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首页> 外文期刊>Oncogene >Interleukin 6 secreted from adipose stromal cells promotes migration and invasion of breast cancer cells
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Interleukin 6 secreted from adipose stromal cells promotes migration and invasion of breast cancer cells

机译:脂肪基质细胞分泌的白介素6促进乳腺癌细胞的迁移和侵袭

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摘要

Excessive adiposity has long been associated with increased incidence of breast cancer in post-menopausal women, and with increased mortality from breast cancer, regardless of the menopausal status. Although adipose tissue-derived estrogen contributes to obesity-associated risk for estrogen receptor (ER)-positive breast cancer, the estrogen-independent impact of adipose tissue on tumor invasion and progression needs to be elucidated. Here, we show that adipose stromal cells (ASCs) significantly stimulate migration and invasion of ER-negative breast cancer cells in vitro and tumor invasion in a co-transplant xenograft mouse model. Our study also identifies cofilin-1, a known regulator of actin dynamics, as a determinant of the tumor-promoting activity of ASCs. The cofilin-1-dependent pathway affects the production of interleukin 6 (IL-6) in ASCs. Depletion of IL-6 from the ASC-conditioned medium abrogated the stimulatory effect of ASCs on the migration and invasion of breast tumor cells. Thus, our study uncovers a link between a cytoskeleton-based pathway in ASCs and the stromal impact on breast cancer cells.
机译:长期以来,肥胖症与绝经后妇女乳腺癌的发病率增加以及与乳腺癌的死亡率增加有关,而与绝经状态无关。尽管源自脂肪组织的雌激素会导致肥胖相关的雌激素受体(ER)阳性乳腺癌风险,但仍需要阐明脂肪组织对肿瘤侵袭和进展的非雌激素依赖性影响。在这里,我们显示出脂肪基质细胞(ASCs)在体外共同移植异种移植小鼠模型中显着刺激ER阴性乳腺癌细胞的迁移和侵袭以及肿瘤侵袭。我们的研究还鉴定了肌动蛋白动力学的已知调节剂cofilin-1,作为ASCs促肿瘤活性的决定因素。依赖cofilin-1的途径影响ASC中白介素6(IL-6)的产生。 ASC条件培养基中IL-6的消耗消除了ASC对乳腺肿瘤细胞迁移和侵袭的刺激作用。因此,我们的研究揭示了ASC中基于细胞骨架的途径与对乳腺癌细胞的基质作用之间的联系。

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