期刊文献+

FHIT、HPV16/18在宫颈鳞癌中的表达及意义 被引量:4

The expression and significance of the FHIT and HPV16/18 in cervical cancer
下载PDF
导出
摘要 目的探讨脆性组氨酸三联体(Fragile histidine triad)基因(FHIT)及HPV16/18与宫颈癌发病的关系。方法采用免疫组化法检测50例宫颈鳞癌组织、50例正常宫颈组织中的FHIT基因表达情况和HPV感染情况。结果FHIT在正常宫颈组织中的阳性表达率为72%(36/50),在宫颈鳞癌组织中的阳性表达率为32%(16/50),明显低于正常宫颈组织组P<0.001。HPV16/18在正常宫颈组织的阳性率为12%(6/50),在宫颈鳞癌组的阳性率为72%(36/50),两组间比较有统计学差异P<0.001。相关分析提示FHIT蛋白缺失与HPV16/18感染无相关关系。结论FHIT基因缺失及HPV16/18感染与宫颈癌的发生有关。HPV感染与FHIT蛋白缺失异常是导致宫颈鳞癌的两个独立原因。 Objective To evaluate the relationship between fragile histidine triad (FHIT) transcription abnormalities and HPV16/18 infection and human cervical tumorigenesis. Methods The immunohistochemisloy was used to detect the expression of FHIT and HPV16/18 in normal tissue and in cancer tissue. Results In normal cervices and in cervical cancers, the positive rates of FHIT protein expression amounted to 72% (36/50) and 32% (16/50) respectively, and there were statistics significant differences (P〈0. 001). The positive rates of HPV16/18 were 36% (18/50) and 72% (36/50) respectively, and there were also statistics significant differences between the normal cervices group and cervical cancers group (P〈0. 05). The analysis show that there were no correlation between the expression of HPV16/18 and FHIT protein (r=-0. 089). Conclusion The default of FHIT and infection of HPV16/18 are correlated with cervical cancer. HPV infection and FHIT protein default are the two independent causes of cervical cancer.
出处 《贵州医药》 CAS 2009年第4期305-307,共3页 Guizhou Medical Journal
关键词 FHIT基因 HPV16/18感染 宫颈鳞癌 Fragile histidine triad (FHIT) HPV16/18 infection Cervical cancer
  • 相关文献

参考文献13

  • 1Ohta M, Inoue H, Cotticelli MG, et al. The FHIT gene, spanning the chromosome 3p14. 2 fragile site and renal carcinomaassociated t(3 ;8) breakpoint, is abnormal in digestive tract cancers[J]. Cell, 1996, 84 (4) : 587-597.
  • 2Chaudhuri AR, Khan IA, Prasad V, et al. The tumor suppressor protein FHIT. A novel interaction with tu- bulin[J]. J Biol Chem, 1999, 274:173-180.
  • 3Huang LW, Chao SL, Chen TJ. Reduced FHIT expression in cervical carcinoma: correlation with tumor progression and poor prognosis[J]. Gyneeol Oneol, 2003, 90: 331-337.
  • 4Helland A, Kraggerud SM, Kristensen GB, et al. Primary cervical carcinomas show 2 common regions of deletion at 3P, 1 within the FHIT gene: evaluation of allelie imbalance at FHIT, RB1 and TP53 in relation to survival[J]. Int J Cancer, 2000, 88(2): 217-222.
  • 5Munoz N, Bosch F X, Sanjose S, et al. Epidemiologic classification of human papillomavirus types associated with cervical cancer[J]. N Engl J Med, 2003, 348 (6) : 518-527.
  • 6Einstein M H, Goldberg G L. Human papillomavirus and cervical neoplasia[J]. Cancer Invest, 2002, 20(7- 8) : 1080-1085.
  • 7Bosch F X, Munoz N. The viral etiology of cervical cancer[J]. Virus Res, 2002, 89(2): 183-190.
  • 8Bernhard Kleter, LeenJan Van Doom, Lianne Schrauwen et al. Development and clinical evaluation of a highly sensitive PCR-reverse hybridization line probe assay for detection and identification of anogenital human papillomavirus[J]. Journal of Clinical Microbiology, 1999,37(8) : 2508-2517.
  • 9范翠芳,欧阳耀灵,胡萍.端粒酶活性、HPV与宫颈癌的研究进展[J].长江大学学报(自然科学版),2005,2(3):100-101. 被引量:5
  • 10Koromilas AE, Li S, Matlashewski G. Control of interferon signaling in human papillomavirus infection [J]. Cytokine Growth Factor Rev, 2001, 12 (2-3). 157-170.

二级参考文献8

  • 1Pao C C,Tseng C J,Lin C Y et al.Differential expression of telomerase activity in human cervical carcer and cervical intraepithelial neoplasia lesions[].Journal of Clinical Oncology.1997
  • 2Takakura M,Kyo S,Kanaya T et al.Expression of human telomerase subunits and correlation with human telomerase activity in cervical carcer[].Cancer Research.1998
  • 3Nagai N,Oshita T,Murakani J et al.Semiquantitive analysis of telomerase activity in cervical cancer and precancerous lesions[].Oncology Reports.1999
  • 4Zhang A,Zheng C,Hou M et al.Ampliification of the telomerase reverse transcriptase ( hTERT) gene in cervical carcinoms[].Genes Chromosomes Cancer.2002
  • 5Veldman T,Liu X,Yuan H et al.Human papillomaviirusE6 and Myc proteins associate in vivo and bind to and cooperatively activte the telomerase reverse transcriptase promoter[].Proceedings of the National Academy of Sciences of the United States of America.2003
  • 6Boldrini L,Faviana P,Gisfredi S et al.Regulation oftelomerase its hTERT messenger in colorectal cancer[].Oncology Reports.2004
  • 7Won J,Yim J,Kim T K.Oppoosing regulatory roles of E2 Fin human telomerase reverse transcriptase (hTERT) gene expression in human tumor and nomal somatic ceels[].The FASEBJ Journal.2002
  • 8CuzickJ,TerryG,HoLetal,HollingwothT,AndersonM.HumanpapillomaviirusDNAinabnomalsmearsasapridectorofhigh gradecervicalintraepithelialneoplasia[].British Journal of Cancer.1994

共引文献4

同被引文献29

  • 1吕晓萍,李体远,戴勇,童秋生,熊峰,李放娟,季卉,许小庄.人乳头状瘤病毒快速导流杂交与传统杂交法比较基因分型及临床应用[J].中华医院感染学杂志,2005,15(6):618-621. 被引量:18
  • 2Chan P K, Mak K H, Cheung J L, et al. Genotype spectrum of cervical human papillomavirus infection among sexually transmitted disease clinic patients in Hong Kong[J].J Med Virol,2002,68(2):273-277.
  • 3Walboomers J M, Jacobs M V, Manos M M, et al. Human papillomavirus is a necessary cause of invasive cervical cancer worldwide[J]. Pathology, 1999,189(1) : 12-19.
  • 4Munoz N, Bosch F X, Sanjose S, et al. Epidemiologic classification of human papillomavirus types associated with cervicalcancer[J]. N EnglJ Med,2003,348(6):518-527.
  • 5Clifford G M, Smith J S, Plummer M, et al. Human papillomavirus types in invasive cervical cancer worldwide: a meta-analysis[J]. Br J Cancer, 2003,88 (1) : 63-73.
  • 6Chan P K, Chang A R, Cheung J L, et ah Determinants of cervical human papillomavirus infection: differences between high- and low-oncogenic risk types[J]. J Infect Dis, 2002,185 (1) :28-35.
  • 7Liaw K L, Hsing A W, Chen C J, et al. Human papillomavirus and cervical neoplasia: a case control study in Taiwan[J]. Int J Cancer,1995,62(5):565-571.
  • 8Walboomers JM,Jacobs MV,Manos MM et al.Human papil-lomavirus is a necessary cause of invasive cervical cancer worldwide[J].Pathology,1999,189(1):12.
  • 9Clifford GM,Smith JS,Plummer M et al.Human papilloma-virus types in invasive cancer worldwide:a meta-analysis[J].Br J Cancer,2003,88:63.
  • 10Biedermann K,Dandachi N,Trattner M et al.Comparison of real-time PCR signal-amplified in situ hybridization and conventional PCR for detection and quantification of human papillomavirus in archival cervical cancer tissue[J].J Clin Microbiol,2004,42:3758.

引证文献4

二级引证文献28

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