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衰老与癌症交汇点上的髓源性抑制细胞(MDSCs)

Myeloid-Derived Suppressor Cells (MDSCs) at the Crossroad of Senescence and Cancer.

作者信息

Talarico Giovanna, Orecchioni Stefania, Falvo Paolo, Bertolini Francesco

机构信息

Laboratory of Hematology-Oncology, European Institute of Oncology IRCCS, Via Ripamonti 435, 20141 Milan, Italy.

Onco-Tech Lab, European Institute of Oncology IRCCS and Politecnico di Milano, 20141 Milan, Italy.

出版信息

Cancers (Basel). 2025 Jul 4;17(13):2251. doi: 10.3390/cancers17132251.

DOI:10.3390/cancers17132251
PMID:40647547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12248894/
Abstract

The family of myeloid-derived suppressor cells (MDSCs) includes a heterogeneous group of partially immature cells belonging to the myeloid lineage with potent immunosuppressive functions. They might be increased in the peripheral blood of cancer patients and in the microenvironment of cancer lesions, where they act in suppressing adaptive and innate immune cells, promoting tumor progression, and facilitating resistance to therapy. Several-albeit still limited-studies have shown higher levels of MDSCs in elderly cancer patients, correlating with poorer outcomes and a reduced response to immunotherapies. Thus, MDSCs may serve as biomarkers for prognosis or therapy response in this population, and MDSC-targeting therapies aimed at reducing their number or function may enhance the effectiveness of immunotherapies in older adults. Additionally, a better understanding of MDSCs may help to overcome some age-related barriers in cancer treatments.

摘要

髓源性抑制细胞(MDSC)家族包括一群异质性的部分未成熟细胞,它们属于具有强大免疫抑制功能的髓系谱系。在癌症患者的外周血和癌症病灶的微环境中,它们的数量可能会增加,在这些地方它们发挥作用抑制适应性免疫细胞和固有免疫细胞,促进肿瘤进展,并促进对治疗的抵抗。一些研究(尽管仍然有限)表明老年癌症患者体内的MDSC水平较高,这与较差的预后和对免疫疗法的反应降低相关。因此,MDSC可能作为该人群预后或治疗反应的生物标志物,旨在减少其数量或功能的靶向MDSC疗法可能会提高免疫疗法在老年人中的有效性。此外,更好地了解MDSC可能有助于克服癌症治疗中一些与年龄相关的障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ec/12248894/30d4868aad46/cancers-17-02251-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ec/12248894/9c696e7a0542/cancers-17-02251-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ec/12248894/30d4868aad46/cancers-17-02251-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ec/12248894/9c696e7a0542/cancers-17-02251-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ec/12248894/30d4868aad46/cancers-17-02251-g002.jpg

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本文引用的文献

1
MDSC checkpoint blockade therapy: a new breakthrough point overcoming immunosuppression in cancer immunotherapy.髓源性抑制细胞(MDSC)检查点阻断疗法:癌症免疫治疗中克服免疫抑制的新突破点。
Cancer Gene Ther. 2025 Apr;32(4):371-392. doi: 10.1038/s41417-025-00886-9. Epub 2025 Mar 26.
2
Metabolic regulation of myeloid-derived suppressor cells in tumor immune microenvironment: targets and therapeutic strategies.肿瘤免疫微环境中髓源性抑制细胞的代谢调控:靶点与治疗策略
Theranostics. 2025 Jan 13;15(6):2159-2184. doi: 10.7150/thno.105276. eCollection 2025.
3
Age-dependent differences in breast tumor microenvironment: challenges and opportunities for efficacy studies in preclinical models.
乳腺肿瘤微环境中的年龄依赖性差异:临床前模型疗效研究的挑战与机遇
Cell Death Differ. 2025 Jan 27. doi: 10.1038/s41418-025-01447-1.
4
NF-κB pathway and angiogenesis: insights into colorectal cancer development and therapeutic targets.核因子-κB通路与血管生成:对结直肠癌发展及治疗靶点的见解
Eur J Med Res. 2024 Dec 19;29(1):610. doi: 10.1186/s40001-024-02168-w.
5
Emerging insights into epigenetics and hematopoietic stem cell trafficking in age-related hematological malignancies.衰老相关血液系统恶性肿瘤中表观遗传学和造血干细胞归巢的新认识。
Stem Cell Res Ther. 2024 Nov 6;15(1):401. doi: 10.1186/s13287-024-04008-4.
6
Increased circulating polymorphonuclear myeloid-derived suppressor cells are associated with prognosis of metastatic castration-resistant prostate cancer.循环中增多的多形核髓系来源的抑制性细胞与转移性去势抵抗性前列腺癌的预后相关。
Front Immunol. 2024 Jun 3;15:1372771. doi: 10.3389/fimmu.2024.1372771. eCollection 2024.
7
Hyperexpression of tumor necrosis factor receptor 2 inhibits differentiation of myeloid-derived suppressor cells by instigating apolarity during ageing.肿瘤坏死因子受体2的过表达通过在衰老过程中引发极性异常来抑制髓源性抑制细胞的分化。
MedComm (2020). 2024 Jun 12;5(6):e605. doi: 10.1002/mco2.605. eCollection 2024 Jun.
8
The aged tumor microenvironment limits T cell control of cancer.衰老的肿瘤微环境限制了 T 细胞对癌症的控制。
Nat Immunol. 2024 Jun;25(6):1033-1045. doi: 10.1038/s41590-024-01828-7. Epub 2024 May 14.
9
Myeloid-derived suppressor cells from tumour-bearing mice induce the population expansion of CD19FcγRIIb regulatory B cells via PD-L1.荷瘤小鼠的髓源性抑制细胞通过程序性死亡配体1诱导CD19FcγRIIb调节性B细胞的群体扩增。
Immunology. 2024 May;172(1):127-143. doi: 10.1111/imm.13763. Epub 2024 Feb 8.
10
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Front Immunol. 2023 Oct 18;14:1258291. doi: 10.3389/fimmu.2023.1258291. eCollection 2023.