Celine Chelsea Hartono, Janti Sudiono, Pretty Trisfilha
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引用次数: 0
摘要
背景:Borassus flabellifer L.果实的种皮中含有抗氧化剂,可以中和自由基的毒性作用,并能对抗因暴露于氧化应激而造成的 DNA 损伤。经证实,花叶鲍鱼提取物具有细胞毒性作用,可抑制几种癌细胞(如 HeLa 细胞系)的生长。研究目的测定 B. flabellifer L. 果实种皮提取物对 HSC-3 细胞系的细胞毒性作用。方法:以 HSC-3 细胞系为研究对象,进行实验室实验研究:使用浓度为 93.75 µg/mL、187.5 µg/mL、375 µg/mL、750 µg/mL 和 1,500 µg/mL 的 B. flabellifer L. 果实种皮提取物处理 HSC-3 细胞系,阴性对照 DMEM-FBS 20%,阳性对照抗癌药物多柔比星 3 µM。使用 CCK-8 试剂对 HSC-3 细胞株进行细胞毒性检测。使用波长为 450 nm 的微孔平板阅读器通过测量甲状腺素的光密度来确定 HSC-3 细胞株的存活率。结果在浓度为 93.75 微克/毫升、187.5 微克/毫升、375 微克/毫升、750 微克/毫升和 1,500 微克/毫升时,B. flabellifer 果实 L. 种皮提取物能够降低 HSC-3 细胞株的活力并具有细胞毒性,IC50 值为 141.9 微克/毫升。结论B. flabellifer L.果实种皮提取物的细胞毒性作用可抑制细胞增殖,从而降低 HSC-3 细胞系癌细胞的存活能力。
Effects of Borassus flabellifer L. fruit seed coat on HSC-3 cell line
Background: The seed coat of Borassus flabellifer L. fruit contains antioxidants that can neutralize the toxic effects of free radicals and can fight DNA damage due to exposure to oxidative stress. The extract of B. flabellifer is proven to have cytotoxic effects and can inhibit the growth of several types of cancer cells such as HeLa cell lines. Objective: To determine the cytotoxicity effect of extract of B. flabellifer L. fruit seed coat against HSC-3 cell line. Methods: Laboratory experimental research was conducted using HSC-3 cell lines treated with B. flabellifer L. fruit seed coat extract at concentrations of 93.75 µg/mL, 187.5 µg/mL, 375 µg/mL, 750 µg/mL, and 1,500 µg/mL, negative control DMEM-FBS 20%, and positive control anti cancer drugs Doxorubicin 3 µM. HSC-3 cell line cytotoxicity assay was performed using CCK-8 reagent. Micro plate reader at 450 nm wavelength was used to determine the viability of HSC-3 cell lines by measuring the optical density of formazan. Results: B. flabellifer fruit L. seed coat extract was able to reduce viability and was cytotoxic to HSC-3 cell lines at concentrations of 93.75 µg/mL, 187.5 µg/mL, 375 µg/mL, 750 µg/mL, and 1,500 µg/mL, with an IC50 value of 141.9 µg/mL. Conclusion: B. flabellifer L. fruit seed coat extract can reduce the ability of HSC-3 cell line cancer cells to survive by inhibiting cell proliferation due to its cytotoxicity effect.