期刊文献+

乳腺癌患者外周血miRNA-134表达及化疗耐药的机制 被引量:9

Expression of peripheral blood miRNA-134 in patients with breast cancer and mechanism of chemotherapy drug resistance
下载PDF
导出
摘要 目的探讨乳腺癌患者外周血miRNA-134表达及化疗耐药的机制。方法将98例初诊乳腺癌患者根据化疗情况分为化疗敏感组(68例)和化疗耐药组(30例),采用RT-PCR检测外周血miRNA-134表达。将miRNA-mimics、miRNA-inhibitor转染至表柔比星和多西他赛耐药细胞株,检测细胞凋亡情况及Bax、Caspase-3蛋白表达水平。结果化疗敏感组血清miRNA-134表达水平明显高于化疗耐药组(P<0.05);表柔比星耐药和多西他赛耐药细胞增殖能力明显低于MCF-7细胞(P<0.05)。与正常MCF-7细胞系比较,表柔比星耐药细胞系、多西他赛耐药细胞系miRNA-134表达水平均明显降低(P<0.05)。转染miRNA-mimics细胞凋亡率明显高于未转染细胞和细胞miRNA-inhibitor细胞(P<0.05)。转染miRNA-mimics细胞Bax、Caspase-3蛋白表达水平明显高于未转染细胞和转染miRNA-inhibitor细胞(P<0.05)。结论 miRNA-134可能通过促进Bax、Caspase-3的表达,增强乳腺癌细胞对化疗的敏感性。 Objective To explore the expression of peripheral blood miRNA-134 in the patients with breast cancer and chem- otherapy drug resistance mechanism. Methods A total of 98 cases of newly diagnosed breast cancer were divided into the chemo- therapy sensitive group(n= 58) and chemotherapy drug resistant group(n=30). The expression of miRNA-134 in peripheral blood was measured by adopting RT-PCR. miRNA-mimics and miRNA-inhibitor were transfeeted into epirubiein and docetaxel resistant cell lines, the cell apoptosis and expression levels of Bax and Caspase-3 protein were detected. Results The ievel of serum!haiRNA- 134 expression in the chemotherapy sensitive group was significantly higher than that in the chemotherapy drug resistant group (P〈0.05) ;the proliferation capacity of epirubicin and docetaxel resistant cell lines was significantly lower than that in the MCF-7 cells (P〈0, 05). Compared with normal MCF-7 cell line, the expression level of miRNA-134 in the epirubicin and docetaxel resistant cell lines was significantly decreased(P〈0.05). The apoptosis rate in the miRNA-mimics group was significantly higher than that in the control group and miRNA-inhibitor group(P〈0.05). The expression of Bax and Caspase-3 protein in the miRNA-mimics group was significantly higher than that in the control group and miRNA-inhibitor group(P〈0.05). Conclusion MiRNA-134 may enhance the sensitivity of breast cancer cells to chemotherapy by promoting the expression of Bax and Caspase-3.
出处 《重庆医学》 CAS 2018年第6期779-782,785,共5页 Chongqing medicine
关键词 乳腺肿瘤 新辅助化疗 耐药 微RNA-134 作用机制 breast neoplasms neoadjuvant chemotherapy drug resistance micro RNA-134 mechanism
  • 相关文献

参考文献5

二级参考文献28

  • 1Ming Gao,Hao Yin,Zhe-Wei Fei.Clinical application of microRNA in gastric cancer in Eastern Asian area[J].World Journal of Gastroenterology,2013,19(13):2019-2027. 被引量:16
  • 2Creighton CJ,Li X,Landis M,et al.Residual breast cancers after conventional therapy display mesenchymal as well as tumor-initiating features[J] .PNAS,2009,106(33) :13820-13825.
  • 3Wind NS, Holen I. Multidrug resistance in breast cancer:from in vitro models to clinical studies[J] . Int J Breast Cancer,2011,2011:967419.
  • 4Dontu G,Abdallah WM. In vitro propagation and transcriptional profiling of human mammary stem/progenitor cells[J] .Genes Dev,2003,17(10) :1253-1270.
  • 5Wang Z,Li Y,Ahmad A,et al.Targeting miRNAs involved in cancer stem cell and EMT regulation:an emerging concept in overcoming drug resistance[J] .Drug Resist Updat,2010,13(4-5) :109-118.
  • 6Creighton CJ,Chang JC,Rosen JM.Epithelial-mesenchymal transition(EMT) in tumor-initiating cells and its clinical implications in breast cancer[J] .J Mammary Gland Biol Neoplasia,2010,15(2) :253-260.
  • 7Singh A,Settleman J.EMT,cancer stem cells and drug resistance:an emerging axis of evil in the war on cancer[J] .Oncogene,2010,29(34) :4741-4751.
  • 8Tajima H,Ohta T,Kitagawa H,et al.Neoadjuvant chemotherapy with gemcitabine for pancreatic cancer increases in situ expression of the apoptosis marker M30 and stem cell marker CD44[J] .Oncol Lett,2012,3(6) :1186-1190.
  • 9Bertolini G,Roz L,Perego P,et al.Highly tumorigenic lung cancer CD133+ cells display stem-like features and are spared by cisplatin treatment[J] .PNAS,2009,106(38) :16281-16286.
  • 10Alvero AB,Chen R,Fu HH,et al.Molecular phenotyping of human ovarian cancer stem cells unravel the mechanisms for repair and chemo-resistance[J] .Cell Cycle,2009,8(1) :158-166.

共引文献49

同被引文献93

引证文献9

二级引证文献37

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部