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评论,“2-甲氧基雌二醇通过下调 HIF-1α 增敏他莫昔芬耐药 MCF-7 乳腺癌细胞”。

Comment on, "2-methoxyestradiol sensitizes tamoxifen-resistant MCF-7 breast cancer cells via downregulating HIF-1α".

机构信息

Lab in Biotechnology and Biosignal Transduction, Department of Orthodontics, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, 77, Tamil Nadu, India.

Lab in Biotechnology and Biosignal Transduction, Department of Orthodontics, Saveetha Dental College and Hospital, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, 77, Tamil Nadu, India.

出版信息

Surgeon. 2024 Dec;22(6):e240-e241. doi: 10.1016/j.surge.2024.09.004. Epub 2024 Sep 21.

Abstract

This study investigates the potential of 2-methoxyestradiol (2-ME) to overcome tamoxifen (TAM) resistance in MCF-7 breast cancer cells by downregulating hypoxia-inducible factor 1 alpha (HIF-1α). Through a series of in vitro experiments, the authors demonstrate that combining 2-ME with TAM enhances the cytotoxic effects on resistant cells, increases apoptosis markers, and reduces cholesterol and triglyceride levels. While the findings highlight a promising therapeutic approach, the lack of in vivo or clinical data limits direct clinical application. Future research should focus on validating these results in animal models and exploring long-term efficacy and molecular mechanisms.

摘要

本研究通过下调缺氧诱导因子 1 ɑ(HIF-1α),探讨了 2-甲氧基雌二醇(2-ME)克服 MCF-7 乳腺癌细胞中他莫昔芬(TAM)耐药的潜力。通过一系列体外实验,作者证明 2-ME 与 TAM 联合使用可增强对耐药细胞的细胞毒性作用,增加凋亡标志物,并降低胆固醇和甘油三酯水平。尽管这些发现强调了一种有前途的治疗方法,但缺乏体内或临床数据限制了其直接临床应用。未来的研究应集中在动物模型中验证这些结果,并探索长期疗效和分子机制。

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