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巨噬细胞亚型在培养中抑制乳腺癌增殖。

Macrophage subtypes inhibit breast cancer proliferation in culture.

作者信息

Varady Sophia R S, Greiner Daniel, Roh-Johnson Minna

机构信息

Department of Biochemistry, University of Utah School of Medicine; Salt Lake City, UT 84112.

出版信息

Mol Biol Cell. 2025 Jan 1;36(1):br2. doi: 10.1091/mbc.E24-06-0241. Epub 2024 Nov 27.

DOI:10.1091/mbc.E24-06-0241
PMID:39602294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11742110/
Abstract

Macrophages are a highly plastic cell type that adopt distinct subtypes and functional states depending on environmental cues. These functional states can vary widely, with distinct macrophages capable of displaying opposing functions. We sought to understand how macrophage subtypes that exist on two ends of a spectrum influence the function of other cells. We used a coculture system with primary human macrophages to probe the effects of macrophage subtypes on breast cancer cell proliferation. Our studies revealed a surprising phenotype in which both macrophage subtypes inhibited cancer cell proliferation compared with cancer cells alone. Of particular interest, using two different proliferation assays with two different breast cancer cell lines, we showed that differentiating macrophages into a "protumor" subtype inhibited breast cancer cell proliferation. These findings are inconsistent with the prevailing interpretation that "protumor" macrophages promote cancer cell proliferation and suggest a re-evaluation of how these interpretations are made.

摘要

巨噬细胞是一种高度可塑性的细胞类型,根据环境线索可呈现不同的亚型和功能状态。这些功能状态差异很大,不同的巨噬细胞能够表现出相反的功能。我们试图了解处于谱系两端的巨噬细胞亚型如何影响其他细胞的功能。我们使用原代人巨噬细胞共培养系统来探究巨噬细胞亚型对乳腺癌细胞增殖的影响。我们的研究揭示了一种令人惊讶的表型,与单独的癌细胞相比,两种巨噬细胞亚型均抑制癌细胞增殖。特别有趣的是,使用两种不同的增殖测定方法和两种不同的乳腺癌细胞系,我们发现将巨噬细胞分化为“促肿瘤”亚型会抑制乳腺癌细胞增殖。这些发现与“促肿瘤”巨噬细胞促进癌细胞增殖的主流观点不一致,并提示对这些观点的形成方式进行重新评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/e52643b3dffc/mbc-36-br2-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/4bd51a51e183/mbc-36-br2-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/79f1fa8a2ec1/mbc-36-br2-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/e2d426774da6/mbc-36-br2-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/00a1b53dfccc/mbc-36-br2-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/e52643b3dffc/mbc-36-br2-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/4bd51a51e183/mbc-36-br2-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/79f1fa8a2ec1/mbc-36-br2-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/e2d426774da6/mbc-36-br2-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/00a1b53dfccc/mbc-36-br2-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c481/11742110/e52643b3dffc/mbc-36-br2-g005.jpg

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LINC00330/CCL2 axis-mediated ESCC TAM reprogramming affects tumor progression.LINC00330/CCL2 轴介导的 ESCC TAM 重编程影响肿瘤进展。
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Molecules. 2024 Mar 26;29(7):1469. doi: 10.3390/molecules29071469.
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Biomed Pharmacother. 2024 Mar;172:116269. doi: 10.1016/j.biopha.2024.116269. Epub 2024 Feb 16.
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Calcitriol promotes M2 polarization of tumor-associated macrophages in 4T1 mouse mammary gland cancer via the induction of proinflammatory cytokines.骨化三醇通过诱导促炎细胞因子促进 4T1 小鼠乳腺癌中肿瘤相关巨噬细胞向 M2 极化。
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Astragaloside IV antagonizes the malignant progression of breast cancer induced by macrophage M2 polarization through the TGF-β-regulated Akt/Foxo1 pathway.黄芪甲苷通过 TGF-β 调节的 Akt/Foxo1 通路拮抗巨噬细胞 M2 极化诱导的乳腺癌恶性进展。
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Garcinone E suppresses breast cancer growth and metastasis by modulating tumor-associated macrophages polarization via STAT6 signaling. Garcinone E 通过调节 STAT6 信号抑制肿瘤相关巨噬细胞极化从而抑制乳腺癌的生长和转移。
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