乳腺癌细胞系MCF-7与脂肪组织间充质干细胞共培养中参与上皮-间充质转化的转录因子的表达

Vu Thi Tien, Le Hoang Duc, Bui Van Ngoc, Nguyen Trung Nam
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引用次数: 0

摘要

乳腺癌是全球女性中最常见的癌症。肿瘤微环境在上皮-间质转化(epithelial-to-mesenchymal transition, EMT)过程中起着至关重要的作用,导致癌细胞的侵袭和转移。肿瘤微环境包括肿瘤细胞的所有组成部分,包括细胞外基质、肿瘤血管、间充质干细胞、免疫细胞和成纤维细胞。了解间充质干细胞和癌细胞之间的相互作用对于确定间充质干细胞在乳腺癌诊断和治疗中的作用至关重要。在这项研究中,我们展示了脂肪组织间充质干细胞(ADMSCs)和乳腺癌细胞(MCF-7细胞系)共培养的结果,并确定了参与EMT的转录因子的表达水平,包括Twist和Snail。结果表明,与单独培养的MCF-7相比,MCF-7与ADMSCs共培养的增殖没有增加。通过qRT-PCR检测基因表达水平发现,与ADMSCs共培养后,乳腺癌细胞中emt相关转录因子(Twist和Snail)显著增加。与ADMSCs共培养的MCF-7细胞与单独培养的MCF-7细胞中IL-6和AhR的表达水平也有显著差异。结果表明,ADMSCs可能通过AhR/NF-κB通路促进MCF-7细胞的EMT。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression of transcription factors involved in epithelial-to-mesenchymal transition of the breast cancer cell line MCF-7 co-cultured with adipose tissue mesenchymal stem cells
Breast cancer is the most frequently diagnosed cancer in women globally. The tumor microenvironment plays a vital role in epithelial-to-mesenchymal transition (EMT), leading to the invasion and metastasis of cancer cells. The tumor microenvironment includes all components of the tumor cells, including the extracellular matrix, tumor vasculature, mesenchymal stem cells, immune cells, and fibroblasts. Understanding the interactions between mesenchymal stem cells and cancer cells is essential in determining the role of mesenchymal stem cells in diagnosing and treating breast cancer. In this study, we present the result of co-culture between adipose tissue mesenchymal stem cells (ADMSCs) and breast cancer cells (MCF-7 cell line) and determine the expression levels of transcription factors involved in EMT, including Twist and Snail. The results showed that the proliferation of MCF-7 co-cultured with ADMSCs was not increased compared to MCF-7 mono-cultured. Determination of gene expression levels by qRT-PCR revealed a significant increase in the EMT-related transcription factors (Twist and Snail) in breast cancer cells upon co-culture with ADMSCs. There were also significant differences between the expression levels of IL-6 and AhR in MCF-7 cells co-cultured with ADMSCs and MCF-7 cells mono-cultured. The results suggested that ADMSCs promoted the EMT of MCF-7 cells, potentially via AhR/NF-κB pathways.
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