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微小RNA-218在胃癌中的表达与作用 被引量:6

Reduced expression of miR-218 and its significance in gastric cancer
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摘要 目的检测微小RNA-218(miR-218)在胃癌组织中的表达水平及其功能,探讨miR-218在胃癌发生、发展中的作用和意义。方法采用发夹状引物的逆转录聚合酶链反应(RT—PCR)技术,检测20例非贲门胃癌组织和正常胃黏膜组织中miR-218的表达水平。通过转染不同的外源性分子,改变胃上皮AGS细胞miR-218的表达水平,检测miR-218对细胞增殖、凋亡、细胞周期和侵袭能力的影响。结果与正常胃黏膜组织相比,miR-218在胃癌组织中呈低表达(P〈0.01),其比值平均为0.19(范围0.01~0.70)。流式细胞技术检测结果显示,转染miR-218前体的AGS细胞凋亡率(21.6%)明显增加,与转染阴性参照(10.4%)的AGS细胞差异有统计学意义(P〈0.05)。与转染阴性参照比较,转染miR-218前体可明显抑制细胞增殖(P〈0.01)。Transwell试验证实,AGS细胞在转染miR-218前体后,细胞侵袭能力明显减弱(P〈0.05)。结论在胃癌组织中,miR-218的表达降低,miR-218具有促进细胞凋亡、抑制细胞增殖和侵袭的功能。 Objective To investigate the expression and function of miR-218 in gastric cancer. Methods miR-218 levels were evaluated in 20 non-cardia gastric cancer tissues using TaqMan stem-loop real-time PCR analysis. Prc-miR-218 and anti-miR-218 inhibitor were used to change the miR-218 expression level and examine its effects on cell proliferation, apoptosis, cell cycle and cell invasion. Results Comparing with the corresponding normal tissues, miR-218 expression was significantly reduced in the gastric cancer tissue (P 〈0.01 ). Forced expression of miR-218 increased apoptosis in AGS cells. The proportion of apoptosis cells induced by transfection of pre-miR-218 was greater than that induced by control (21.6% vs. 10.4% , P =0. 032). Pre-miR-218 resulted in a significantly decreased cell growth activity (P 〈0.01 ) and cell invasion ( P 〈 0.05) of AGS cells compared with that of the control. Conclusion miR-218 expression is reduced in gastric cancer, miR-218 may function as a tumor suppressor in gastric carcinoma.
出处 《中华肿瘤杂志》 CAS CSCD 北大核心 2010年第4期249-252,共4页 Chinese Journal of Oncology
基金 高等学校博士学科点专项科研基金 国家自然科学基金(30670940、30770112)
关键词 胃肿瘤 MIR-218 细胞增殖 细胞凋亡 Stomach neoplasms miR-218 Cell proliferation Cell apoptosis
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  • 1Lewis BP,Burge CB,Bartel DP,et al.Conserved seed pairing,often flanked by adenosines,indicates that thousands of humangenes are microRNA targets.Cell,2005,120:15-20.
  • 2Cho WC.OncomiRs:the discovery and progress of microRNAs in cancers.Mol Cancer,2007,6:60.
  • 3Liu T,Tang H,Lang Y,et al.MicroRNA-27a functions as an oncogene in gastric adenocarcinoma by targeting prohibitin.Cancer Lett,2008,273:233-242.
  • 4Zhang Z,Li Z,Gao C,et al.miR-21 plays a pivotal role in gastric cancer pathogenesis and progression.Lab Invest,2008,88:1358-1366.
  • 5Chan JA,Krichevsky AM,Kosik KS.MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells.Cancer Res,2005,65:6029-6033.
  • 6Si ML,Zhu S,Wu H,et al.miR-21-mediated tumor growth.Oncogene,2007,26:2799-2803.
  • 7Petrocca F,Visone R,Onelli MR,et al.E2Fl-regulated microRNAs impair TGFbeta-dependent cell-cycle arrest and apoptosis in gastric cancer.Cancer Cell,2008,13:272-286.
  • 8Volinia S,Calin GA,Liu CG,et al.A microRNA expression signature of human solid tumors defines cancer gene targets.Proc Natl Acad Sci U S A,2006,103:2257-2261.
  • 9Cheng AM,Byrom MW,Shelton J,et al.Antisense inhibition of human miRNAs and indications for an involvement of miRNA in cell growth and apoptosis.Nucleic Acids Res,2005,33:1290-1297.
  • 10Martinez I,Gardiner AS,Board KF,et al.Human papillomavirus type 16 reduces the expression of microRNA-218 in cervical carcinoma cells.Oncogene,2008,27:2575-2582.

同被引文献52

  • 1Si-Biao Su,Shan-Yu Qin,Xiao-Yun Guo,Wei Luo,Hai-Xing Jiang.Assessment by meta-analysis of interferon-gamma for the diagnosis of tuberculous peritonitis[J].World Journal of Gastroenterology,2013,19(10):1645-1651. 被引量:17
  • 2李招权,魏明竟.微RNA在肿瘤研究中的意义[J].重庆医学,2006,35(19):1803-1806. 被引量:5
  • 3Lagos-Quintana M, Rauhut R, Lendeckel W, et al. Identification of novel genes coding for small expressed RNAs. Science, 2001, 294 : 853-858.
  • 4Lau NC, Lim LP, Weinstein EG, et al. An abundant class of tiny RNAs with probable regulatory roles in Caenorhabditis elegans. Science, 2001, 294:858-862.
  • 5Lee RC, Ambros V. An extensive class of small RNAs in CaenodmtMitis elegans. Science, 2001, 294:862-864.
  • 6Hwang HW, Mendell JT. MicroRNAs in cell proliferation, cell death, and tumorigenesis. Br J Cancer, 2006, 94:776-780.
  • 7Calin GA, Sevignani C, Dumitru CD, et al. Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers. Proc Natl Acad Sci U S A, 2004, 101:2999- 3004.
  • 8Lu J, Getz G, Miska EA, et al. MicroRNA expression profiles classify human cancers. Nature, 2005, 435:834-838.
  • 9Goparaju CM, Blasberg JD, Volinia S, et al. Onconase mediated NFKβ downregulation in malignant pleural mesothelioma. Oncogene, 2011, 30:2767-2777.
  • 10Busacca S, Germano S, De Cecco L, et al. MicroRNA signature of malignant mesothelioma with potential diagnostic and prognostic implications. Am J Respir Cell Mol Biol, 2010, 42:312-319.

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