摘要
目的:研究全反式维甲酸联合奥沙利铂对结肠癌LoVo细胞株增殖、血管新生能力的影响。方法:培养结肠癌LoVo细胞株,分为空白对照组(不含FBS的培养基处理)、ATRA组(10-5 mol/L全反式维甲酸处理)、OHP组(80μg/mL奥沙利铂处理)、联合处理组(10-5 mol/L全反式维甲酸和80μg/mL奥沙利铂共同处理)。采用MTT法检测细胞增殖能力,real-time PCR检测血管新生因子的mRNA含量,酶联免疫吸附法检测血管新生因子的蛋白含量。结果:(1)细胞增殖能力:联合处理组、ATRA组、OHP组的MTT值均低于空白对照组(P<0.05),且联合处理组的MTT值低于ATRA组、OHP组(P<0.05);(2)血管新生因子:联合处理组、ATRA组、OHP组的血管内皮生长因子(VEGF)A、VEGFB、VEGFC、转化生长因子(TGF)β1、缺氧诱导因子(HIF)-1α的表达量均低于空白对照组,且联合处理组的VEGFA、VEGFB、VEGFC、TGFβ1、HIF-1α的表达量低于ATRA组、OHP组(P<0.05)。结论:全反式维甲酸联合奥沙利铂能够抑制结肠癌LoVo细胞株的增殖,降低血管新生因子的表达。
Objective: To study the effects of all trans retinoic acid combined with oxaliplatin on proliferation and angio- genesis ability of colorectai cancer LoVo cell line. Methods~ Colorectal cancer LoVo cell line were cultured and divided into blank control group(treated with culture medium without FBS), ATRA group(treated with 10^-5 mol/L all trans retinoic acidt), OHP group (treated with 80/zg/mL oxaliplatin), combination group(treated with 10 5 mol/L all trans retinoic acidt and 80 μg/ mL oxaliplatin). Cell proliferation was detected by MTT method, mRNA content of angiogenesis factor were detected by real- time PCR, protein content of angiogenesis factor were detected by enzyme linked immunosorbent assay. Results: MTT values of combined treatment group, ATRA group, OHP group were lower than those of blank control group; MTT values of ATRAgroup, OHP group were lower than combined treatment group. VEGFA, VEGFB, VEGFC, TGFβ1, HIF-1α expression of combined treatment group, ATRA group, OHP group were lower than those of blank control group; VEGFA, VEGFB, VEGFC, TGFβ1, HIF-1α expression of ATRA group, OHP group were lower than those of combined treatment group. Conclusion: All trans retinoic acid combined with oxaliplatin treatment can inhibit the proliferation of colon cancer cell line LoVo and reduce the expression of angiogenesis factors.
出处
《海南医学院学报》
CAS
2014年第12期1610-1613,共4页
Journal of Hainan Medical University
基金
恩施土家族苗族自治州科技局重点项目(201012)~~
关键词
结肠癌
全反式维甲酸
奥沙利铂
增殖
血管新生
Colon cancer
All trans retinoic acid
Oxaliplatin
Proliferation
Angiogenesis