The miRNA and PD-1/PD-L1 signaling axis: an arsenal of immunotherapeutic targets against lung cancer.

IF 6.1 2区 生物学 Q1 CELL BIOLOGY Cell Death Discovery Pub Date : 2024-09-29 DOI:10.1038/s41420-024-02182-1
Ritu Yadav, Rinku Khatkar, Kenneth C-H Yap, Chloe Yun-Hui Kang, Juncheng Lyu, Rahul Kumar Singh, Surojit Mandal, Adrija Mohanta, Hiu Yan Lam, Elena Okina, Rajiv Ranjan Kumar, Vivek Uttam, Uttam Sharma, Manju Jain, Hridayesh Prakash, Hardeep Singh Tuli, Alan Prem Kumar, Aklank Jain
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Abstract

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.

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miRNA 和 PD-1/PD-L1 信号轴:抗击肺癌的免疫治疗靶点库。
肺癌对一线和二线化疗/放疗具有内在抵抗力,是医疗系统面临的严峻挑战。鉴于肺癌的无菌环境,包括 nivolumab、pembrolizumab、atezolizumab 和 durvalumab 在内的几种免疫治疗药物目前正在全球临床上使用,目的是释放衰竭的 T 细胞反击难治性肿瘤细胞。免疫疗法的反应率有限,并可能导致部分患者出现免疫相关不良事件(irAEs)。因此,深入了解免疫检查点相互作用的调节机制可大大提高肺癌的治疗效果。在这篇综述中,我们探讨了 miRNA 在调节针对肿瘤的免疫原性反应中的作用。我们从各个方面讨论了操纵这些检查点如何使免疫系统对肺癌的反应产生偏差。具体来说,我们研究了改变 miRNA 配置文件如何影响各种免疫检查点抑制剂的活性,重点关注肺癌复杂病变中的 PD-1/PD-L1 通路。我们相信,清楚地了解宿主的 miRNA 图谱可以影响检查点抑制剂的疗效,并为肺癌患者的现有免疫疗法做出重大贡献。此外,我们还讨论了正在进行的免疫治疗药物临床试验,包括作为独立疗法以及与其他疗法联合使用,旨在推动肺癌免疫疗法的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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