of malignancies including lung, colorectal, and pancreatic cancer. Until the recent approval of sotorasib, a KRAS G12C inhibitor, lack of targeted therapy for KRAS has resulted in poor prognosis of patients with tumors harboring KRAS mutations. While the conditional approval of sotorasib was a major breakthrough for those patients harboring KRAS G12C mutations, G12C only accounts for a fraction of those with KRAS mutations and eventual resistance to G12C inhibitors are unavoidable. This comprehensive review on KRAS inhibitors covers accumulating evidence on not only the G12C inhibitors but also other therapeutic attempts to tackle KRAS including combination therapy as well as direct inhibition with vaccines, adoptive T cell therapy, proteolysis-targeted chimeras (PROTACs) and CRISPR/Cas9.
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