Yadav Ritu, Khatkar Rinku, Yap Kenneth C-H, Kang Chloe Yun-Hui, Lyu Juncheng, Singh Rahul Kumar, Mandal Surojit, Mohanta Adrija, Lam Hiu Yan, Okina Elena, Kumar Rajiv Ranjan, Uttam Vivek, Sharma Uttam, Jain Manju, Prakash Hridayesh, Tuli Hardeep Singh, Kumar Alan Prem, Jain Aklank
Non-Coding RNA and Cancer Biology Laboratory, Department of Zoology, Central University of Punjab, Bathinda, Punjab, India.
Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Cell Death Discov. 2024 Sep 29;10(1):414. doi: 10.1038/s41420-024-02182-1.
Lung cancer is a severe challenge to the health care system with intrinsic resistance to first and second-line chemo/radiotherapies. In view of the sterile environment of lung cancer, several immunotherapeutic drugs including nivolumab, pembrolizumab, atezolizumab, and durvalumab are currently being used in clinics globally with the intention of releasing exhausted T-cells back against refractory tumor cells. Immunotherapies have a limited response rate and may cause immune-related adverse events (irAEs) in some patients. Hence, a deeper understanding of regulating immune checkpoint interactions could significantly enhance lung cancer treatments. In this review, we explore the role of miRNAs in modulating immunogenic responses against tumors. We discuss various aspects of how manipulating these checkpoints can bias the immune system's response against lung cancer. Specifically, we examine how altering the miRNA profile can impact the activity of various immune checkpoint inhibitors, focusing on the PD-1/PD-L1 pathway within the complex landscape of lung cancer. We believe that a clear understanding of the host's miRNA profile can influence the efficacy of checkpoint inhibitors and significantly contribute to existing immunotherapies for lung cancer patients. Additionally, we discuss ongoing clinical trials involving immunotherapeutic drugs, both as standalone treatments and in combination with other therapies, intending to advance the development of immunotherapy for lung cancer.
肺癌对医疗保健系统构成严峻挑战,其对一线和二线化疗/放疗具有内在抗性。鉴于肺癌的无菌环境,包括纳武单抗、帕博利珠单抗、阿特珠单抗和度伐利尤单抗在内的几种免疫治疗药物目前正在全球范围内的临床中使用,目的是使耗竭的T细胞重新对抗难治性肿瘤细胞。免疫疗法的有效率有限,并且在一些患者中可能会引起免疫相关不良事件(irAE)。因此,更深入地了解调节免疫检查点相互作用可显著增强肺癌治疗效果。在本综述中,我们探讨了微小RNA(miRNA)在调节针对肿瘤的免疫原性反应中的作用。我们讨论了操纵这些检查点如何影响免疫系统对肺癌反应的各个方面。具体而言,我们研究了改变miRNA谱如何影响各种免疫检查点抑制剂的活性,重点关注肺癌复杂格局中的程序性死亡受体1(PD-1)/程序性死亡配体1(PD-L1)途径。我们认为,清楚了解宿主的miRNA谱可影响检查点抑制剂的疗效,并对现有的肺癌患者免疫治疗做出重大贡献。此外,我们讨论了正在进行的涉及免疫治疗药物的临床试验,这些药物既作为单一疗法,也与其他疗法联合使用,旨在推动肺癌免疫治疗的发展。