Source abstract
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.
Source: crossref · Quality: baseline
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