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POU1F1 转录因子通过招募和极化巨噬细胞促进乳腺癌转移。

POU1F1 transcription factor promotes breast cancer metastasis via recruitment and polarization of macrophages.

机构信息

Department of Physiology - Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain.

Research Unit, Hospital Fundacion de Jove, Gijón, Spain.

出版信息

J Pathol. 2019 Nov;249(3):381-394. doi: 10.1002/path.5324. Epub 2019 Aug 27.

DOI:10.1002/path.5324
PMID:31292963
Abstract

Cancer progression requires cells surrounding tumors be reeducated and activated to support tumor growth. Oncogenic signals from malignant cells directly influence stromal composition and activation, but the factors mediating this communication are still not well understood. We have previously shown that the transcription factor POU class 1 homeobox 1 (POU1F1), also known as Pit-1, induces profound changes on neoplastic cell-autonomous processes favoring metastasis in human breast cancer. Here we describe for the first time Pit-1-mediated paracrine actions on macrophages in the tumor microenvironment by using cell lines in vitro, zebrafish and mouse models in vivo, and samples from human breast cancer patients. Through the release of CXCL12, Pit-1 in tumor cells was found to mediate the recruitment and polarization of macrophages into tumor-associated macrophages (TAMs). In turn, TAMs collaborated with tumor cells to increase tumor growth, angiogenesis, extravasation and metastasis to lung. Our data reveal a new mechanism of cooperation between tumor cells and macrophages favoring metastasis and poor clinical outcome in human breast cancer, which suggests that Pit-1 and CXCL12 should be further studied as potential prognostic and therapeutic indicators. © 2019 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

摘要

癌症的进展需要肿瘤周围的细胞被重新教育和激活,以支持肿瘤的生长。恶性细胞的致癌信号直接影响基质的组成和激活,但介导这种通讯的因素仍未得到很好的理解。我们之前已经表明,转录因子 POU 类 1 同源框 1(POU1F1),也称为 Pit-1,诱导人类乳腺癌中肿瘤细胞自主过程的深刻变化,有利于转移。在这里,我们首次描述了 Pit-1 通过体外细胞系、斑马鱼和小鼠模型以及来自人类乳腺癌患者的样本对肿瘤微环境中的巨噬细胞的旁分泌作用。通过释放 CXCL12,发现肿瘤细胞中的 Pit-1 介导巨噬细胞募集和极化成为肿瘤相关巨噬细胞(TAMs)。反过来,TAMs 与肿瘤细胞合作增加肿瘤生长、血管生成、渗出和转移到肺部。我们的数据揭示了肿瘤细胞和巨噬细胞之间有利于转移和人类乳腺癌不良临床结局的新合作机制,这表明 Pit-1 和 CXCL12 应进一步作为潜在的预后和治疗指标进行研究。

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