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耐吉非替尼人非小细胞肺癌细胞株的建立及其耐药机制

吴敏 袁媛 潘跃银 张颖

安徽医科大学学报Issue(2):160-163,4.
安徽医科大学学报Issue(2):160-163,4.

耐吉非替尼人非小细胞肺癌细胞株的建立及其耐药机制

Establishment of a gefitinib-resistant human non-small cell lung cancer cell line and investigation of its resistance mechanism

吴敏 1袁媛 2潘跃银 3张颖1

作者信息

  • 1. 安徽医科大学第三附属医院干部病房,合肥 230061
  • 2. 合肥市滨湖医院中心实验室,合肥 230601
  • 3. 安徽医科大学第一附属医院肿瘤科,合肥 230022
  • 折叠

摘要

Abstract

Objective To establish PC9 cell line resistant to gefitinib and investigate its possible resistant mecha-nisms. Methods Human gefitinib-resistant non-small cell lung cancer cell line PC9/Gefitinib was established by gradually increasing concentration of gefitinib from its parental cell line PC9 in vitro. The IC50 value and resistance index( RI) of gefitinib were determined by MTT. MTT was also used to evaluate the sensitivity of docetaxel, peme-trexed and gemcitabine in PC9/Gefitinib cell line. Cell cycles were assayed by flow cytometry. Western blot analy-sis was used to investigate the expression of p-AKT and Bcl-2 . Results Gefitinib-resistant human non-small cell lung cancer PC9/Gefitinib had been established successfully, with the RI being 106.95. Compared to PC9 cells, PC9/Gefitinib cells had an increased sensitivity to docetaxel and showed certain resistance to pemetrexed. The cell cycles of G0/G1 period and S period had a significant difference between these two cell lines(P<0.05),the G2/M period change was not obvious. Compared with its parental PC9 cell line, the expression of Bcl-2 was significantly increased while the levels of p-AKT were obviously decreased in PC9/Gefitinib cell line. Conclusion Human ge-fitinib-resistant non-small cell lung cancer cell line PC9/Gefitinib is established successfully, and we speculate that the activation of Bcl-2 and decrease of p-AKT expression appeared to be associated with resistance to gefitinib.

关键词

吉非替尼/非小细胞肺癌/耐药

Key words

gefitinib/non-small cell lung cancer/drug-resistant

分类

医药卫生

引用本文复制引用

吴敏,袁媛,潘跃银,张颖..耐吉非替尼人非小细胞肺癌细胞株的建立及其耐药机制[J].安徽医科大学学报,2014,(2):160-163,4.

基金项目

安徽高校省级自然科学研究项目(编号:KJ2012A157) (编号:KJ2012A157)

安徽医科大学学报

OA北大核心CSTPCD

1000-1492

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