Citrus sinensis Peel Extract Synergistically Enhances the Cytotoxic Effect of Chemotherapeutic Agents on HepG2 Cells

Shofa Khamdanatuz Zufairo, D. Rahmawati, E. Meiyanto, R. A. Susidarti
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Abstract

Doxorubicin (DOX) and cisplatin (Cis), non-specific chemotherapeutic agents used for hepatocellular carcinoma (HCC), are frequently combined with synthetic or natural agents to enhance their cytotoxic effects. Citrus sinensis peel extract (CPE) serves as a natural source of flavonoids, including sinensetin (SIN), which has the potential to increase the efficacy of DOX and Cis. This study aimed to observe the effect of CPE and SIN one of CPE compounds, in enhancing liver cancer cell susceptibility to doxorubicin and cisplatin. The assays conducted in this study included a phytochemical analysis of CPE using TLC, cell viability assays against HepG2 cells using MTT assay in both single and combination forms, and cell viability assays on Vero cells. The result confirmed the presence of SIN as one of the compounds in CPE. Both CPE and SIN, when used individually, exhibited moderate cytotoxic effects on HepG2 cells with IC50 of 101.09 μg/mL and 83.13 μM, respectively, while showing no cytotoxic effect on Vero cells. Cis demonstrated significant cytotoxicity against HepG2 cells with an IC50 of 7.86 μM. DOX exerted a strong cytotoxic effect on both HepG2 and Vero cells, with the IC50 of 2.52 μM and 13.98 μM. It was observed that CPE was able to synergistically enhance the cytotoxic effects of DOX, and SIN synergistically increased the cytotoxicity of Cis, particularly against HepG2 cells, with CI<1.0.Keywords: CPE, SIN, Cisplatin, Doxorubicin, HCC.
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柑橘果皮提取物可协同增强化疗药物对 HepG2 细胞的细胞毒性作用
多柔比星(DOX)和顺铂(Cis)是治疗肝细胞癌(HCC)的非特异性化疗药物,经常与合成或天然药物结合使用,以增强其细胞毒性作用。柑橘皮提取物(CPE)是黄酮类化合物的天然来源,包括山奈苷(SIN),它有可能提高 DOX 和 Cis 的疗效。本研究旨在观察 CPE 和 CPE 复合物之一 SIN 在增强肝癌细胞对多柔比星和顺铂的敏感性方面的作用。本研究中进行的检测包括使用 TLC 对 CPE 进行植物化学分析,使用 MTT 法检测单个和组合形式的 HepG2 细胞的细胞活力,以及 Vero 细胞的细胞活力检测。结果证实,SIN 是 CPE 中的一种化合物。CPE 和 SIN 单独使用时,对 HepG2 细胞有中等程度的细胞毒性作用,IC50 分别为 101.09 μg/mL 和 83.13 μM,但对 Vero 细胞无细胞毒性作用。Cis 对 HepG2 细胞具有明显的细胞毒性,IC50 为 7.86 μM。DOX 对 HepG2 和 Vero 细胞都有很强的细胞毒性作用,IC50 分别为 2.52 μM 和 13.98 μM。研究发现,CPE 能协同增强 DOX 的细胞毒性作用,SIN 能协同增强 Cis 的细胞毒性,尤其是对 HepG2 细胞,CI<1.0:CPE SIN 顺铂 多柔比星 HCC
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