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肿瘤细胞去分化如何驱动免疫逃逸和对免疫治疗的抵抗。

How Tumor Cell Dedifferentiation Drives Immune Evasion and Resistance to Immunotherapy.

机构信息

Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Cancer Res. 2020 Oct 1;80(19):4037-4041. doi: 10.1158/0008-5472.CAN-20-1420. Epub 2020 Jun 18.

DOI:10.1158/0008-5472.CAN-20-1420
PMID:32554552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7541560/
Abstract

Immunotherapy has revolutionized cancer treatment, yet most patients do not respond. While tumor antigens are needed for effective immunotherapy, a favorable tumor immune microenvironment is also critical. In this review, we discuss emerging evidence that tumor cells exploit cellular plasticity and dedifferentiation programs to avoid immune surveillance, which in turn drives metastatic dissemination and resistance to immunotherapy. A deeper understanding of these programs may provide novel opportunities to enhance the efficacy of existing immunotherapies.

摘要

免疫疗法已经彻底改变了癌症治疗方法,但大多数患者没有响应。虽然肿瘤抗原是有效免疫疗法所必需的,但有利的肿瘤免疫微环境也是至关重要的。在这篇综述中,我们讨论了新出现的证据,即肿瘤细胞利用细胞可塑性和去分化程序来逃避免疫监视,这反过来又推动了转移扩散和对免疫疗法的耐药性。对这些程序的更深入了解可能为增强现有免疫疗法的疗效提供新的机会。

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Nat Cancer. 2020 Jan;1(1):28-45. doi: 10.1038/s43018-019-0006-x. Epub 2020 Jan 13.
2
Multimodel preclinical platform predicts clinical response of melanoma to immunotherapy.多模型临床前平台预测黑色素瘤对免疫治疗的临床反应。
Nat Med. 2020 May;26(5):781-791. doi: 10.1038/s41591-020-0818-3. Epub 2020 Apr 13.
3
Cell Intrinsic and Systemic Metabolism in Tumor Immunity and Immunotherapy.肿瘤免疫与免疫治疗中的细胞内在代谢和全身代谢
整合素β1/踝蛋白1机械激活通过泛素依赖性细胞周期蛋白依赖性激酶1α降解增强口腔鳞状细胞癌中CD44的特征干性。
Oncogene. 2025 Jun;44(20):1530-1544. doi: 10.1038/s41388-025-03317-z. Epub 2025 Mar 5.
4
Exploring thymic stromal lymphopoietin in the breast cancer microenvironment: A preliminary study.探索乳腺癌微环境中的胸腺基质淋巴细胞生成素:一项初步研究。
Oncol Lett. 2025 Feb 13;29(4):182. doi: 10.3892/ol.2025.14928. eCollection 2025 Apr.
5
Role and value of the tumor microenvironment in the progression and treatment resistance of gastric cancer (Review).肿瘤微环境在胃癌进展和治疗抵抗中的作用和价值(综述)。
Oncol Rep. 2025 Jan;53(1). doi: 10.3892/or.2024.8847. Epub 2024 Nov 29.
6
The molecular features of lung cancer stem cells in dedifferentiation process-driven epigenetic alterations.去分化过程驱动的表观遗传改变中肺癌干细胞的分子特征。
J Biol Chem. 2024 Dec;300(12):107994. doi: 10.1016/j.jbc.2024.107994. Epub 2024 Nov 14.
7
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Front Immunol. 2024 Oct 16;15:1464421. doi: 10.3389/fimmu.2024.1464421. eCollection 2024.
8
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bioRxiv. 2024 Sep 13:2024.09.09.611835. doi: 10.1101/2024.09.09.611835.
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Front Endocrinol (Lausanne). 2024 Jun 6;15:1427723. doi: 10.3389/fendo.2024.1427723. eCollection 2024.
Cancers (Basel). 2020 Apr 1;12(4):852. doi: 10.3390/cancers12040852.
4
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5
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6
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7
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Cancer Discov. 2020 Feb;10(2):270-287. doi: 10.1158/2159-8290.CD-19-0780. Epub 2019 Nov 19.
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Nature. 2019 Nov;575(7781):217-223. doi: 10.1038/s41586-019-1694-1. Epub 2019 Oct 30.
10
The great escape: tumour cell plasticity in resistance to targeted therapy.肿瘤细胞的“大逃亡”:靶向治疗耐药中的可塑性。
Nat Rev Drug Discov. 2020 Jan;19(1):39-56. doi: 10.1038/s41573-019-0044-1. Epub 2019 Oct 10.