Tissue factor potentiates adherence of breast cancer cells to human umbilical vein endothelial cells under static and flow conditions.

IF 3.3 3区 生物学 Q3 CELL BIOLOGY Cell Adhesion & Migration Pub Date : 2021-12-01 DOI:10.1080/19336918.2021.1898709
Yanling Jin, Wei Liu, Fengxia Wang, Min Wang, Kai Xu, Aijun Yang, Chenyu Wang, Lihan Zhang, Fangfang Zhang, Min Li
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引用次数: 2

Abstract

Tissue factor (TF) has been extensively studied for tumor metastasis, but its role in mediating cancer cell adhesion to vasculature remains unknown. This study aimed to measure the ability of TF to mediate the adhesion of breast cancer cells to human umbilical vein endothelial cells (HUVECs). MDA-MB-231 cells expressed the highest TF level and adhered more to HUVECs under static and flow conditions, a neutralizing TF antibody abolished the enhanced adhesion of MDA-MB-231 cells to HUVECs. Recombinant human soluble TF (rTF) bonded β1integrin on HUVECs surfaces, β1 or α3integrin antibody combined with TF antibody abolished more cell-cell adhesion. These data suggested that TF mediated adhesion of breast cancer cells to endothelial cells may rely on β1integrin on HUVECs surfaces.

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组织因子增强了乳腺癌细胞在静态和流动条件下对人脐静脉内皮细胞的粘附。
组织因子(TF)在肿瘤转移中的作用已被广泛研究,但其在介导癌细胞粘附血管中的作用尚不清楚。本研究旨在检测TF介导乳腺癌细胞与人脐静脉内皮细胞(HUVECs)粘附的能力。在静态和流动条件下,MDA-MB-231细胞表达的TF水平最高,对HUVECs的粘附更强,中和性TF抗体消除了MDA-MB-231细胞对HUVECs的增强粘附。重组人可溶性TF (rTF)结合β1整合素在HUVECs表面,β1或α3整合素抗体结合TF抗体可消除更多的细胞-细胞粘附。这些数据表明,TF介导的乳腺癌细胞与内皮细胞的粘附可能依赖于huvec表面的β1整合素。
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来源期刊
CiteScore
6.40
自引率
0.00%
发文量
7
审稿时长
53 weeks
期刊介绍: Cell Adhesion & Migration is a multi-disciplinary, peer reviewed open access journal that focuses on the biological or pathological implications of cell-cell and cell-microenvironment interactions. The main focus of this journal is fundamental science. The journal strives to serve a broad readership by regularly publishing review articles covering specific disciplines within the field, and by publishing focused issues that provide an overview on specific topics of interest within the field. Cell Adhesion & Migration publishes relevant and timely original research, as well as authoritative overviews, commentaries, and perspectives, providing context for the work presented in Cell Adhesion & Migration and for key results published elsewhere. Original research papers may cover all topics important in the field of cell-cell and cell-matrix interactions. Cell Adhesion & Migration also publishes articles related to cell biomechanics, biomaterial, and development of related imaging technologies.
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