Mao Linxi, Qin Yan, Fan Jialong, Yang Wei, Li Bin, Cao Liang, Yuan Liqin, Wang Mengyun, Liu Bin, Wang Wei
TCM and Ethnomedicine Innovation & Development International Laboratory, School of Pharmacy, Hunan University of Chinese Medicine, Changsha, 410208, China.
College of Biology, Hunan University, Changsha, 410082, China.
J Pharm Anal. 2024 May;14(5):100923. doi: 10.1016/j.jpha.2023.12.013. Epub 2023 Dec 21.
Over-expression of glutathione S-transferase (GST) can promote Cisplatin resistance in hepatocellular carcinoma (HCC) treatment. Hence, inhibiting GST is an attractive strategy to improve Cisplatin sensitivity in HCC therapy. Although several synthesized GST inhibitors have been developed, the side effects and narrow spectrum for anticancer seriously limit their clinical application. Considering the abundance of natural compounds with anticancer activity, this study developed a rapid fluorescence technique to screen "green" natural GST inhibitors with high specificity. The fluorescence assay demonstrated that schisanlactone B (hereafter abbreviated as C1) isolated from significantly down-regulated GST levels in Cisplatin-resistant HCC cells and . Importantly, C1 can selectively kill HCC cells from normal liver cells, effectively improving the therapeutic effect of Cisplatin on HCC mice by down-regulating GST expression. Considering the high GST levels in HCC patients, this compound demonstrated the high potential for sensitizing HCC therapy in clinical practice by down-regulating GST levels.
谷胱甘肽S-转移酶(GST)的过表达可促进肝细胞癌(HCC)治疗中对顺铂的耐药性。因此,抑制GST是提高HCC治疗中顺铂敏感性的一种有吸引力的策略。尽管已经开发了几种合成的GST抑制剂,但抗癌的副作用和窄谱性严重限制了它们的临床应用。考虑到具有抗癌活性的天然化合物丰富,本研究开发了一种快速荧光技术来筛选具有高特异性的“绿色”天然GST抑制剂。荧光测定表明,从 中分离出的五味子内酯B(以下简称为C1)显著下调了顺铂耐药HCC细胞中的GST水平以及 。重要的是,C1可以选择性地杀死HCC细胞而非正常肝细胞,通过下调GST表达有效提高顺铂对HCC小鼠的治疗效果。考虑到HCC患者中GST水平较高,该化合物通过下调GST水平在临床实践中显示出提高HCC治疗敏感性的巨大潜力。