Characteristics of tumor microenvironment and novel immunotherapeutic strategies for non-small cell lung cancer

IF 7.6 Q1 ONCOLOGY
Fen Wang , Mingyi Yang , Weichi Luo , Qing Zhou
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引用次数: 3

Abstract

Immune checkpoint inhibitor-based immunotherapy has revolutionized the treatment approach of non-small cell lung cancer (NSCLC). Monoclonal antibodies against programmed cell death-1 (PD-1) and PD-ligand 1 (PD-L1) are widely used in clinical practice, but other antibodies that can circumvent innate and acquired resistance are bound to undergo preclinical and clinical studies. However, tumor cells can develop and facilitate the tolerogenic nature of the tumor microenvironment (TME), resulting in tumor progression. Therefore, the immune escape mechanisms exploited by growing lung cancer involve a fine interplay between all actors in the TME. A better understanding of the molecular biology of lung cancer and the cellular/molecular mechanisms involved in the crosstalk between lung cancer cells and immune cells in the TME could identify novel therapeutic weapons in the old war against lung cancer. This article discusses the role of TME in the progression of lung cancer and pinpoints possible advances and challenges of immunotherapy for NSCLC.

癌症肿瘤微环境特征及新的免疫治疗策略
基于免疫检查点抑制剂的免疫疗法已经彻底改变了非小细胞肺癌(NSCLC)的治疗方法。抗程序性细胞死亡-1 (PD-1)和pd -配体-1 (PD-L1)的单克隆抗体广泛应用于临床实践,但其他能够规避先天和获得性耐药的抗体势必要进行临床前和临床研究。然而,肿瘤细胞可以发展并促进肿瘤微环境(TME)的耐受性,导致肿瘤进展。因此,生长中的肺癌利用的免疫逃逸机制涉及TME中所有参与者之间的良好相互作用。更好地了解肺癌的分子生物学以及肺癌细胞与免疫细胞在TME中相互作用的细胞/分子机制,可以在对抗肺癌的古老战争中找到新的治疗武器。本文讨论了TME在肺癌进展中的作用,并指出了非小细胞肺癌免疫治疗的可能进展和挑战。
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
CiteScore
14.20
自引率
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