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下调miR-214对鼻咽癌CNE2细胞凋亡的影响 被引量:4

Effects of Down-Regulation of miR-214 on the Apoptosis of CNE2 Cell in Nasopharyngeal Carcinoma
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摘要 目的:研究miR-214对鼻咽癌细胞CNE2凋亡的影响及机制。方法:RT-PCR检测鼻咽癌细胞CNE2和正常鼻咽上皮细胞NP69细胞中miR-214的表达;通过miR-214inhibitor转染鼻咽癌细胞CNE2,流式细胞仪(FCM)检测鼻咽癌细胞凋亡变化;并用Western印迹法检测细胞中Bcl-2和Bax蛋白的表达变化。结果:正常鼻咽上皮细胞明低表达miR-214,而鼻咽癌CNE2细胞中明显高表达miR-214(P<0.05),miR-214inhibitor可浓度依赖性的抑制miR-214的表达(P<0.05)。40μmol/L和5μmol/L的miR-214inhibitor组细胞凋亡率分别为:(45.3±9.1)%和(12.3±3.8)%,而NC inhibitor组细胞的凋亡率为(5.1±0.4)%。miR-214inhibitor可下调Bcl-2的表达(P<0.05),对Bax的表达无明显影响。结论:miR-214可能通过下调Bcl-2的表达从而诱导CNE2细胞凋亡,这可能为鼻咽癌的治疗提供新靶点。 Objective:To investigate the effect of MicroRNA-214(miR-214)on apoptosis of nasopharyngeal carcinoma cell line CNE2.Methods:miR-214 in vitro was transiently transferred into nasopharyngeal carcinoma cell line CNE2.The expression level of miR-214 in CNE2cells and nasopharyngeal epithelial cell line NP69 was detected by real-time fluorescence quantitative PCR.Apoptosis was analyzed by flow cytometry.Expression of Bcl-2and Bax protein was detected by Western blot.Results:miR-214 in nasopharyngeal carcinoma cell line CNE2 was significantly increased compared with nasopharyngeal epithelial cell line NP69(P〈0.05).The apoptosis rate of40μmol/L miR-214 inhibitor group,5μmol/L miR-214 inhibitor group and NC inhibitor group were(45.3±9.1)%,(12.32±3.8)%and(5.12±0.4)%,respectively.The difference was significant statistically(P〈0.05).And the expression levels of Bcl-2were markedly down-regulated by miR-214inhibitor(P〈0.05).Conclusion:The miR-214down-regulated Bcl-2induces apoptosis in nasopharyngeal carcinoma cells,which provids a new target for the treatment of nasopharyngeal carcinoma.
出处 《武汉大学学报(医学版)》 CAS 北大核心 2014年第6期848-851,共4页 Medical Journal of Wuhan University
关键词 鼻咽癌 凋亡 非编码小RNA 转染 流式细胞检测 Nasopharyngeal Carcinoma Apoptosis MicroRNA Transfection Flow Cytometry
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参考文献10

  • 1Jia WH, Qin HD. Non-viral environmental risk factors for nasopharyngeal carcinoma a systematic review[J]. Semin Cancer, Biol,2012,22(2) :117-126.
  • 2He ML, Luo MX, Lin MC,et al. Micro RNAs: poten- tial diagnostic markers and therapeutic targets for EBV- associated nasopharyngeal carcinoma[J]. Biochim Bio- phys Acta,2012, 825(1) :1-10.
  • 3Nishimura Y, Komatsu S, Ichikawa D, et at. Overex- pression of YWHAZ relates to tumor cell proliferation and malignant outcome of gastric carcinoma[J]. Br J Cancer, 2013,108(6):1 324-1 331.
  • 4Yin G, Chen R, Alvero AB, et al. TWISTing stem- hess, inflammation and proliferation of epithelial ovari- an cancer cells through MIR199A2/214[J]. Oncogene, 2010,29(24) :3 545-3 553.
  • 5Penna E, Orso F, Cimino D, et al. microRNA-214 contributes to melanoma turnout progression through suppression ofTFAP2C[J]. EMBO J, 2011,30(10): 1 990-2 007.
  • 6Zhang XJ, Ye H, Zeng CW, et al. Dysregulation of miR-15a and miR-214 in human pancreatic cancer[J]. J Hematol Oncol, 2010,3(23) :46-52.
  • 7林述琨,王耀鹏,温吉海.miR-214对人肺癌A549细胞增殖和侵袭能力的影响[J].药品评价,2012,9(36):31-34. 被引量:2
  • 8Yu ZW, Zhong LP, Ji T,et al. MicroRNAs contribute to the chemoresistance of cisplatin in tongue squamous cell carcinoma lines[J]. Oral Oncol, 2010,46(4) :317- 322.
  • 9Peng RQ, Wan HY, Li HF, et al. MicroRNA-214 suppresses growth and invasiveness of cervical cancer cells by targeting UDP-N-acetyl-a-D-galactosamine: polypeptide N-acetylgalactosaminyltransferase [ J ]. J Biol Chem, 2012,287(17):1 4 301-14 309.
  • 10Dicou E, Perez-Polo JR. Bax-an emerging role in ectop- ic cell death[J]. Int J Dev Neurosci, 2009,27(4):299- 304.

二级参考文献11

  • 1Hiyoshi Y, Kamohara H,Karashima R,et al.MicroRNA-21 regulates the proliferation and invasion in esophageal squamous cell carcinoma[J]. Clin Cancer Res,2009,15 (6): 1915-1922.
  • 2Barte! DP.MicroRNAs:genomics,biogenesis,mechanism and function[J] .Ce11,2004,16(2) :281-297.
  • 3Agrawal R,Tran U,Wessely O.The miR-30 miRNA family regulates Xenopus pronephros development and targets the transcription factor Xlim 1/Lhxl [J].Development,2009,136(23):3927-3936.
  • 4Venugopal SK,Jiang J,Kim TH,et al.Liver fibrosis causesdownregulation of miRNA-150 and miRNA-194 in hepatic stellate cells and their overexpression causes decreased stellate cell activation[J].Physiol Gastrointest Liver Physiol,2010,298(1):G101-106.
  • 5Osada H,Takahashi T.MicroRNAs in biological processes and carcinogenesis[J].Carcinogenesis,2007,28(1):2-12.
  • 6C.C.Wong,C.M.Wong,E.K.Tung,et al.The microRNA miR- 139 suppresses metastasis and progression of hepatocellular carcinoma by down-regulating Rho-kinase 2[J].Gastroenterolo gy,2011,140(1):322-331.
  • 7Wang Y, Lee AT,Ma JZ,et al.Profiling microRNA expression in hepatocellular carcinoma reveals microRNA-224 up-regulation and apoptosis inhibitor-5 as a microRNA-224-specific target[J].J Biol Chem,2008,283 (19):13205-13215.
  • 8Yang Z,Chen S,Luan X,et aI.MicroRNA-214 is aberrantly expressed in cervical cancers and inhibits the growth of HeLa cells[J].IUBMB Life,2009,61 (11): 1075 1082.
  • 9Derfoul A,Juan AH,Difilippantonio MJ,et al.Decreased microRNA-214 levels in breast cancer cells coincides with increased cell proliferation,invasion and accumulation of the Polycomb Ezh2 methyltransferase[J].Carcinogenesis,2011,32 ( 1 l ): 1607-1614.
  • 10SCHRATT GM,TUEBING F,NIGH EA,et al.A brain- specific microRNA regulates dendritic spine development[J]. Nature,2006,439(7074):283 -289.

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