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乳腺癌细胞衍生的外泌体与巨噬细胞极化与淋巴结转移有关。

Breast cancer cell-derived exosomes and macrophage polarization are associated with lymph node metastasis.

作者信息

Piao Yin Ji, Kim Hoe Suk, Hwang Eun Hye, Woo Jisu, Zhang Meihua, Moon Woo Kyung

机构信息

Department of Radiology, Seoul National University Hospital and Seoul National University College of Medicine, Jongno-Gu, Seoul 03080, Korea.

Department of Biomedical Sciences, Seoul National University College of Medicine, Jongno-Gu, Seoul 03080, Korea.

出版信息

Oncotarget. 2017 Dec 13;9(7):7398-7410. doi: 10.18632/oncotarget.23238. eCollection 2018 Jan 26.

Abstract

Crosstalk between breast cancer and macrophages has potential implications for tumor metastasis. This study investigates macrophage polarization induced by triple-negative breast cancer (TNBC) cell-derived exosomes that promote lymph node (LN) metastasis in orthotopic TNBC models. The MDA-MB-231 cancer cell line expressing the exosomal CD63-red fluorescence (RFP) fusion protein was generated to noninvasively visualize exosome transfer into cancer cells and macrophages. Administration of RFP-tagged exosomes enhanced migration of macrophages and induced macrophage polarization . In orthotopic TNBC models, noninvasive bioluminescent imaging, ultrasound-guided photoacoustic imaging, and histological analysis revealed that intravenous injection of RFP-tagged exosomes promoted primary tumor growth and axillary LN metastasis in which expression of CD206, a marker or alternatively activated type 2 (M2) macrophages, was significantly higher than expression of NOS2, a marker of classically activated type 1 (M1) macrophages. These results suggest breast cancer cell-derived exosomes stimulate macrophage polarization that creates favorable conditions for LN metastatic processes in TNBC.

摘要

乳腺癌与巨噬细胞之间的相互作用对肿瘤转移具有潜在影响。本研究调查了三阴性乳腺癌(TNBC)细胞衍生的外泌体诱导的巨噬细胞极化,这些外泌体在原位TNBC模型中促进淋巴结(LN)转移。构建了表达外泌体CD63-红色荧光蛋白(RFP)融合蛋白的MDA-MB-231癌细胞系,以无创可视化外泌体向癌细胞和巨噬细胞的转移。给予带有RFP标记的外泌体可增强巨噬细胞的迁移并诱导巨噬细胞极化。在原位TNBC模型中,无创生物发光成像、超声引导光声成像和组织学分析显示,静脉注射带有RFP标记的外泌体可促进原发性肿瘤生长和腋窝LN转移,其中2型替代激活巨噬细胞(M2)的标志物CD206的表达显著高于经典激活1型巨噬细胞(M1)的标志物NOS2的表达。这些结果表明,乳腺癌细胞衍生的外泌体刺激巨噬细胞极化,为TNBC的LN转移过程创造了有利条件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a2/5800911/74e803074bbb/oncotarget-09-7398-g001.jpg

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