Wu Cheng Pei, Vaishnavi Aria
Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Thoracic Head & Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer Res. 2025 Sep 2;85(17):3186-3188. doi: 10.1158/0008-5472.CAN-25-1989.
Lung adenocarcinoma has become a paradigm for precision oncology and success with targeted therapies. However, large chunks of the pie chart of molecular drivers remain unknown, preventing many patients from similarly benefiting from this strategy. Here, we highlight the side-by-side release of two impactful studies from Mozzarelli and colleagues and DiMarco and colleagues in this issue of Cancer Research. Here, each team generated unique mouse models characterizing a novel and potentially actionable driver and facilitator of acquired drug resistance in lung adenocarcinoma, RIT1M90I. Both study teams describe and characterize their new mouse models, reporting the tumor latency and importantly revealing the sensitivity of RIT1-mutant lung tumors to SHP2 or RAS tricomplex inhibitors. Collectively, these findings highlight the importance of RIT1M90I as an actionable driver of lung adenocarcinoma and a potent mediator of acquired drug resistance. These new RIT1-driven lung cancer models represent valuable tools for the preclinical testing and translation of different therapeutic strategies for this patient population. See related article by Mozzarelli et al., p. 3196 See related article by DiMarco et al., p. 3207.
肺腺癌已成为精准肿瘤学及靶向治疗成功的典范。然而,分子驱动因素的饼状图中仍有很大一部分未知,这使得许多患者无法同样从这一策略中获益。在此,我们重点介绍本期《癌症研究》中莫扎雷利及其同事和迪马尔科及其同事发表的两项具有影响力的研究。在这两项研究中,每个团队都构建了独特的小鼠模型,用以表征肺腺癌中一种新的、可能具有可操作性的获得性耐药驱动因素和促进因素——RIT1M90I。两个研究团队都描述并表征了各自的新小鼠模型,报告了肿瘤潜伏期,并且重要的是揭示了RIT1突变型肺肿瘤对SHP2或RAS三聚体抑制剂的敏感性。总体而言,这些发现凸显了RIT1M90I作为肺腺癌可操作驱动因素和获得性耐药有效介导因素的重要性。这些新的由RIT1驱动的肺癌模型是针对该患者群体进行不同治疗策略临床前测试和转化的宝贵工具。见莫扎雷利等人的相关文章,第3196页。见迪马尔科等人的相关文章,第3207页。