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微小RNA Let-7a在子宫颈鳞状细胞癌发生发展过程中的作用及相关性研究
作者:朱峻峰1  陈路2  王清2  毛愿舒1  唐立华2 
单位:1. 宜昌市妇幼保健院 妇产科, 湖北 宜昌 443003;
2. 宜昌市中心医院 病理科, 湖北 宜昌 443003
关键词:miRNA let-7a 人乳头状瘤病毒 鳞状上皮内病变 子宫颈鳞状细胞癌 
分类号:R737.33
出版年·卷·期(页码):2018·37·第四期(616-619)
摘要:

目的:研究微小RNA Let-7a(miRNA Let-7a)在人乳头状瘤病毒(HPV)阴性组、HPV阳性组宫颈组织中的差异性表达,初步探讨其在HPV诱导子宫颈鳞状细胞癌的发生、发展过程中的作用。方法:通过HPV分型检测将宫颈脱落细胞及子宫颈活检样本分为HPV阴性组、低危HPV感染组、高危HPV感染组,结合病理学活检将高危HPV感染组分为慢性子宫颈炎组、低级别鳞状上皮内病变(LSIL)组、高级别鳞状上皮内病变(HSIL)组及子宫颈鳞状细胞癌组,用RT-PCR法对各组间miRNA Let-7a表达水平进行定量及差异性分析。结果:宫颈脱落细胞中miRNA Let-7a表达水平在HPV感染组显著低于HPV阴性组(P<0.01),而高危与低危间差异无统计学意义;组织活检样本中miRNA Let-7a表达水平在鳞状上皮内病变及鳞状细胞癌中显著下降(P<0.01),而鳞状上皮内病变与鳞状细胞癌组间差异无统计学意义。结论:HPV感染能显著降低子宫颈上皮细胞中miRNA Let-7a表达水平;且在HPV感染的组织学样本中,鳞状上皮内病变及鳞状细胞癌组中miRNA Let-7a水平显著低于炎性对照组。提示miRNA Let-7a水平下降是HPV介导的子宫颈鳞状细胞癌的发病机制之一。

参考文献:

[1] MUNOZ N,BOSCH F X,DE SANJOSE S,et al.Epidemiologic classification of human papillomavirus types associated with cervical cancer[J].N Engl J Med,2003,348(6):518-527.
[2] MATSUKURA T,SUGASE M.Pitfalls in the epidemiologic classification of human papillomavirus types associated with cervical cancer using polymerase chain reaction:driver and passenger[J].Int J Gynecol Cancer,2008,18(5):1042-1050.
[3] THOMISON J R,THOMAS L K,SHROYER K R.Human papillomavirus:molecular and cytologic/histologic aspects related to cervical intraepithelial neoplasia and carcinoma[J].Hum Pathol,2008,39(2):154-166.
[4] XU B,LI J,LIU X,ET A L.TXNDC5 is a cervical tumor susceptibility gene that stimulates cell migration,vasculogenic mimicry and angiogenesis by down-regulating SERPINF1 and TRAF1 expression[J].Oncotarget,2017,8(53):91009-91024.
[5] CHENG Y,GENG L,ZHAO L,et al.Human papillomavirus E6-regulated microRNA-20b promotes invasion in cervical cancer by targeting tissue inhibitor of metalloproteinase 2[J].Mol Med Rep,2017,16(4):5464-5470.
[6] 王美藏,高建宏,杨雅琴,等.子宫颈HPV感染与MCM2蛋白表达及阴道环境因素的相关性分析[J].现代医学,2017,45(1):23-27.
[7] MONDOL V,PASQUINELLI A E.Let's make it happen:the role of let-7 microRNA indevelopment[J]. Curr Top Dev Biol,2012,99:1-30.
[8] HO C S,YAP S H,PHUAH N H,et al.MicroRNAs associated with tumour migration,invasion and angiogenic properties in A549 and SK-Lul human lung adenocar cinoma cells[J].Lung Cancer,2014,83(2):154-162.
[9] THIRION M,OCHIYA T.Roles of microRNAs in the hepatitis B virus infection and related diseases[J].Viruses,2013,5(11):2690-2703.
[10] WU W,SUN M,ZOU G M,et al.MicroRNA and cancer:current status and prospective[J].Int J Cancer,2007,120(5):953-960.
[11] ESQUELA-KERSCHER A,SLACK F J.Oncomirs-microRNAs with a role in cancer[J].Nat Rev Cancer,2006,6(4):259-269.
[12] IORIO M V,CROCE C M.MicroRNAs in cancer:small molecules with a huge impact[J].J Clin Oncol,2009,27(34):5848-5856.
[13] CARLETON M,CLEARY M A,LINSLEY P S.MicroRNAs and cell cycle regulation[J].Cell Cycle,2007,6(17):2127-2132.
[14] REINHART B J,SLACK F J,BASSON M,et al.The 21-nucleotide let-RNA regulates developmental timing in Caenorhabditis elegans[J].Nature,2000,403(6772):901-906.
[15] TAKAMIZAWA J,KONISHI H,YANAGISAWA K,et al.Reduced expression of the let-7 microRNAs in human lung cancers in association with shortened postoperative survival[J].Cancer Res,2004,64(11):3753.
[16] NICOLOSO M,SPIZZO R,SHIMIZU M,et al.MicroRNAs-the micro steering wheel of tumour metastases[J].Nat Rev Cancer,2009,9(4):293-302.
[17] SHEN Y,LI Y,YE F,et al.Identification of miR-23a as a novel microRNA normalizer for relative quantification in human uterine cervical tissues[J].Exp Mol Med,2011,43(6):358-366.

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