Secretome derived from breast tumor cell lines alters the morphology of human umbilical vein endothelial cells

Q3 Biochemistry, Genetics and Molecular Biology
E. O. Gómez, Y. Chirino, N. Delgado-Buenrostro, Alejandro López-Saavedra, N. Meraz-Cruz, R. López-Marure
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引用次数: 3

Abstract

Abstract Metastases, responsible for most of the solid tumor associated deaths, require angiogenesis and changes in endothelial cells. In this work, the effect of the secretomes of three breast tumor cell lines (MCF-7, MDA-MB-231 and ZR-75-30) on human umbilical vein endothelial cells (HUVEC) morphology was investigated. HUVEC treated with secretomes from breast cells were analyzed by confocal and time-lapse microscopy. Secretomes from ZR-75-30 and MDA-MB-231 cells modify the morphology and adhesion of HUVEC. These changes may provoke the loss of endothelial monolayer integrity. In consequence, tumor cells could have an increased access to circulation, which would then enhance metastasis.
来源于乳腺肿瘤细胞系的分泌组改变了人脐静脉内皮细胞的形态
转移性肿瘤是大多数实体瘤相关死亡的原因,它需要血管生成和内皮细胞的改变。本文研究了乳腺肿瘤细胞系MCF-7、MDA-MB-231和ZR-75-30分泌组对人脐静脉内皮细胞(HUVEC)形态的影响。用乳腺细胞分泌组处理HUVEC,用共聚焦显微镜和延时显微镜分析。ZR-75-30和MDA-MB-231细胞分泌组改变HUVEC的形态和粘附。这些变化可能引起内皮单层完整性的丧失。因此,肿瘤细胞进入血液循环的途径会增加,从而促进转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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