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吉非替尼联合紫杉醇对食管癌细胞体内外生长抑制实验研究
引用本文:卢红,王建军,周芳,程传耀.吉非替尼联合紫杉醇对食管癌细胞体内外生长抑制实验研究[J].肿瘤防治杂志,2014(17):1334-1338.
作者姓名:卢红  王建军  周芳  程传耀
作者单位:河南大学淮河医院肿瘤科,河南开封475000
基金项目:河南省科技厅重点攻关项目(112102310090)
摘    要:目的:探讨吉非替尼联合紫杉醇对人食管癌细胞株Eta-109在体内外生长的影响及其可能机制。方法:按两因素析因设计试验,并应用MTT法观察单用吉非替尼、紫杉醇及联合应用对Eca-109细胞增殖的抑制作用,流式细胞术检测细胞周期和凋亡。按单因素影响设计,建立裸鼠人食管癌皮下移植瘤模型,并分为4组各10只,分别为对照组、紫杉醇组、吉非替尼组及吉非替尼+紫杉醇联合组。经过不同处理4周后,切除瘤灶,称瘤质量,计算抑瘤率。结果:MTT法结果显示,药物干预72h后,各用药组与对照组比较,吸光度A值均减小,吉非替尼作用72h的半数抑制浓度为(1.72±0.27)μmol/L,紫杉醇的半数抑制浓度为(5.27±0.88)μmol/L。流式细胞术检测结果显示,4组G0/G1、S和G2/M期细胞比较差异均有统计学意义,P〈0.05;对照组Eca-109细胞的凋亡率为(9.69±1.42)%,紫杉醇组为(12.41±2.75)%,吉非替尼组为(22.0±4.26)%,吉非替尼+紫杉醇联合组为(33.1±3.78)%,差异有统计学意义,P〈0.001。对照组肿瘤体积为(1.56±0.16)cm3,紫杉醇组为(0.81±0.15)cm3,吉非替尼组为(1.35±0.08)cm3,紫杉醇+吉非替尼联合组为(O.54±0.11)cm3,差异有统计学意义,P<0.05。结论:吉非替尼与紫杉醇合用对体内外食管癌Eta-109细胞具有显著的抑制作用,且强于药物单一作用。

关 键 词:吉非替尼  紫杉醇  食管癌细胞  抑制作用

Experimental study on growth inhibition of Gefitinid combined with paclitaxel on esophageal carcinoma cells in vitro and in vivo
LU Hong,WANG J ian-jun,ZHOU Fang,CHENG Chuan-yao.Experimental study on growth inhibition of Gefitinid combined with paclitaxel on esophageal carcinoma cells in vitro and in vivo[J].China Journal of Cancer Prevention and Treatment,2014(17):1334-1338.
Authors:LU Hong  WANG J ian-jun  ZHOU Fang  CHENG Chuan-yao
Affiliation:( Department of Oncology , Henan University Huaihe Hospital ,Kai f eng 475000 ,P. R. China)
Abstract:OBJECTIVE:To observe the effect of gefitinib combined with paclitaxel on proliferation of human esopha- geal cancer cell line Eca-109 in vitro and in vivo ,and explore its possible mechanism. METHODS: By two-factor factorial design trial, MTT was used to observe gefitinib, paclitaxel alone and in combination with inhibitory effects on Eca-109 cell proliferation. FCM was used to detect cell cycle profile and apoptotic rate of Eca-109. Also designed by a single factor, to establish the transplant tumor model of human esophageal carcinoma in nude mice subcutaneously, 40 mice were randomly divided into four groups : control group, paelitaxeI group, gefitinib group, gefitinib combined with paciitaxe group, 4 weeks later the tumor were resected and tumor weight and inhibitory rate were calculated. RESULTS: After drug intervention 72 h,A values were decreased in all groups (P=0.01) ;ICs0 of gefitinib group was (1.72±0.27) μmol/L;IC50 of paclitax- el group was (5.27±0.88) μmol/L;FCM analysis showed that the differences among the four groups of Go/G1 phase, S phase,G2/M phase cells were statistically significant; In control group, PTX group, Gefitinib group and PTX+ Gefitinib group, the apoptosis rate of Eca-109 cells respectively were (9.69 ± 1.42) %, ( 12.41 ± 2. 75) %, (22.0 ± 4. 26) % and (33.1±3. 78)%, the differences were statistically significant (P〈 0. 001). The tumor volume in control group, PTX group,Gefitinib group and PTX+ Gefitinib group were (1. 56 ± 0. 16) cm3 , (0. 81 ± 0. 15) cm3 , (1. 35 ± 0. 08) cm3 , (0.54 ± 0.11) cm3 , and the differences were statistically significant (P〈 0.05). CONCLUSION : Gefitinib combined with paclitaxel has a significant inhibitory effect on Eca-109,and the effect is better than that with single drug.
Keywords:Gefitinib  Paelitaxel  esophageal carcinoma  inhibitory effect
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