Oh Michael S, Abascal Jensen, Rennels Austin K, Salehi-Rad Ramin, Dubinett Steven M, Liu Bin
Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
Department of Medicine, VA Greater Los Angeles Healthcare System, Los Angeles, CA 90073, USA.
Cancers (Basel). 2025 Mar 19;17(6):1027. doi: 10.3390/cancers17061027.
Resistance to immune checkpoint inhibitors (ICIs) represents a major challenge for the effective treatment of non-small cell lung cancer (NSCLC). Tumor heterogeneity has been identified as an important mechanism of treatment resistance in cancer and has been increasingly implicated in ICI resistance. The diversity and clonality of tumor neoantigens, which represent the target epitopes for tumor-specific immune cells, have been shown to impact the efficacy of immunotherapy. Advances in genomic techniques have further enhanced our understanding of clonal landscapes within NSCLC and their evolution in response to therapy. In this review, we examine the role of tumor heterogeneity during immune surveillance in NSCLC and highlight its spatial and temporal evolution as revealed by modern technologies. We explore additional sources of heterogeneity, including epigenetic and metabolic factors, that have come under greater scrutiny as potential mediators of the immune response. We finally discuss the implications of tumor heterogeneity on the efficacy of ICIs and highlight potential strategies for overcoming therapeutic resistance.
对免疫检查点抑制剂(ICI)产生耐药性是有效治疗非小细胞肺癌(NSCLC)的一项重大挑战。肿瘤异质性已被确认为癌症治疗耐药的重要机制,并且越来越多地与ICI耐药相关。肿瘤新抗原的多样性和克隆性代表了肿瘤特异性免疫细胞的靶表位,已被证明会影响免疫治疗的疗效。基因组技术的进步进一步加深了我们对NSCLC内克隆格局及其对治疗反应演变的理解。在本综述中,我们研究了肿瘤异质性在NSCLC免疫监视过程中的作用,并强调了现代技术所揭示的其空间和时间演变。我们探讨了异质性的其他来源,包括表观遗传和代谢因素,这些因素作为免疫反应的潜在介质受到了更多的审视。我们最后讨论了肿瘤异质性对ICI疗效的影响,并强调了克服治疗耐药性的潜在策略。