Department of Veterinary Medicine, Research Institute of Life Science, Gyeongsang National University, Jinju 52828, Korea.
Biological Resources Research Group, Bioenvironmental Science & Toxicology Division, Korea Institute of Toxicology (KIT), 17 Jeigok-gil, Jinju 52834, Korea.
Cells. 2022 Sep 1;11(17):2734. doi: 10.3390/cells11172734.
Apigetrin (7-(β-D-glucopyranosyloxy)-4',5-dihydroxyflavone), a glycoside bioactive dietary flavonoid derived from and is known to possess anticancer, antioxidant, and anti-inflammatory effects on numerous cancers. In the present study, we examined the effect of apigetrin in Hep3B hepatocellular cancer cell line (HCC). Apigetrin inhibited cell growth and proliferation of Hep3B cells, as confirmed by MTT and colony formation assay. We used apigetrin at concentrations of 0, 50, and 100 µM for later experiments. Of these concentrations, 100 µM of apigetrin showed a significant effect on cell inhibition. In apigetrin-treated Hep3B cells, cell cycle arrest occurred at the G2/M phase. Apoptosis and necroptosis of Hep3B cells treated with apigetrin were confirmed by Annexin V/propidium iodide (PI) staining and flow cytometry results. Morphological observation through 4',6-diamidino-2-phenylindole (DAPI) staining showed intense blue fluorescence representing chromatin condensation. Hematoxylin staining showed necroptotic features such as formation of vacuoles and swelling of organelles. Apigetrin increased reactive oxygen species (ROS) levels in cells, based on fluorescence imaging. Furthermore, the underlying mechanism involved in the apoptosis and necroptosis was elucidated through western blotting. Apigetrin up-regulated TNFα, but down-regulated phosphorylation of p-p65, and IκB. Apigetrin inhibited the expression of Bcl-xl but increased Bax levels. Up-regulation of cleaved PARP and cleaved caspase 3 confirmed the induction of apoptosis in apigetrin-treated Hep3B cells. Additionally, necroptosis markers RIP3, p-RIP3, and p-MLKL were significantly elevated by apigetrin dose-dependently, suggesting necroptotic cell death. Taken together, our findings strongly imply that apigetrin can induce apoptosis and necroptosis of Hep3B hepatocellular cancer cells. Thus, apigetrin as a natural compound might have potential for treating liver cancer.
芹菜素(7-(β-D-吡喃葡萄糖基氧基)-4',5-二羟基黄酮),一种糖苷类生物活性膳食类黄酮,来源于 和 ,已知具有抗癌、抗氧化和抗炎症作用,对许多癌症都有作用。在本研究中,我们研究了芹菜素对 Hep3B 肝癌细胞系(HCC)的影响。MTT 和集落形成实验证实,芹菜素抑制 Hep3B 细胞的生长和增殖。我们使用浓度为 0、50 和 100µM 的芹菜素进行后续实验。在这些浓度中,100µM 的芹菜素对细胞抑制作用有显著影响。在芹菜素处理的 Hep3B 细胞中,细胞周期停滞在 G2/M 期。通过 Annexin V/碘化丙啶(PI)染色和流式细胞术结果证实,芹菜素处理的 Hep3B 细胞发生凋亡和坏死性凋亡。通过 4',6-二脒基-2-苯基吲哚(DAPI)染色进行形态学观察,显示出强烈的蓝色荧光,代表染色质浓缩。苏木精染色显示出坏死性凋亡的特征,如空泡形成和细胞器肿胀。通过荧光成像显示,芹菜素增加了细胞内的活性氧(ROS)水平。此外,通过蛋白质印迹法阐明了凋亡和坏死性凋亡的潜在机制。芹菜素上调 TNFα,但下调磷酸化 p-p65 和 IκB。芹菜素抑制 Bcl-xl 的表达,但增加 Bax 水平。活化的 PARP 和 cleaved caspase 3 的上调证实了凋亡诱导在芹菜素处理的 Hep3B 细胞中。此外,坏死性凋亡标志物 RIP3、p-RIP3 和 p-MLKL 被芹菜素剂量依赖性地显著上调,表明发生了坏死性细胞死亡。综上所述,我们的研究结果强烈暗示芹菜素可以诱导 Hep3B 肝癌细胞的凋亡和坏死性凋亡。因此,芹菜素作为一种天然化合物可能具有治疗肝癌的潜力。