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间充质干细胞通过转化生长因子-β诱导侵袭性乳腺癌细胞的定向迁移。

Mesenchymal Stem Cells Induce Directional Migration of Invasive Breast Cancer Cells through TGF-β.

作者信息

McAndrews Kathleen M, McGrail Daniel J, Ravikumar Nithin, Dawson Michelle R

机构信息

School of Chemical &Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.

The Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332, USA.

出版信息

Sci Rep. 2015 Nov 20;5:16941. doi: 10.1038/srep16941.

Abstract

Mesenchymal stem cells (MSCs) are recruited to the tumor microenvironment and influence tumor progression; however, how MSCs induce the invasion of cancer cells is not completely understood. Here, we used a 3D coculture model to determine how MSCs affect the migration of invasive breast cancer cells. Coculture with MSCs increases the elongation, directional migration, and traction generation of breast cancer cells. MSC-induced directional migration directly correlates with traction generation and is mediated by transforming growth factor β (TGF-β) and the migratory proteins rho-associated kinase, focal adhesion kinase, and matrix metalloproteinases. Treatment with MSC conditioned media or recombinant TGF-β1 elicits a similar migration response to coculture. Taken together, this work suggests TGF-β is secreted by MSCs, leading to force-dependent directional migration of invasive breast cancer cells. These pathways may be potential targets for blocking cancer cell invasion and subsequent metastasis.

摘要

间充质干细胞(MSCs)被募集到肿瘤微环境中并影响肿瘤进展;然而,MSCs如何诱导癌细胞侵袭尚未完全明确。在此,我们使用三维共培养模型来确定MSCs如何影响侵袭性乳腺癌细胞的迁移。与MSCs共培养可增加乳腺癌细胞的伸长、定向迁移和牵引力产生。MSCs诱导的定向迁移与牵引力产生直接相关,并由转化生长因子β(TGF-β)以及迁移蛋白 Rho相关激酶、粘着斑激酶和基质金属蛋白酶介导。用MSCs条件培养基或重组TGF-β1处理可引发与共培养类似的迁移反应。综上所述,这项研究表明TGF-β由MSCs分泌,导致侵袭性乳腺癌细胞发生力依赖性定向迁移。这些通路可能是阻断癌细胞侵袭及后续转移的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df7/4653660/505963a30852/srep16941-f1.jpg

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