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肿瘤中的髓源性抑制细胞:当前认识与未来展望

英文原题:Myeloid-derived suppressor cells in cancer: Current knowledge and future perspectives.

查看英文原题

Myeloid-derived suppressor cells in cancer: Current knowledge and future perspectives.

PubMed 2024/09/05(内容时间) Int Immunopharmacol Q1 · IF 5.6(JCR 2025)

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中文摘要

MDSC(髓系来源抑制细胞)对癌症免疫系统逃逸至关重要。它们在 peripheral blood 和肿瘤微环境中积累,抑制 T 细胞、NK 细胞和树突状细胞等免疫细胞。它们通过分泌细胞因子和生长因子促进肿瘤血管生成和转移,并促成促肿瘤环境。癌症患者中 MDSC 的积累与不良预后和对多种癌症治疗的耐药性有关。靶向 MDSC 及其免疫抑制机制可能通过开发抑制 MDSC 功能、阻止其积累和破坏促肿瘤环境的药物来改善治疗结果并增强免疫监视。本综述详细概述了癌症中 MDSC 研究及其发育和功能的调控。详细讨论了 MDSC 作为不同类型癌症中预后和预测生物标志物的相关性,以及靶向 MDSC 的治疗方法的最新进展。

展开英文摘要原文

MDSCs (myeloid-derived suppressor cells) are crucial for immune system evasion in cancer. They accumulate in peripheral blood and tumor microenvironment, suppressing immune cells like T-cells, natural killer cells and dendritic cells. They promote tumor angiogenesis and metastasis by secreting cytokines and growth factors and contribute to a tumor-promoting environment. The accumulation of MDSCs in cancer patients has been linked to poor prognosis and resistance to various cancer therapies.

Targeting MDSCs and their immunosuppressive mechanisms may improve treatment outcomes and enhance immune surveillance by developing drugs that inhibit MDSC function, by preventing their accumulation and by disrupting the tumor-promoting environment.

This review presents a detailed overview of the MDSC research in cancer with regulation of their development and function. The relevance of MDSC as a prognostic and predictive biomarker in different types of cancers, along with recent advancements on the therapeutic approaches to target MDSCs are discussed in detail.

论文信息

作者
Rajkumari S、Singh J、Agrawal U、Agrawal S
第一作者单位
ICMR National Institute of Medical Statistics, Ansari Nagar, New Delhi 110029, India.India
通讯作者单位
Discovery Research Division, Indian Council of Medical Research, Ansari Nagar, New Delhi 110029, India. Electronic address: drsandeepagrawal25@gmail.com.India
文献类型
综述
期刊
International immunopharmacology2024 Dec 5
原文标识
PubMed 39236460 · DOI 10.1016/j.intimp.2024.112949