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天然产物对肿瘤微环境中髓源性抑制细胞的调控作用。

Modulation of Myeloid-Derived Suppressor Cells in the Tumor Microenvironment by Natural Products.

机构信息

Grupo de Inmunobiología y Biología Celular, Facultad de Ciencias, Pontificia Universidad Javeriana, Bogotá, Colombia.

Departamento de Microbiología, Pontificia Universidad Javeriana, Carrera 7 # 43-82. Edificio 50 Laboratorio 101, Bogotá, Colombia.

出版信息

Arch Immunol Ther Exp (Warsz). 2023 Jul 6;71(1):17. doi: 10.1007/s00005-023-00681-0.

DOI:10.1007/s00005-023-00681-0
PMID:37410164
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10326112/
Abstract

During carcinogenesis, the microenvironment plays a fundamental role in tumor progression and resistance. This tumor microenvironment (TME) is characterized by being highly immunosuppressive in most cases, which makes it an important target for the development of new therapies. One of the most important groups of cells that orchestrate immunosuppression in TME is myeloid-derived suppressor cells (MDSCs), which have multiple mechanisms to suppress the immune response mediated by T lymphocytes and thus protect the tumor. In this review, we will discuss the importance of modulating MDSCs as a therapeutic target and how the use of natural products, due to their multiple mechanisms of action, can be a key alternative for modulating these cells and thus improve response to therapy in cancer patients.

摘要

在癌症发生过程中,微环境在肿瘤进展和耐药中起着根本性的作用。这种肿瘤微环境(TME)在大多数情况下具有高度免疫抑制性,这使其成为开发新疗法的重要靶点。在 TME 中协调免疫抑制作用的最重要的细胞群之一是髓系来源的抑制细胞(MDSCs),它们具有多种机制来抑制 T 淋巴细胞介导的免疫反应,从而保护肿瘤。在这篇综述中,我们将讨论将 MDSCs 作为治疗靶点的重要性,以及天然产物由于其多种作用机制,如何成为调节这些细胞的关键替代方法,从而改善癌症患者的治疗反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fac/10326112/dbf19be8c52d/5_2023_681_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fac/10326112/15f8e3ceeeca/5_2023_681_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fac/10326112/dbf19be8c52d/5_2023_681_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fac/10326112/15f8e3ceeeca/5_2023_681_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fac/10326112/dbf19be8c52d/5_2023_681_Fig2_HTML.jpg

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Front Immunol. 2022 Nov 10;13:1051998. doi: 10.3389/fimmu.2022.1051998. eCollection 2022.
2
Targeting MDSC Differentiation Using ATRA: A Phase I/II Clinical Trial Combining Pembrolizumab and All-Trans Retinoic Acid for Metastatic Melanoma.用 ATRA 靶向 MDSC 分化:联合派姆单抗和全反式维甲酸治疗转移性黑色素瘤的 I/II 期临床试验。
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3
Extract Decreases the Primary Tumor in a Murine Breast Cancer Model but Not in Melanoma.
移植医学中的免疫调节:细胞治疗应用及未来方向的全面综述
Front Immunol. 2024 Apr 8;15:1372862. doi: 10.3389/fimmu.2024.1372862. eCollection 2024.
提取物可减小小鼠乳腺癌模型中的原发性肿瘤,但对黑色素瘤无效。
Cancers (Basel). 2022 Nov 1;14(21):5383. doi: 10.3390/cancers14215383.
4
Influence of tumor cell-derived TGF-β on macrophage phenotype and macrophage-mediated tumor cell invasion.肿瘤细胞衍生的 TGF-β对巨噬细胞表型和巨噬细胞介导的肿瘤细胞侵袭的影响。
Int J Biochem Cell Biol. 2022 Dec;153:106330. doi: 10.1016/j.biocel.2022.106330. Epub 2022 Nov 4.
5
Myeloid-derived suppressor cells: an emerging target for anticancer immunotherapy.髓系来源的抑制细胞:抗肿瘤免疫治疗的一个新靶点。
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