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miR-200a在外阴鳞癌组织中的表达及临床意义 被引量:1

Expression and clinical significance of miR-200a in vulvar squamous cell carcinoma
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摘要 目的:分析外阴鳞癌(vulvar squamous cell carcinoma,VSCC)组织中微小RNA-200a(miR-200a)的表达及其临床意义。方法:通过RT-PCR检测外阴鳞癌组织25例、外阴上皮内非瘤样病变组织30例(其中包括外阴增生性营养不良15例、外阴萎缩性营养不良15例)以及正常外阴组织10例中miR-200a的表达。结果:miR-200a在外阴鳞癌组织中的相对表达量为(1.162±0.421),低于外阴上皮内非瘤样病变组织(2.723±1.151)及正常外阴皮肤组织(4.341±1.507)(P<0.05),但在外阴上皮内非瘤样病变组织及正常外阴组织间表达量无明显差异。在不同临床分期、不同组织学分级的外阴鳞癌组织中miR-200a表达量有统计学差异(P<0.05)。结论:miR-200a在外阴鳞癌组织中的表达下调,提示其可能在外阴鳞癌的发生发展中起到抑癌基因的作用。 Objective: To analyze the expression and clinical significance of miR - 200a in vulvar squamous cell carcinoma ( VSCC ) . Methods : The expressions of miR - 200a in 25 cases with VSCC, 30 cases with nonneopiastie epithelial disorders of vulve ( in- cluding 15 cases with vulvar hyperplastic dystrophy and 15 cases with vulval atrophic malnutrition), and 10 cases with normal vulvar tissue were detected by RT - PCR. Results : The relative expression level of miR - 200a in cases with VSCC was ( 1. 162 ~ 0. 421 ), which was statistically significantly lower than those in cases with nonneoplastic epithelial disorders of vulvar (2. 723 ± 1. 151 ) and cases with normal vulvar tissue(4. 341 ± 1. 507 ) (P 〈 0. 05 ) , but there was no significant difference between cases with nonneoplastic epithelial disorders of vulvar and cases with normal vulvar tissue. There was statistically significant difference in miR - 200a expression level among cases with VSCC of different clinical stages and histological grades ( P 〈 0. 05 ) . Conclusion : Down - regulation of miR - 200a in cases with VSCC indicates that miR - 200a might play a role as an anti - oncogene in pathogenesis and development of VSCC.
出处 《中国妇幼保健》 CAS 北大核心 2013年第17期2697-2699,共3页 Maternal and Child Health Care of China
基金 辽宁省自然科学基金项目〔20092095〕
关键词 微小RNA-200a 外阴鳞癌 RT-PCR microRNA - 200a Vulvar squamous cell carcinoma RT - PCR
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  • 1Thornburg NJ,Hayward SL,Crowe JE Jr.Respiratory syncytial virus regulates human microRNAs by using mechanisms in-volving beta interferon and NF-κB[J].MBio,2012,3(6):220.
  • 2Bracken CP,Gregory PA,Kolesnikoff N et al.A double-negative feedback loop between ZEB1-SIP1 and the microR-NA-200 family regulates epithelial-mesenchymal transition[J].Cancer Res,2008,68(19):7846.
  • 3Li X,Abdel-Mageed AB,Mondal D et al.MicroRNA expres-sion profiles in differentiated thyroid cancer,a review[J].Int J Clin Exp Med,2012,6(1):74.
  • 4Tavazoie SF,Alarcon C,Oskarsson T et al.Endogenous human microRNAs that suppress breast cancer metastasis[J].Na-ture,2008,451(4):147.
  • 5Nam EJ,Yoon H,Kim SW et al.MicroRNA expression profiles in serous ovarian carcinoma[J].Clin Cancer Res,2008,14(9):2690.
  • 6Hu X,Macdonald DM,Huettner PC et al.A miR-200 mi-croRNA cluster as prognostic marker in advanced ovarian canc-er[J].Gynecol Oncol,2009,114(3):457.
  • 7Lee JW,Choi CH,Choi J et al.Altered MicroRNA expression in cervical carcinomas[J].Clin Cancer Res,2008,14(9):2535.
  • 8Lui 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.
  • 9Hu X,Schwarz JK,Lewis JS et al.A microRNA expression signature for cervical cancer prognosis[J].Cancer Res,2010,70(4):1441.
  • 10Jaime Snowdon,Xiao Zhang,Tim Childs et al.The micro RNA-200 family is upregulated in endometrial carcinoma[J].Cancer Res,2011,71(8):9041.

同被引文献10

  • 1Bracken CP,Gregory PA,Kolesnikoff N,et al.A double-negative feedback loop between ZEB1 -SIP1 and the microRNA-200 family regulates epithelial-mesenchymal transition[J].Cancer Res,2008,68(19):7846-7854.
  • 2Tulalamba W,Janvilisri T.Nasopharyngeal carcinoma signaling pathway:an update on molecular biomarkers [J].Int J Cell Biol,2012(2012):594-681.
  • 3Cascio S,D'Andrea A,Ferla Rt et al.miR-20b modulates VEGF expression by targeting HIF-1 alpha and STAT3 in MCF-7 breast cancer celis[J].J Cell Physiol,2010,224(1):242-249.
  • 4Xia H,Ng SS,Jiang S,et al.miR-200a-mediated downregulation of ZEB2 and CTNNB1 differentially inhibits nasopharyngeal carci- noma cell growth,migration and invasion [J].Biochem Biophys Res Commun,2010,391(1):535-541.
  • 5Cochrane DR,SpoeIstra NS,Howe EN,et al.MicroRNA-200c,mitigates invasiveness and restores sensitivity to microtubule-targe- ting chemotherapeutic agents [J].Mol Cancer Ther,2009,8(5):1055-1066.
  • 6Chen HC,Chen GH,Chen YH,et al.MicroRNA deregulation and pathway alterations in nasopharyngeal carcinoma [J].Br J Cancer,2009,100(6):1002-1011.
  • 7刘锋,王占祥.miR-200与肿瘤侵袭转移关系的研究进展[J].现代肿瘤医学,2013,21(6):1410-1413. 被引量:3
  • 8王小军,周良芬,张华.miR-200c在肝细胞癌组织中的表达及其临床意义[J].中国现代医生,2013,51(28):1-3. 被引量:4
  • 9刘鹏,谭盛葵,肖胜军,易世江,熊伟明,侯巧燕,欧阳磊,雷迅.鼻咽癌中E-cadherin和β-catenin的表达及意义[J].临床与实验病理学杂志,2013,29(11):1222-1225. 被引量:9
  • 10王勇,李宇男,于晓松.肺癌细胞及组织中miR-181a、miR-200a、miR-200c表达变化及意义[J].山东医药,2014,54(48):16-18. 被引量:7

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