Sudha A, Srinivasan P, Kanimozhi V, Palanivel K, Kadalmani B
a Department of Bioinformatics , Alagappa University , Karaikudi , India.
b Department of Animal Health and Management , Alagappa University , Karaikudi , India.
J Recept Signal Transduct Res. 2018 Jun;38(3):179-190. doi: 10.1080/10799893.2018.1468780. Epub 2018 May 8.
The aim of this study was to find the efficacy of 5-hydroxy 3',4',7-trimethoxyflavone (HTMF), a flavonoid compound isolated from the medicinal plant Lippia nodiflora, in inhibiting the proliferation and inducing apoptosis in human breast cancer cell line MCF-7. The anti-proliferative effect of the compound HTMF was confirmed using MTT cytotoxicity assay. Increased apoptotic induction by HTMF was demonstrated by acridine orange/ethidium bromide (AO/EtBr) and Hoechst 33258 staining studies. The phosphatidylserine translocation, an early feature of apoptosis and DNA damage were revealed through AnnexinV-Cy3 staining and comet assay. Moreover, the significant elevation of cellular ROS was observed in the treated cells, as measured by 2,7-diacetyl dichlorofluorescein (DCFH-DA). The mRNA expression studies also supported the effectiveness of HTMF by shifting the Bax:Bcl-2 ratio. The treatment of MCF-7 cells with HTMF encouraged apoptosis through the modulation of apoptotic markers, such as p53, Bcl-2, Bax, and cleaved PARP. In silico molecular docking and dynamics studies with MDM2-p53 protein revealed that HTMF was more potent compound that could inhibit the binding of MDM2 with p53 and, therefore, could trigger apoptosis in cancer cell. Overall, this study brings up scientific evidence for the efficacy of HTMF against MCF-7 breast cancer cells.
本研究的目的是探究从药用植物节节草中分离出的黄酮类化合物5-羟基3',4',7-三甲氧基黄酮(HTMF)对人乳腺癌细胞系MCF-7增殖的抑制作用及诱导凋亡的效果。采用MTT细胞毒性试验证实了化合物HTMF的抗增殖作用。通过吖啶橙/溴化乙锭(AO/EtBr)和Hoechst 33258染色研究证明HTMF增强了凋亡诱导作用。通过膜联蛋白V-Cy3染色和彗星试验揭示了凋亡早期特征磷脂酰丝氨酸易位和DNA损伤。此外,用2,7-二乙酰二氯荧光素(DCFH-DA)测定发现,处理后的细胞中细胞活性氧显著升高。mRNA表达研究也通过改变Bax:Bcl-2比值支持了HTMF的有效性。用HTMF处理MCF-7细胞通过调节凋亡标志物(如p53、Bcl-2、Bax和裂解的PARP)促进凋亡。与MDM2-p53蛋白进行的计算机分子对接和动力学研究表明,HTMF是一种更有效的化合物,能够抑制MDM2与p53的结合,因此能够触发癌细胞凋亡。总体而言,本研究为HTMF对MCF-7乳腺癌细胞的疗效提供了科学证据。