Ling Lu, Mulligan Jeffrey A, Ouyang Yunxin, Shimpi Adrian A, Williams Rebecca M, Beeghly Garrett F, Hopkins Benjamin D, Spector Jason A, Adie Steven G, Fischbach Claudia
Nancy E. and Peter C. Meinig School of Biomedical Engineering, Cornell University, Ithaca, New York, 14853, USA.
School of Electrical and Computer Engineering, Cornell University, Ithaca, New York, 14853, USA.
Adv Funct Mater. 2020 Nov 25;30(48). doi: 10.1002/adfm.201910650. Epub 2020 May 4.
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 were 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 (OCT) 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.
肥胖会增加患乳腺癌的风险并使预后恶化,部分原因是脂肪基质细胞(ASC)行为的改变。然而,肥胖个体的ASC相对于瘦个体的ASC是否会增加乳腺癌细胞的迁移,目前尚不清楚。为了验证这种联系,将由具有不同恶性潜能的MCF10A衍生肿瘤细胞系以及瘦或肥胖ASC组成的多细胞球体嵌入模拟乳腺间质脂肪组织弹性模量的胶原支架中。共聚焦图像分析表明,在这些条件下,单独的肿瘤细胞迁移不明显。然而,与瘦或肥胖ASC的直接细胞间接触使它们能够集体迁移,其中肥胖ASC比瘦ASC更有效地激活肿瘤细胞迁移。时间分辨光学相干断层扫描(OCT)成像表明,肥胖ASC通过介导局部胶原纤维的收缩促进肿瘤细胞迁移。基质金属蛋白酶(MMP)依赖性蛋白水解活性显著促进ASC介导的肿瘤细胞侵袭和胶原变形。然而,ASC的收缩性也很重要,因为同时抑制MMP和收缩性对于完全消除ASC介导的肿瘤细胞迁移是必要的。这些发现表明,肥胖介导的ASC表型变化可能影响肿瘤细胞的迁移和侵袭,对肥胖患者的乳腺癌恶性程度具有潜在影响。