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非小细胞肺癌中EGFR突变与雌激素受体表达的相关性研究
  • ISSN号:1671-8348
  • 期刊名称:重庆医学
  • 时间:2015
  • 页码:2881-2886
  • 分类:R734.2[医药卫生—肿瘤;医药卫生—临床医学]
  • 作者机构:[1]郑州大学附属肿瘤医院消化内科,郑州450008, [2]郑州大学附属肿瘤医院普外科,郑州450008, [3]郑州大学附属肿瘤医院胸外科,郑州450008
  • 相关基金:国家自然科学基金面上资助项目(81172240)
  • 相关项目:靶向notch基因的microRNA分子鉴定及其抗肺癌细胞增殖和迁移研究
中文摘要:

目的探讨miR-374a和miR-548调控非小细胞肺癌对吉非替尼耐药的机制。方法 ①qRT-PCR检测转染载体miR-Zip-347a或p-miR-548b的HCC827-Gef和Calul细胞中miR-374a或miR-548b的相对表达水平;并检测转染pcDNA-Wnt5a和pcDNA-CCNB1及其对照载体的HCC827-Gef细胞中Wnt5a和CCNB1的相对表达水平。②MTS法检测敲除miR-374a或过表达miR-548b的HCC827-Gef和Calul细胞对吉非替尼的敏感性,并分析过表达蛋白Wnt5a或CCNB1的HCC827-Gef细胞对吉非替尼的敏感性;③荧光素酶报告基因检测共转染相应载体后的HEK293细胞中荧光素酶活性。④蛋白印迹分析转染p-miR-374a、p-miR-548b和p-miR-control的细胞中Wnt5a或CCNB1的表达水平。结果 ①非小细胞肺癌细胞Calul和HCC827-Gef中miR-374a表达明显受到抑制或miR-548b过表达时,其对吉非替尼的敏感性显著升高;2HCC827-Gef细胞miR-374a和miR-548b过表达分别显著降低Wnt5a和CCNB1蛋白的表达;HCC827-Gef细胞中Wnt5a过表达可部分逆转非小细胞肺癌细胞对吉非替尼的耐药;转染p-miR-548b的HCC827-Gef细胞中CCNB1的再表达也说明了细胞对吉非替尼的敏感性。结论 miR-374a和miR-548b分别通过靶向Wnt5a和CCNB1基因调控非小细胞肺癌细胞对吉非替尼的敏感性。

英文摘要:

Objective To investigate the mechanism of miR-374 a and miR-548 in the regulation of non-small cell lung cancer to gefitinib resistance. Methods ①The expression of miR-374 a and miR-548 b in HCC827-Gef and Calul cells transfected with miR-Zip-374 a or p-miR-548 b were detected by qRT-PCR. And the expression levels of CCNB1 and Wnt5 a in HCC827-Gef cells transfected with pcDNA-Wnt5 a,pcDNA-CCNB1 and their control vectors were also detected by qRT-PCR. ②MTS assay was used to detect the sensitivity of HCC827-Gef and Calul cells knocked down of miR-374 a or overexpressed of miR-548 b to gefitinib. And the sensitivity of HCC827-Gef was also detected by MTS when protein Wnt5 a or CCNB1 were overexpressed. ③Luciferase reporter assay was used to detect the luciferase activity of HEK293 cells after co-transfected with corresponding vector. ④Western blot was used to analyze the expression levels of Wnt5 a or CCNB1 in cells transfected with p-miR-374 a,p-miR-548 b and p-miR-control. Results ①When the expression of miR-374 a was significantly inhibited or miR-548 b overexpressed in Calul and HCC827-Gef cells,their sensitivity to gefitinib was increased. ②Overexpression of miR-374 a and miR-548 b in HCC827-Gef cells separately reduced the expression of Wnt5 a and CCNB1 protein; And the overexpression of Wnt5 a in HCC827-Gef cells could partly reverse the drug resistance of non-small cell lung cancer cells to gefitinib; In the same way,the re-expression of CCNB1 in HCC827-Gef cells transfected with p-miR-548 b also showed the sensitivity of the cells to gefitinib. Conclusion MiR-374 a and miR-548 b regulate the sensitivity of non-small cell lung cancer to gefitinib respectively by targeting Wnt5 a and CCNB1 genes.

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期刊信息
  • 《重庆医学》
  • 北大核心期刊(2011版)
  • 主管单位:重庆市卫生和计划生育委员会
  • 主办单位:重庆市卫生信息中心
  • 主编:吴开明
  • 地址:重庆市渝北区回兴唐家沟宝环路420号
  • 邮编:401120
  • 邮箱:
  • 电话:023-61965157
  • 国际标准刊号:ISSN:1671-8348
  • 国内统一刊号:ISSN:50-1097/R
  • 邮发代号:78-27
  • 获奖情况:
  • “中国科技论文在线”2011年“一等奖”,2012年重庆市新闻出版局“重庆报刊发展专项基金”
  • 国内外数据库收录:
  • 美国化学文摘(网络版),英国农业与生物科学研究中心文摘,波兰哥白尼索引,美国剑桥科学文摘,中国中国科技核心期刊,中国北大核心期刊(2008版),中国北大核心期刊(2011版),中国北大核心期刊(2014版)
  • 被引量:91150