期刊文献+

miR-200家族作为卵巢癌预后标志物的meta分析 被引量:3

Prognostic Role of mi R-200 Family in Ovarian Cancer: a Meta-analysis
原文传递
导出
摘要 目的:系统评价mi R-200家族(mi R-200a、mi R-200b、mi R-200c、mi R-141、mi R-429)的表达与卵巢癌预后之间的关系。方法:仔细检索搜索美国国立图书馆(Pub Med),荷兰医学文摘(EMBASE)以及ISI Web of Science、CNKI、万方等数据库,与mi R-200家族相关的卵巢癌预后的文献。检索日期为数据库的建库时间至2013年9月20日。提取与mi R-200家族相关卵巢癌预后的相应数据,应用Stata11.0软件进行Meta分析。结果:共有7篇研究符合入选标准,累积肿瘤组织577例。Meta分析显示,mi R-200家族低表达组的合并优势比是高表达组的1.347倍(95%CI:1.052,1.725)。mi R-200a、mi R-200c、mi R-141的亚组分析结果分别为1.091(95%CI:0.718,1.659)、1.285(95%CI:0.765,2.161),1.122(95%CI:1.043-1.208)。mi R-200家族、mi R-141与卵巢癌的预后之间的关系有统计学意义(P=0.018,P=0.002)。结论:mi R-200家族在卵巢癌的预后判断中可能起到预后标记物的作用。 Objective: To systemically evaluate the relationship between miR-200 family and the prognosis of ovarian cancer. Methods: A computer-based retrieval of PubMed, EMBASE, Web of Science, CNKI and Wanfang Database was performed for correlative literature to aggregate the survival results from their establishment to September 2013. Relevant data were extracted from studies investigating the relationship between miR-200 family expression and survival in ovarian cancer patients. The data were analyzed with meta analysis using Stata vl 1.0 soRware. Results: Seven studies were identified, involving 577 cases with ovarian cancer. Meta-analysis results showed that, the combined hazard ratio (HR) for miR-200 family in ovarian cancer was 1.347 (95%CI: 1.052, 1.725). Subgroup ofmiR-200a, miR-200c and miR-141 subjects for survival were 1.091 (95%CI:0.718, 1.659), 1.285 (95%CI:0.765, 2.161 ), and 1.122 (95% CI: 1.043, 1.208), respectively. The risk ofmiR-200 family, miR-141 for prognosis in ovarian cancer patients was significant (P = 0.018, P = 0.002)). Conclusions: miR-200 family may act as a prognostic biomarker.
出处 《现代生物医学进展》 CAS 2015年第2期343-346,共4页 Progress in Modern Biomedicine
基金 广东省人口和计划生育委员会科研项目(20110272)
关键词 miR-200家族 卵巢癌 预后 肿瘤标记 META分析 miR-200 family Ovarian cancer Prognosis Tumor markers Meta analysis
  • 相关文献

参考文献25

  • 1Chao A, Lin CY, Lee YS, et al. Regulation of ovarian cancer progression by microRNA-187 through targeting Disabled homolog-2 [J]. Oncogene, 2012, 31(6): 764-775.
  • 2Calin GA, Sevignani C, Dumitru CD, et al. Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers[J]. Proc Natl Acad Sci U S A, 2004, 101(9): 2999-3004.
  • 3Hu X, Macdonald DM, Huettner PC, et al. A miR-200 microRNA cluster as prognostic marker in advanced ovarian cancer [J]. Gynecol Oncol, 2009, 114(3): 457-464.
  • 4Leskela S, Leandro-Garcia LJ, Mendiola M, et al. The miR-200 familycontrols beta-tubulin Ill expression and is associated with paclitaxel-based treatment response and progression-flee survival in ovarian cancer patients[J]. Endocr Relat Cancer, 2011, 18(1): 85-95.
  • 5Li S D, Zhang JR, Wang YQ, et al. The role of microRNAs in ovarian cancer initiation and progression [J]. J Cell Mol Med, 2010, 14(9): 2240-2249.
  • 6Mateescu B, Batista L, Cardon M, et al. miR-141 and miR-200a act on ovarian tumorigenesis by controlling oxidative stress response[J]. Nat Med, 2011, 17(12): 1627-1635.
  • 7Torres A, Torres K, Maciejewski R, et al. MicroRNAs and their role in gynecological tumors[J]. Med Res Rev, 2011, 31(6): 895-923.
  • 8Stroup DF, Berlin JA, Morton SC, et al. Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group [J]. JAMA, 2000, 283(15): 2008-2012.
  • 9Knobloch K, Yoon U, Vogt PM. Preferred reporting items for systematic reviews and meta-analyses (PRISMA) statement and publication bias[J]. J Craniomaxillofac Surg, 2011, 39(2): 91-92.
  • 10Zhang L, Riethdorf S, Wu G, et al. Meta-analysis of the prognostic value of circulating tumor cells in breast cancer [J]. Clin Cancer Res, 2012, 18(20): 5701-5710.

二级参考文献43

  • 1J emal A, Siegel R, Ward E, Hao Y, Xu J, Thun M J. Cancer statisties,2009[J]. CA Cancer J C1in,2009,59:225 -249.
  • 2Gregory P A,Bert A G,Paterson E L,Barry S C,Tsykin A, Farshid G, et al. The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1 [J]. Nat Cell Biol,2008,10:593 -601.
  • 3Zhang L, Huang J, Yang N, Greshock J, Megraw M S, Giannakakis A,et al. mieroRNAs exhibit high frequency genomic alterations in human cancer[J]. Proc Natl Acad Sci USA, 2006,103:9136-9141.
  • 4Nam E J,Yoon H,Kim S W,Kim H,Kim Y T,Kim J H,et al. MieroRNA expression profiles in serous ovarian carcinoma[J]. Clin Cancer Res, 2008, 14 :2690-2695.
  • 5Wyman S K,Parkin R K,Mitchell P S,Fritz B R,O'Briant K, Godwin A K, et al. Repertoire of microRNAs in epithelial ovarian cancer as determined by next generation sequencing of small RNA cDNA libraries[J]. PLoS One,2009,4:e5311.
  • 6Yang H,Kong W,He L,Zhao J J,O'Donnell J D,Wang J,et al. MicroRNA expression profiling in human ovarian cancer: miR-214 induces cell survival and cisplatin resistance by largeling PTEN [J].Cancer Res, 2008,68 : 425-433.
  • 7Li S D,Zhang J R,Wang Y Q,Wan X P. The role of microR-NAs in ovarian cancer initiation and progression[J]. J Cell Mol Med,2010,14:2240 -2249.
  • 8Bendoraite A,Knouf E C,Garg K S,Parkin R K,Kroh E M,O' Briant K C, et al. Regulation of miR-200 family microRNAs and ZEB transcription factors in ovarian cancer: evidence supporting a mesothelial to epithelial transition[J].Gynecol Oncol, 2010,116:117 -1125.
  • 9Olson P,Lu J,Zhang H,Shai A,Chun M G,Wang Y,et al. MicroRNA dynamics in the stages of tumorigenesis correlate with hallmark capabilities of caneer[J]. Genes Dev, 2009,23 : 2152- 2165.
  • 10Gibbons D L,Lin W,Creighton C J,Rizvi Z H,Gregory 17 A, Goodall G J, et al. Contextual extracellular cues promote tumor cell EMT and metastasis by regulating miR 200 family expression[J]. Genes Dev,2009,23:2140- 2151.

共引文献14

同被引文献23

引证文献3

二级引证文献4

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