McAndrews Kathleen M, McGrail Daniel J, Ravikumar Nithin, Dawson Michelle R
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.
Sci Rep. 2015 Nov 20;5:16941. doi: 10.1038/srep16941.
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.
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。