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雌激素相关受体α(ERRα)促进乳腺癌中癌症干细胞样特征。

Estrogen-Related Receptor Alpha (ERRα) Promotes Cancer Stem Cell-Like Characteristics in Breast Cancer.

机构信息

School of Biotechnology, Kalinga Institute of Industrial Technology (KIIT), Deemed to be University, Bhubaneswar, Odisha, 751024, India.

出版信息

Stem Cell Rev Rep. 2023 Nov;19(8):2807-2819. doi: 10.1007/s12015-023-10605-2. Epub 2023 Aug 16.

Abstract

Cancer stem cells drive tumor initiation, invasion, metastasis and recurrence. In the present study, we have evaluated the role of ERRα in the maintenance of breast cancer stem cells (BCSCs) using breast cancer cell lines. The inhibition of ERRα with the inverse agonist, XCT-790, or the knockdown of ERRα in breast cancer cells significantly reduced the mammosphere formation efficiency and mammosphere size along with a significant reduction in the CD44/CD24 BCSCs. Treatment with XCT-790 significantly downregulated expression of the transcription factors involved in stem cell maintenance such as Oct4, Klf4, Sox2, Nanog and c-Myc in the mammosphere forming stem cells of MCF7 and MDA-MB-231. In addition, XCT-790 induced cell cycle arrest and apoptosis in the mammosphere-forming cells. The knockdown or inhibition of ERRα downregulated the expression of Notch1 and β-catenin, whereas the overexpression of ERRα in MCF7 cells upregulated the expression of these proteins. Moreover, the inhibition of ERRα synergistically enhanced the efficacy of paclitaxel in inhibiting the BCSCs. These results show that ERRα is crucial for the maintenance of BCSCs and suggest that ERRα could be a potential target for breast cancer treatment.

摘要

癌症干细胞驱动肿瘤的发生、侵袭、转移和复发。在本研究中,我们使用乳腺癌细胞系评估了 ERRα 在维持乳腺癌干细胞(BCSCs)中的作用。用反向激动剂 XCT-790 抑制 ERRα,或在乳腺癌细胞中敲低 ERRα,均可显著降低乳腺球形成效率和乳腺球大小,同时 CD44/CD24 BCSCs 显著减少。用 XCT-790 处理可显著下调 MCF7 和 MDA-MB-231 的乳腺球形成干细胞中参与干细胞维持的转录因子的表达,如 Oct4、Klf4、Sox2、Nanog 和 c-Myc。此外,XCT-790 诱导乳腺球形成细胞的细胞周期停滞和凋亡。敲低或抑制 ERRα 下调 Notch1 和 β-catenin 的表达,而 MCF7 细胞中 ERRα 的过表达则上调这些蛋白的表达。此外,抑制 ERRα 可协同增强紫杉醇抑制 BCSCs 的效果。这些结果表明 ERRα 对于维持 BCSCs 至关重要,并表明 ERRα 可能是乳腺癌治疗的潜在靶点。

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