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螺旋山芹内酯 II 通过内质网途径诱导乳腺癌细胞周期停滞和凋亡。

Atractylenolide II induces cell cycle arrest and apoptosis in breast cancer cells through ER pathway.

机构信息

Colleges of Life Science and Technology, Dalian University, Dalian Economic-Technological Development Zone, Liaoning, China.

Huiqiao Medical Center, Nanfang Hospital, Southern Medical University, Guangzhou, China.

出版信息

Pak J Pharm Sci. 2021 Jul;34(4):1449-1458.

Abstract

In this research, atractylenolide II (ATR II) on apoptosis, cell cycle cells via ER pathway in breast cancer (MDA-MB-231 and MCF-7) cells are assessed. The effect of ATR II on cell proliferation was detected by MTT assay. Additional flow cytometry, luciferase, the western blot were performed to detect the signaling pathway cytotoxicity of ATR II. We have also carried out autodock measurements to validate our results. Our findings showed ATR II could inhibit breast cancer cell growth by apoptosis mainly through G2/M-phase cell cycle arrest. Besides, the cytotoxicity of ATTR II on breast cancer was also correlated by the regulation of endrogen receptors and promising an anti-inflammatory activity via inhibiting NF-KB signaling pathways. Taking together, ATR II could be a potential anti-cancer drug for breast cancer.

摘要

本研究通过内质网(ER)通路评估了白术内酯 II(ATR II)对乳腺癌(MDA-MB-231 和 MCF-7)细胞凋亡和细胞周期的影响。通过 MTT 检测法检测 ATR II 对细胞增殖的影响。另外,还进行了流式细胞术、荧光素酶和 Western blot 实验来检测 ATR II 的细胞毒性信号通路。我们还进行了自动对接测量以验证我们的结果。我们的研究结果表明,ATR II 主要通过 G2/M 期细胞周期阻滞抑制乳腺癌细胞生长,诱导细胞凋亡。此外,ATR II 对乳腺癌的细胞毒性也与雌激素受体的调节有关,并通过抑制 NF-KB 信号通路显示出有希望的抗炎活性。综上所述,ATR II 可能成为治疗乳腺癌的一种潜在的抗癌药物。

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