期刊文献+

鼻咽癌组织中miR-21的表达变化及意义 被引量:1

Expression and clinical significance of miR-21 in nasopharyngeal carcinoma
下载PDF
导出
摘要 目的观察鼻咽癌组织中miR-21的表达变化,并探讨其临床意义。方法收集54例鼻咽癌患者活检组织标本(观察组),35例正常及慢性鼻咽炎黏膜组织标本(对照组),采用实时荧光定量PCR(qRT-PCR)检测两组miR-21的表达,分析miR-21表达水平与鼻咽癌临床病理参数及与患者预后关系。结果观察组中miR-21平均表达量为(16.76±1.73)×10-3,对照组为(2.39±0.62)×10-3,两组比较,P<0.01。临床Ⅲ/Ⅳ期鼻咽癌miR-21表达水平明显高于临床Ⅰ/Ⅱ期鼻咽癌组织(P<0.05);有淋巴结转移的鼻咽癌组织明显高于无转移的鼻咽癌(P<0.01);Kaplan-Meier生存分析发现,miR-21表达越高患者生存率越低(P<0.05)。结论鼻咽癌组织中miR-21的表达明显升高,与鼻咽癌的发生、临床进展及预后密切相关,可能是鼻咽癌新的诊断预后分子标志物及潜在的治疗靶点。 Objective To investigate the expression and clinical significance of the miR-21 in tissue of nasopharyngeal carcinoma(NPC).Methods Biopsies of 54 cases of NPC(observed group) and 35 control tissues of normal and inflammatory nasopharyngeal cases(control group)were collected,and qRT-PCR was used to detect the miR-21 expression in those specimens.The correlation between the miR-21 expression and clinicopathologic parameter of NPC,prognosis were analyzed.Results The average expression level of miR-21 in observed group and control group was(16.76±1.73)×10-3 and(2.39±0.62)×10-3,which showed significant difference(P0.01).Moreover,the expression of miR-21 was higher in NPC stage Ⅲ/Ⅳ than that in stageⅠ/Ⅱ(P0.05);and tissue with lymph node metastasis was higher than that without lymph node metastasis(P0.01).By using Kaplan-Meier survival curves,NPC patients with relatively high expression of miR-21 showed higher mortality compared with low expression of miR-21.Conclusions The expression of miR-21 increases in tissue of NPC,which is associated with the carcinogenesis,progression,and prognosis of nasopharyngeal carcinoma and it can be used as a new biomarker of diagnosis and prognosis and a potential target of therapy and in NPC.
出处 《山东医药》 CAS 2012年第47期10-12,共3页 Shandong Medical Journal
基金 国家自然科学基金资助项目(81101526)
关键词 微小RNA-21 鼻咽肿瘤 鼻咽癌 miR-21 nasopharyngeal tumor nasopharyngeal carcinoma
  • 相关文献

参考文献16

  • 1He L,Hannon GJ. MicroRNAs:small RNAs with a big role in gene regulation[J].Nature Reviews Genetics,2004,(07):522-531.
  • 2Srivastava SK,Bhardwaj A,Singh S. MicroRNA-150 directly targets MUC4 and suppresses growth and malignant behavior of pancreatic cancer cells[J].Carcinogenesis,2011,(12):1832-1839.
  • 3Saini S,Yamamura S,Majid S. MicroRNA-708 induces apoptosis and suppresses tumorigenicity in renal cancer cells[J].Cancer Research,2011,(19):6208-6219.
  • 4Segura MF,Hanniford D,Menendez S. Aberrant miR-182 expression promotes melanoma metastasis by repressing FOXO3 and microphthalmia-associated transcription factor[J].Proceedings of the National Academy of Sciences(USA),2009,(06):1814-1819.doi:10.1073/pnas.0808263106.
  • 5Meng F,Henson R,Wehbe-Janek H. MicroRNA-21 regulates expression of the PTEN tumor suppressor gene in human hepatocellular cancer[J].Gastroenterology,2007,(02):647-658.
  • 6Chin LJ,Rather E,Leng S. A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk[J].Cancer Research,2008,(20):8535-8540.
  • 7Sengupta S,den Boon JA,Chen IH. MicroRNA 29c is down-regulated in nasopharyngeal carcinomas,up-regulating mRNAs encoding extracellular matrix proteins[J].Proceedings of the National Academy of Sciences(USA),2008,(15):5874-5878.
  • 8Zhu Q,Wang Z,Hu Y. miR-21 promotes migration and invasion by the miR-21-PDCD4-AP-1 feedback loop in human hepatocellular carcinoma[J].Oncology Reports,2012,(05):1660-1668.
  • 9Zhang BG,Li JF,Yu BQ. microRNA-21 promotes tumor proliferation and invasion in gastric cancer by targeting PTEN[J].Oncology Reports,2012,(04):1019-1026.
  • 10Vicinus B,Rubie C,Faust SK. miR-21 functionally interacts with the 3 'UTR of chemokine CCL20 and down-regulates CCL20 expression in miR-21 transfected colorectal cancer cells[J].Cancer Letters,2012,(01):105-112.

同被引文献14

  • 1HE L, HANNON G J. MicroRNAs: small RNAs with a big role in gene regulation [ J 1 .Nat Rev Genet, 2004, 5(7): 522-531.
  • 2CHEN P S, SU J L, HUNG M C. Dysregulation of MicroRNAs in cancer [ J ] J Biomed Sci, 2012, 19(1): 90.
  • 3MANIKANDAN J, AARTHI J J, KUMAR S D, et al. Oncomirs: the potential role of non-coding microRNAs in understanding cancer [ J ] . Bioinformation, 2008, 2(8): 330-334.
  • 4CHIN L J, RATNER E, LENG S, et al. A SNP in a let-7 mieroRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk [ J ] . Cancer Res, 2008, 68(20): 8535-8540.
  • 5SENGUPTA S, DEN BOON J A, CHEN I H, et al. MicroRNA 29c is down-regulated in nasopharyngeal carcinomas, up- regulating mRNAs encoding extraeellular matrix proteins [ J] . Proe Natl Acad Sci U S A, 2008, 105(15): 5874-5878.
  • 6ZHU Q, WANG Z, HU Y, et al. miR-21 promotes migration and invasion by the miR-21-PDCD4-AP-1 feedback loop in human hepatoeellular carcinoma [ J ] . Oncol Rep, 2012, 27(5): 1660-1668.
  • 7ZHANG B G, LI J F, YU B Q, et al. microRNA-21 promotes tumor proliferation and invasion in gastric cancer by targeting PTEN [ J ]. Oncol Rep, 2012, 27(4): 1019-1026.
  • 8DARIDO C, GEORGY S R, WILANOWSKI T, et al. Targeting of the tumor suppressor GRHL3 by a miR-21- dependent proto-oncogenic network results in PTEN loss and tumorigenesis [ J ] . Cancer Cell, 2011, 20(5): 635-648.
  • 9VICINUS B, RUBIE C, FAUST S K, et al. miR-21 functionally interacts with the 3' UTR of chemokine CCL20 and down- regulates CCL20 expression in miR-21 transfected colorectal cancer cells [ J ] . Cancer Lett, 2012, 316(1): 105-112.
  • 10MEDINA P P, NOLDE M, SLACK F J. OncomiR addiction in an in vivo model of microRNA-21-induced pre-B-cell lymphoma [ J ] . Nature, 2010, 467(7311): 86-90.

引证文献1

二级引证文献3

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