O'Keefe Sophie, Wang Qiwei
Department of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia, USA.
University of Virginia Comprehensive Cancer Center, Charlottesville, Virginia, USA.
J Clin Invest. 2025 Apr 1;135(7):e191094. doi: 10.1172/JCI191094.
Non-small cell lung cancer (NSCLC), the most common type of lung cancer, remains a leading cause of cancer-related mortality worldwide. Immune checkpoint inhibitors (ICIs) have emerged as a promising therapy for NSCLC but only benefit a subset of patients. In this issue of the JCI, Jiao et al. revealed that acetyl-CoA acetyltransferase 1 (ACAT1) limited the efficacy of ICIs in NSCLC by impeding tertiary lymphoid structures (TLS) in the tumor microenvironment (TME). Targeting ACAT1 in tumor cells reduced mitochondrial hypersuccinylation and oxidative stress, enhancing TLS abundance and improving the efficacy of ICIs in preclinical murine models of NSCLC.
非小细胞肺癌(NSCLC)是最常见的肺癌类型,仍然是全球癌症相关死亡的主要原因。免疫检查点抑制剂(ICIs)已成为NSCLC的一种有前景的治疗方法,但仅使一部分患者受益。在本期《临床研究杂志》(JCI)中,焦等人发现乙酰辅酶A乙酰基转移酶1(ACAT1)通过阻碍肿瘤微环境(TME)中的三级淋巴结构(TLS)来限制ICIs在NSCLC中的疗效。在肿瘤细胞中靶向ACAT1可减少线粒体超琥珀酰化和氧化应激,增加TLS丰度,并提高ICIs在NSCLC临床前小鼠模型中的疗效。