Zhao Youna, Lau Lit-Fui, Dai Xiangrong, Li Benjamin
Lee's Pharmaceutical (Hong Kong) Limited, Hong Kong,China. Email:
Asian Pac J Cancer Prev. 2016 Nov 1;17(11):4853-4856. doi: 10.22034/APJCP.2016.17.11.4853.
Objective: Gimatecan is a new camptothecin (CPT) analogue that inhibits tumor growth by targeting DNA topoisomerase I (TOP I) and introducing strong and persistent DNA cleavage. Anti-tumor activity has been demonstrated with a wide range of solid tumors in previous preclinical and clinical studies. Here, we investigated for the first time the effects of gimatecan on the proliferation of hepatocellular carcinoma (HCC) cells both in vitro and in vivo. Methods: Anticancer efficacy of gimatecan were evaluated in a panel of HCC cell lines and corresponding mouse xenograft models. Inhibition of cell proliferation was measured by CellTiter-Glo cell viability assay. In vivo, gimatecan and control preparations were orally administered every four days, for a total of four times. Tumor volume and body weights of the mice were measured twice weekly. Results: In vitro cytotoxicity evaluation showed that gimatecan inhibited the proliferation of a large panel of HCC cell lines in a dose dependent manner, with IC50 values ranging between 12.1~1085.0 nM. In vivo evaluation in mouse xenograft models showed significant antitumor effects of gimatecan at 0.8mg/kg and 0.4mg/kg as compared to the control group. Conclusion: This study suggested that gimatecan may have the potential to be used as a chemotherapeutic agent for the treatment of HCC.
吉玛替康是一种新型喜树碱(CPT)类似物,通过靶向DNA拓扑异构酶I(TOP I)并引起强烈且持久的DNA裂解来抑制肿瘤生长。在先前的临床前和临床研究中,已证明其对多种实体瘤具有抗肿瘤活性。在此,我们首次研究了吉玛替康在体外和体内对肝癌(HCC)细胞增殖的影响。方法:在一组肝癌细胞系和相应的小鼠异种移植模型中评估吉玛替康的抗癌疗效。通过CellTiter-Glo细胞活力测定法测量细胞增殖的抑制情况。在体内,每四天口服给予吉玛替康和对照制剂,共给药四次。每周两次测量小鼠的肿瘤体积和体重。结果:体外细胞毒性评估表明,吉玛替康以剂量依赖性方式抑制了一大组肝癌细胞系的增殖,IC50值在12.1~1085.0 nM之间。在小鼠异种移植模型中的体内评估表明,与对照组相比,吉玛替康在0.8mg/kg和0.4mg/kg剂量下具有显著的抗肿瘤作用。结论:本研究表明吉玛替康可能有潜力用作治疗肝癌的化疗药物。