Wang Chunfeng, Wang Na, Li Na, Yu Qiuying, Wang Fangyu
The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Zhengzhou Nutrition and Health Food Laboratory, Zhengzhou, China.
Front Pharmacol. 2021 Nov 3;12:760919. doi: 10.3389/fphar.2021.760919. eCollection 2021.
Resveratrol (RES) and Vitamin E (VE) are anti-cancer active ingredients with relatively high content in peanut seeds and sprouts. This study aimed to determine the synergistic inhibitory effect of RES and VE on colorectal cancer. Using 5-FU as a positive drug control, the effect of RES combined with VE on HCT-8 cells was determined, and cell viability was detected using the cell-counting kit 8 (CCK8) method. Cell morphology changes were observed using optical microscopy. Cell migration ability was evaluated by the scratch test, while cell colonies were determined by the cloning test formation ability. Apoptosis status was assessed by flow cytometry and nuclear staining by DAPI, and the expression level of apoptosis-related proteins was determined by western blotting. Compared with the single component group, the RES combined with VE group significantly inhibited the growth and proliferation of HCT-8 intestinal cancer cells . The RES combined with VE group had a greater impact on cell morphology changes and cell colony formation and significantly reduced cell migration ability and intestinal cancer cell apoptosis ( < 0.05). Additionally, combined treatment with RES and VE significantly upregulated the expression of pro-apoptotic proteins BAX, caspase-3, caspase-8, and caspase-9, and downregulated the expression of anti-apoptotic protein BCL-2, compared to the single component treatment. RES combined with VE is effective in promoting intestinal cancer cell apoptosis. This study demonstrated the significant positive synergy of RES and VE on HCT-8 cells, providing a new perspective for more effective use of RES.
白藜芦醇(RES)和维生素E(VE)是花生种子和芽中含量相对较高的抗癌活性成分。本研究旨在确定RES和VE对结直肠癌的协同抑制作用。以5-氟尿嘧啶作为阳性药物对照,测定RES与VE联合对HCT-8细胞的作用,并采用细胞计数试剂盒8(CCK8)法检测细胞活力。使用光学显微镜观察细胞形态变化。通过划痕试验评估细胞迁移能力,通过克隆试验形成能力测定细胞集落。通过流式细胞术和DAPI核染色评估细胞凋亡状态,并通过蛋白质印迹法测定凋亡相关蛋白的表达水平。与单一组分组相比,RES联合VE组显著抑制HCT-8肠癌细胞的生长和增殖。RES联合VE组对细胞形态变化和细胞集落形成有更大影响,并显著降低细胞迁移能力和肠癌细胞凋亡(P<0.05)。此外,与单一组分处理相比,RES和VE联合处理显著上调促凋亡蛋白BAX、caspase-3、caspase-8和caspase-9的表达,并下调抗凋亡蛋白BCL-2的表达。RES联合VE可有效促进肠癌细胞凋亡。本研究证明了RES和VE对HCT-8细胞具有显著的正向协同作用,为更有效地利用RES提供了新的视角。