引用本文:吴 爽 1,张 阳 2,李 斌 1,范丽昕 3.伊立替康节拍式化疗联合索拉非尼对人肝癌细胞HepG2及内皮细胞HUVECs的抑制作用[J].大连医科大学学报,2015,37(5):429-431.
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伊立替康节拍式化疗联合索拉非尼对人肝癌细胞HepG2及内皮细胞HUVECs的抑制作用
吴 爽 1,张 阳 2,李 斌 1,范丽昕 31,2,3
1.大连市友谊医院 肿瘤内科,辽宁 大连 116001;2.大连医科大学附属第二医院 肿瘤内科,辽宁 大连 116027;3.大连市第三人民医院 肿瘤内科,辽宁 大连 116091
摘要:
[摘要] 目的 观察伊立替康(CPT-11)节拍式化疗联合索拉非尼(Sorafenib)对人肝癌细胞HepG2生长的影响及对血管内皮细胞的抑制作用。 方法 取对数生长的HepG2细胞、人脐静脉内皮细胞(HUVECs)培养后分组给药:(1)对照组,加培养液。(2)索拉非尼组,6 μmol/L。(3)CPT-11(LDM)组,CPT-11 30 μg/mL。(4)CPT-11(TDM)组,CPT-11 160 μg/mL。(5)CPT-11(LDM)30 μg/mL +索拉非尼 6 μmol/L组。用MTT法检测各实验组人HepG2细胞及HUVECs细胞培养24 h、48 h、72 h后的平均OD值,计算抑制率。 结果 CPT-11(LDM)组对HepG2细胞抑制作用不明显,明显低于其他实验组(P<0.05)。 CPT-11(LDM)与索拉非尼联合用药对HUVECs细胞的抑制作用最明显,显著高于单独用药(P<0.05)。 结论 小剂量伊立替康(CPT-11)体外能够抑制内皮细胞增殖,但对肿瘤细胞HepG2抑制作用有限。靶向治疗联合节拍式化疗效果更佳。
关键词:  HepG2细胞  人脐静脉内皮细胞  索拉非尼  伊立替康  节拍式化疗
DOI:10.11724/jdmu.2015.05.04
分类号:
基金项目:基金项目:大连市卫生局课题基金项目(2012)
Effects of metronomic irinotecan chemotherpy combined with Sorafenib on human hepatocellular carcinoma strain HepG2 and human umbilical vascular endothelial cells HUVECs
WU Shuang 1, ZHANG Yang 2,LI Bin 1, FAN Li-xin 31,2,3
1.Department of Oncology, The Friendship Hospital of Dalian,Dalian 116001, China;2. Department of Oncology, the Second Affiliated Hospital of Dalian Medical University, Dalian 116027, China;3.Department of Oncology, The Third Hospital of Dalian, Dalian 116091, China
Abstract:
[Abstract] Objective To observe the inhibition effect of low dose CPT-11 combined with Sorafenib on the growth of human heptatic carcinoma strain HepG2 and the proliferation of human umbilical vascular endothelial cells (HUVECs). Methods HUVECs and HepG2 cells were divided into 5 groups: control group, Sorafenib-treated group 6 μmol/L, CPT-11(LDM)- treated group 30 μg/mL, CPT-11(TDM)- treated group 160 μg/mL and Sorafenib+ CPT-11(LDM)-treated group. The cell proliferation inhibition rate was calculated with MTT assays. Results Both Sorafenib and Low dose CPT-11 can inhibit the proliferation of HUVECs, and the inhibition rate in group sorafenib+CPT-11(LDM) treated group higher than that in sorafenib group and CPT-11(LDM) group (P<0.05). LDM chemotherapy had little inhibition effect on HepG2. The inhibition rate to HepG2 in CPT-11(LDM) group was significantly lower than that in others group (P<0.05). Conclusion The anti-tumour effects of Low-dose CPT-11 could be from its angiogenesis inhibition. The combination of Sorafenib and CPT-11(LDM) would be a better choice.
Key words:  [Key words] hepatic carcinoma strain HepG2  human umbilical vascular endothelial cells  Sorafenib  irinotecan  metronomic chemotherapy