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脂肪细胞在乳腺肿瘤细胞中诱导独特的基因表达谱,并增强浸润性乳腺癌细胞中的炎症信号。

Adipocytes induce distinct gene expression profiles in mammary tumor cells and enhance inflammatory signaling in invasive breast cancer cells.

机构信息

Institute of Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University Hospital Leipzig, Leipzig, Germany.

LIFE Leipzig Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.

出版信息

Sci Rep. 2018 Jun 21;8(1):9482. doi: 10.1038/s41598-018-27210-w.

Abstract

Obesity is a known risk factor for breast cancer. Since obesity rates are constantly rising worldwide, understanding the molecular details of the interaction between adipose tissue and breast tumors becomes an urgent task. To investigate potential molecular changes in breast cancer cells induced by co-existing adipocytes, we used a co-culture system of different breast cancer cell lines (MCF-7 and T47D: ER/PR/HER2 and MDA-MB-231: ER/PR/HER2) and murine 3T3-L1 adipocytes. Here, we report that co-culture with adipocytes revealed distinct changes in global gene expression pattern in the different breast cancer cell lines. Our microarray data revealed that in both ER cell lines, top upregulated genes showed significant enrichment for hormone receptor target genes. In triple-negative MDA-MB-231 cells, co-culture with adipocytes led to the induction of pro-inflammatory genes, mainly involving genes of the Nf-κB signaling pathway. Moreover, co-cultured MDA-MB-231 cells showed increased secretion of the pro-inflammatory interleukins IL-6 and IL-8. Using a specific NF-κB inhibitor, these effects were significantly decreased. Finally, migratory capacities were significantly increased in triple-negative breast cancer cells upon co-culture with adipocytes, indicating an enhanced aggressive cell phenotype. Together, our studies illustrate that factors secreted by adipocytes have a significant impact on the molecular biology of breast cancer cells.

摘要

肥胖是乳腺癌的已知风险因素。由于全球肥胖率不断上升,了解脂肪组织和乳腺癌肿瘤之间相互作用的分子细节成为当务之急。为了研究共存脂肪细胞诱导的乳腺癌细胞中潜在的分子变化,我们使用了不同乳腺癌细胞系(MCF-7 和 T47D:ER/PR/HER2 和 MDA-MB-231:ER/PR/HER2)和小鼠 3T3-L1 脂肪细胞的共培养系统。在这里,我们报告说,与脂肪细胞共培养揭示了不同乳腺癌细胞系中全局基因表达模式的明显变化。我们的微阵列数据显示,在两种 ER 细胞系中,上调基因的主要富集涉及激素受体靶基因。在三阴性 MDA-MB-231 细胞中,与脂肪细胞共培养导致促炎基因的诱导,主要涉及 NF-κB 信号通路的基因。此外,共培养的 MDA-MB-231 细胞显示促炎细胞因子 IL-6 和 IL-8 的分泌增加。使用特定的 NF-κB 抑制剂,这些作用显著降低。最后,三阴性乳腺癌细胞在与脂肪细胞共培养时迁移能力显著增加,表明侵袭性细胞表型增强。总之,我们的研究表明脂肪细胞分泌的因子对乳腺癌细胞的分子生物学有重大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96f9/6013441/e2c1f323226e/41598_2018_27210_Fig1_HTML.jpg

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