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(I-3、II-3)-白杨素介导的细胞死亡涉及线粒体。

(I-3,II-3)-Biacacetin-mediated cell death involves mitochondria.

机构信息

Amrita School of Biotechnology, Amrita Vishwa Vidyapeetham, Amrita University, Amritapuri, Clappana P.O, Kollam, Kerala, 690525, India.

出版信息

Mol Cell Biochem. 2019 Jan;451(1-2):79-90. doi: 10.1007/s11010-018-3395-8. Epub 2018 Jul 2.

Abstract

Dysregulation of the dynamic balance between cell proliferation and cell death leads to several malignancies including cancer. Biflavones are known to possess anti-proliferative activity against numerous cancer cell lines. The current study was undertaken to understand the mechanism of action of the biflavonoid (I-3,II-3)-biacacetin on MDA-MB-231. Biacacetin induces dose-dependent cell death in MDA-MB-231 cells from concentrations as low as 0.5 μM, which was further confirmed by an increase in sub-G1 cells. Furthermore, the cell death induced by biacacetin was found to be mitochondria-dependent, since cells devoid of mitochondria were viable in the presence of biacacetin even at the highest concentration tested (25 μM). Fluorescence studies clearly indicated nuclear changes and apoptotic body formation that are characteristic of apoptosis. These results were further corroborated by studies that demonstrate biacacetin to regulate several key markers of apoptosis like Caspase 3, p53, Bax, and poly-ADP-ribose polymerase-1. Furthermore, biacacetin did not induce cell death in normal macrophage cell line, RAW at concentrations up to 15 μM. In addition to MDA-MB-231 cells, biacacetin also induces apoptotic cell death in the highly chemo-resistant cell line, OVISE, where the cells stained positive for annexin. Biacacetin also induces cell death in the highly malignant fibrosarcoma cell line HT1080. Furthermore, biacacetin also induces significant cell death (50%) in 3D tumor spheroids, at a concentration of 25 μM. Taken together, these results provide an understanding of biacacetin-mediated cell death and thereby provides a strong basis for the use of such compounds as novel templates for anti-cancer therapeutics.

摘要

细胞增殖和细胞死亡之间的动态平衡失调会导致多种恶性肿瘤,包括癌症。双黄酮类化合物已被证实对许多癌细胞系具有抗增殖活性。本研究旨在了解双黄酮(I-3,II-3)-双芹菜素对 MDA-MB-231 的作用机制。双芹菜素可诱导 MDA-MB-231 细胞从低至 0.5 μM 的浓度产生剂量依赖性细胞死亡,这可通过亚 G1 期细胞增加进一步证实。此外,发现双芹菜素诱导的细胞死亡是线粒体依赖性的,因为即使在测试的最高浓度(25 μM)下,缺乏线粒体的细胞在存在双芹菜素的情况下仍能存活。荧光研究清楚地表明了核变化和凋亡小体的形成,这是凋亡的特征。这些结果进一步得到了研究的证实,研究表明双芹菜素调节凋亡的几个关键标志物,如 Caspase 3、p53、Bax 和聚 ADP-核糖聚合酶-1。此外,双芹菜素在高达 15 μM 的浓度下不会诱导正常巨噬细胞 RAW 细胞系发生细胞死亡。除了 MDA-MB-231 细胞外,双芹菜素还可诱导高度耐药细胞系 OVISE 中的凋亡细胞死亡,细胞对 Annexin 染色呈阳性。双芹菜素还可诱导高度恶性纤维肉瘤细胞系 HT1080 中的细胞死亡。此外,双芹菜素在浓度为 25 μM 时还可诱导 3D 肿瘤球体中显著的细胞死亡(50%)。综上所述,这些结果提供了对双芹菜素介导的细胞死亡的理解,并为将此类化合物用作新型抗癌治疗的模板提供了坚实的基础。

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