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肿瘤免疫治疗新免疫靶点与信号通路的鉴定

英文原题:Identification of new immune target and signaling for cancer immunotherapy.

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Identification of new immune target and signaling for cancer immunotherapy.

PubMed 2025/03/20(内容时间) Cancer Genet Q1 · IF 11(JCR 2025)

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中文摘要

免疫治疗已成为恶性肿瘤的一种创新疗法,通过激活免疫系统识别并清除恶性细胞。肿瘤与免疫系统之间的相互作用日益复杂,因此持续识别新的免疫靶点和信号通路,以制定改进的治疗策略。本文旨在阐明癌症与免疫系统之间的联系,重点关注免疫监视和免疫逃逸机制。综述全面介绍免疫治疗方法,包括免疫检查点抑制剂(CTLA-4、PD-1、PD-L1)、CAR-T 细胞疗法和癌症疫苗,并阐述针对新型免疫检查点 TIM-3、LAG-3 和 TIGIT 的先进疗法。文章还讨论 JAK/STAT、MAPK 和 PI3K-AKT-mTOR 通路与癌症进展及免疫治疗耐药的关系。这些通路失调为发现新的治疗靶点带来希望。综述介绍基因组学、蛋白质组学、免疫肽组学、单细胞质谱、基于 CRISPR 的功能基因组学和生物信息学在免疫靶点识别及癌症相关信号通路绘制中的重要作用。本文还讨论该领域新兴问题,包括肿瘤异质性、免疫相关不良事件(irAE)和个体化治疗,并阐述这些障碍,以促进理解如何通过联合疗法克服障碍、提高免疫治疗疗效。通过拓展对免疫靶点及通路的认识,癌症免疫精准医学有望显著改善患者结局。

展开英文摘要原文

Immunotherapy has become one of the innovative treatments in malignancy as it activates the immune system to find and eliminate malignant cells. The tumor immunology interface has become increasingly intricate, making the identification of new immune targets and signalling pathways on which to base improved therapeutic strategies an ongoing process. This review, we goal to clarify the contacts between cancer and immune system with a focus on immune surveillance as well as immune evasion mechanisms. Comprehensive immunotherapeutic therapies are overviewed with ICI (CTLA-4, PD-1, PD-L1), CAR-T cell therapy, and cancer vaccines whereas, advanced therapies targeting new immune checkpoints are also elucidated including TIM-3, LAG-3, and TIGIT. The JAK/STAT, MAPK and PI3K-AKT-mTOR pathways are reviewed with regards to cancer progression and immunotherapeutic resistance.

The dysregulation of these pathways gives hope for the identification of fresh targets for therapy. Genomics, proteomics, immunopeptidomics, single cell mass spectrometry, CRISPR-based functional genomics and bioinformatics are described as essential for immune target identification and for mapping of cancer relevant signaling pathways.

This review also considers some emerging issues in the subject area like the tumor heterogeneity, immune-related adverse events (irAEs), and personalized treatment. These barriers are described to facilitate the understanding of ways to overcome them and increase the efficacy of immunotherapies through combination therapies. This means that by developing new knowledge of immunological targets and pathways, immunoprecision medicine for cancer could greatly enhance outcomes.

论文信息

作者
Narote S、Desai SA、Patel VP、Deshmukh R、Raut N、Dapse S
第一作者单位
Department of Pharmaceutical Biotechnology, Sanjivani College of Pharmaceutical Education & Research, Savitribai Phule Pune University, Kopargaon, Maharashtra, India.India
通讯作者单位
Department of Pharmaceutical Biotechnology, Sanjivani College of Pharmaceutical Education & Research, Savitribai Phule Pune University, Kopargaon, Maharashtra, India. Electronic address: sharavdesaibpharm@sanjivani.org.in.India
文献类型
综述
期刊
Cancer genetics2025 Jun
原文标识
PubMed 40154216 · DOI 10.1016/j.cancergen.2025.03.004