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耐吉非替尼的HCC827 GR细胞的高效诱导及其药理学特性

钟磊 师健友

中国药理学通报2016,Vol.32Issue(9):1284-1288,5.
中国药理学通报2016,Vol.32Issue(9):1284-1288,5.DOI:10.3969/j.issn.1001-1978.2016.09.019

耐吉非替尼的HCC827 GR细胞的高效诱导及其药理学特性

Efficient induction of gefitinib-resistant cell line HCC827 GR and its pharmacological properties

钟磊 1师健友1

作者信息

  • 1. 电子科技大学附属医院,四川省人民医院,个体化药物治疗四川省重点实验室,四川 成都 610072
  • 折叠

摘要

Abstract

Aim To establish a gefitinib-resistant NSCLC cell line, and observe its pharmacological properties. Methods HCC827 cells were treated with hepatocyte growth factor( HGF) and increasing concen-tration of gefitinib to induce cell resistance. MTT assay was used to test cell viability and chemosensitivity. Clone formation and Edu staining were used to verify the inhibitory effect of gefitinib on cell growth. qRT-PCR and Western blot were used to assay the expres-sion of c-Met. Results The use of HGF greatly short-ened the induction time of HCC827GR resistant cells. gefitinib could significantly suppress cell viability, col-ony formation and cell proliferation of HCC827 , but had a weaker inhibitory effect on HCC827GR cells. HCC827GR overexpressed c-Met protein, and was highly sensitive to c-Met inhibitors. Conclusion The gefitinib-resistant HCC827 GR cells were induced suc-cessfully and efficiently. The growth of HCC827GR is dependent on the activity of c-Met protein, and it can be used as a phenotypic screening model of c-Met in-hibitors.

关键词

非小细胞肺癌/吉非替尼/c-Met/耐药/表型筛选/激酶抑制剂

Key words

non-small cell lung cancer/gefitinib/Met/drug resistance/phenotypic screening/kinase inhibitor

分类

医药卫生

引用本文复制引用

钟磊,师健友..耐吉非替尼的HCC827 GR细胞的高效诱导及其药理学特性[J].中国药理学通报,2016,32(9):1284-1288,5.

基金项目

国家自然科学基金资助项目(No 81302643) (No 81302643)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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