期刊文献+

miR-21在上皮性卵巢癌组织中的表达及临床意义 被引量:14

Expression of microRNA-21 in ovarian epithelial carcinoma and its clinical significance
下载PDF
导出
摘要 目的探讨微小RNA-21(miR-21)在上皮性卵巢癌组织中的表达及其与临床病理特征间的关系。方法采用茎环实时荧光逆转录聚合酶链反应(real-timeRT-PCR)检测48例上皮性卵巢癌组织、24例良性上皮性卵巢肿瘤及15例正常卵巢组织标本中miR-21表达。结果茎环real-timeRT-PCR检测miR-21表达的敏感性和特异性良好;miR-21在卵巢癌组织中的相对表达量(4.849±1.813)显著高于良性卵巢肿瘤(1.133±0.291)及正常卵巢组织(P<0.01),后两组间miR-21表达无明显差异。miR-21表达随卵巢癌的临床分期和组织分级的进展呈上升趋势,而且在有淋巴结转移组明显高于无淋巴结转移组(P均<0.01)。结论miR-21在上皮性卵巢癌组织中的表达升高,提示其可能在卵巢癌的发生发展中发挥致癌基因的作用,并且与卵巢癌的演进及不良预后密切相关。 Objective To investigate the expression of microRNA-21 (miR-21) in ovarian epithelial carcinoma and its association with the clinicopathological features. Methods The expression of miR-21 was detected by Stem-loop real-time RT-PCR in 48 cases of ovarian epithelial carcinomas, 24 cases of benign ovarian epithelial tumors and 15 cases of normal ovarian tissues. Results The relative expression level of miR-21 (2- △△CT) was 4.849 ±1.813 in the ovarian epithelial carcinomas, significantly higher than that in the benign ovarian tumors and normal ovarian tissues (P0.01), but comparable between the latter two groups. The expression of miR-21 was not correlated to the histological type, but increased significantly with the progression of the clinical stages and histological grading (P0.01), showing a close correlation to lymphatic metastasis. Conclusion MiR-21 might play a role as an oncogene in the tumorigenesis and development of ovarian epithelial carcinoma, and is possibly correlated to the progression and prognosis of ovarian epithelial carcinoma.
出处 《南方医科大学学报》 CAS CSCD 北大核心 2010年第3期608-610,613,共4页 Journal of Southern Medical University
关键词 上皮性卵巢癌 微小RNA-21 real-time RT-PCR ovarian epithelial carcinoma microRNA-21 real-time reverse transcription-polymerase chain reaction
  • 相关文献

参考文献10

  • 1lorio MY, Fcrracin M, Liu CG, et al. MicroRNA gene expression deregulation in human breast cancer[J]. Cancer Res, 2005, 65(16): 7065-70.
  • 2Chan JA, Kriehevsky AM, Kosik KS. MicroRNA-21 is an antiapoptotie factor in human glioblastoma cells[J]. Cancer Bes, 2005, 65 (14): 6029-33.
  • 3Hede IC Studies define role ofmicroRNA in cancer[J]. J Natl Cancer Inst, 2005, 97(15): 1114 -5.
  • 4Gregory RI, Shiekhattar R. MicroRNA biogenesis and cancer [J]. Cancer Res, 2005, 65(9): 3509-12.
  • 5Lui WO, Pourmand N, Patterson BK, et al. Patterns of known and novel small RNAs in human cervical cancer[J]. Cancer Res, 2007, 67(13): 6031-43.
  • 6Narn E J, Yoon H, Kim SW, et al. MicroRNA expression profiles in serous ovarian carcinoma[J].Clin Cancer Res, 2008, 14(9): 2690-5.
  • 7马卓娅,汤华,李欣,刘民,吴海东,王晶.MicroRNA在六种不同器官肿瘤细胞系中的差异表达[J].中国肿瘤,2007,16(9):714-717. 被引量:9
  • 8Iorio MV, Visone R, Di Leva G, et al. MicroRNA signatures in human ovarian cancer[J]. Cancer Res, 2007, 67(18): 8699-707.
  • 9Meng F, Henson R, Wehbe-Janek H, et al. MicroRNA-2 1 regulates expression of the PTEN tumor suppressor gene in human hepatoeellular cancer[J]. Gastroenterology, 2007, 133(2): 647-58.
  • 10Li AJ, Karlan BY. Genetic factors in ovarian carcinoma [J]. Curr Oncon Rep, 2001, 3(1): 27-32.

二级参考文献12

  • 1马卓娅,汤华.microRNA与肿瘤[J].生命的化学,2006,26(1):2-5. 被引量:10
  • 2Bartel DP.microRNAs:genomics,biogenesis,mechanism,and function[J].Cell,2004,116(2):281-297.
  • 3Bentwich I,Avniel A,Karov Y,et al.Identification of hundreds of conserved and nonconserved human microRNAs[J].Nat Genet,2005,37(7):766-770.
  • 4Berezikov E,Guryev V,vande BJ,et al.Phylogenetic shadowing and computational identificafion of human micmRNA genes[J].Cell,2005,120(1):21-22.
  • 5Lewis BP,Burge CB,Bartel DP.Conserved seed pairing,often flanked by adenosines,indicates that thousands of human genes are microRNA targets[J].Cell,2005,120(1):15-20.
  • 6David Brown,Jaclyn Shingara,Kerri Keiger,et al.Cancer Related miRNAs Uncovered by the mirVana^TM miRNA Microarray Platform[R].Ambion Technotes,2005.12(1):8-11.www.amkion.com/techilb/tn/121/4.html.
  • 7Iorio MV,Ferracin M,Liu CG,et al.MicroRNA gene expression deregulation in human breast cancer[J].Cancer Res,2005,65(16):7065-7070.
  • 8Calin 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.
  • 9Ota A,Tagawa H,Kaman S,et al.Identification and characterization of a novel gene,C13 or f25,as a target for 13q31-q32 amplification in malignant lymphoma[J].Cancer Res,2004,64(9):3087-3095.
  • 10O'Donnell KA,Wentzel EA,Zeller KI,et al.c-Mye-regulated microRNAs modulate E2F1 expression[J].Nature,2005,435(7043):839-843.

共引文献8

同被引文献174

引证文献14

二级引证文献77

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