journal article·2020-11Open access

Obesity‐Associated Adipose Stromal Cells Promote Breast Cancer Invasion through Direct Cell Contact and ECM Remodeling

Lu Ling, Jeffrey A. Mulligan, Yunxin Ouyang, Adrian A. Shimpi, Rebecca M. Williams, Garrett F. Beeghly, Benjamin D. Hopkins, Jason A. Spector, Steven G. Adie, Claudia Fischbach

Advanced Functional Materials· Volume 30· Issue 48

Abstract

Abstract Obesity increases the risk and worsens the prognosis for breast cancer due, in part, to altered adipose stromal cell (ASC) behavior. Whether ASCs from obese individuals increase migration of breast cancer cells relative to their lean counterparts, however, remains unclear. To test this connection, multicellular spheroids composed of MCF10A‐derived tumor cell lines of varying malignant potential and lean or obese ASCs are embedded into collagen scaffolds mimicking the elastic moduli of interstitial breast adipose tissue. Confocal image analysis suggests that tumor cells alone migrate insignificantly under these conditions. However, direct cell‐cell contact with either lean or obese ASCs enables them to migrate collectively, whereby obese ASCs activate tumor cell migration more effectively than their lean counterparts. Time‐resolved optical coherence tomography imaging suggests that obese ASCs facilitate tumor cell migration by mediating contraction of local collagen fibers. Matrix metalloproteinase (MMP)‐dependent proteolytic activity significantly contributes to ASC‐mediated tumor cell invasion and collagen deformation. However, ASC contractility is also important, as co‐inhibition of both MMPs and contractility is necessary to completely abrogate ASC‐mediated tumor cell migration. These findings imply that obesity‐mediated changes of ASC phenotype may impact tumor cell migration and invasion with potential implications for breast cancer malignancy in obese patients.
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Research context

OpenAlex topics: Cancer Cells and Metastasis · Cellular Mechanics and Interactions · Lymphatic System and Diseases

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Nancy E. and Peter C. Meinig School of Biomedical Engineering Cornell University Ithaca NY 14853 USA

School of Electrical and Computer Engineering Cornell University Ithaca NY 14853 USA

Institute of Biotechnology Cornell University Ithaca NY 14853 USA

Meyer Cancer Center Weill Cornell Medicine New York NY 10021 USA

Department of Oncological Sciences Icahn School of Medicine at Mount Sinai New York NY 10029 USA

Division of Plastic Surgery Weill Cornell Medicine New York NY 10021 USA

Kavli Institute at Cornell for Nanoscale Science Cornell University Ithaca NY 14853 USA

Funding

Materials Research Science and Engineering Center, Harvard University · National Science Foundation · New York State Stem Cell Science · National Institutes of Health

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