期刊文献+

hTERC基因的FISH检测对良恶性腹水鉴别诊断的价值

The differential diagnostic value of hTERC oncogene in benign and malignant ascites by fluorescence in situ hybridization
下载PDF
导出
摘要 目的检测腹水脱落细胞端粒酶(hTERC)基因的状态,以探讨其在良恶性腹水鉴别诊断中的价值。方法采用荧光原位杂交(FISH)方法,检测26例恶性腹水和15例良性腹水(对照组)脱落细胞hTERC基因的状态。结果①hTERC基因在良性腹水和恶性腹水中的扩增阳性率分别为6.7%和88.5%,恶性组显著高于良性组(P<0.05)。②恶性腹水中,FISH检测阳性率88.5%明显高于细胞学检测阳性率46.2%(P<0.05);良性腹水中,FISH诊断特异性略低于细胞学检查结果(93.3%和100%),但无统计学意义(P>0.05)。③不同肿瘤引起的腹水hTERC基因扩增阳性率比较差异无统计学意义(P>0.05)。结论恶性腹水hTERC基因高度扩增,检测该基因对良恶性腹水有重要鉴别诊断价值,尤其对细胞学检查阴性的患者。 Objective To investigate the state of hTERC oncogene in ascitic exfoliative cells, and to evaluate the effect and clinical significance of hTERC in benign and malignant ascitcs. Methods The fluorescent in situ hybridization (FISH) was used to detect the state of hTERC oncogene in 26 patients with various malignant ascites and 15 with benign ascites. Results (1) Positive amplification rates of hTERC in benign and malignant ascites were 6.7% and 88.5 % , respectively. The amplification in benign ascites were lower than that in malignant ascites (P 〈 0.05 ). (2) In malignant ascites ,the positive rates by cytology (46.2%) were lower than those by FISH(88.5% ) (P 〈 0. 05 );In benign ascites, the specificity of diagnosis by FISH was slightly lower than that by cytology result (93.3% and 100% ), but there was no significant difference (P 〉 0. 05 ). In addition, the positive amplification rate of the hTERC gene were no significant difference between malignant ascites (P 〉 0. 05 ). Conclusions hTERC gene is high amplification in malignant ascites, and it may be useful in differential diagnosis of benign and malignant ascites, particularly in cases of negative cytology.
出处 《安徽医科大学学报》 CAS 北大核心 2009年第5期554-557,共4页 Acta Universitatis Medicinalis Anhui
基金 卫生部医药卫生科技发展中心项目(编号:WKJ2007-3-001)
关键词 原位杂交 荧光 端粒末端转移酶 腹水/诊断 in situ hybridization fluorescence telomere ascites/diagnosis
  • 相关文献

参考文献15

二级参考文献80

  • 1陈道桢,耿金花,薛文群,张丽珊.染色体不稳定性及其与妇科肿瘤形成关系的研究进展[J].东南大学学报(医学版),2004,23(5):355-357. 被引量:9
  • 2Heselmeyer-Haddad K, Janz V, Castle PE, et al. Detection of genomic amplification of the human telomerase gene (TERC) in cytologic specimens as a genetic test for the diagnosis of cervical dysplasia [ J ]. Am J of Pathol, 2003, 163 : 1406-1416 被引量:1
  • 3Umayahara K, Numa F, Suehiro Y, et al. Comparative genomic hybridization detects genetic alterations during early stages of cervical cancer progression [ J ]. Genes Chromosomes Cancer,2002,33:98-102 被引量:1
  • 4Kloth JN, Oosting J, van Wezel T, et al. Combined arraycomparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer [ J ]. BMC Genomics, 2007,8 : 53-66 被引量:1
  • 5Olaharskil AJ, Sotelo R, Solorza-Luna G, et al. Tetraploidy and chromosomal instability are early events during cervical carcinogenesis [ J ]. Carcinogenesis, 2006,27 : 337-343 被引量:1
  • 6Kersemaekers AM, van de Vijver M J, Kenter GG, et al. Genetic alterations during the progression of squamous cell carcinomas of the uterine cervix [ J ]. Genes Chromosomes Cancer, 1999,26 : 346 -354 被引量:1
  • 7Heselmeyer K, Schrock E, du Manoir S, et al. Gain of chromosome 3q defines the transition from severe dysplasia to invasive carcinoma of the uterine cervix [ J ]. Proc Natl Acad Sci, 1996,93:479-484 被引量:1
  • 8Heselmeyer-Haddad K, Sommerfeld K, White NM, et al. Genomic amplification of the human telomerase gene (TERC) in pap smears predicts the development of cervical cancer[ J]. Am J Pathol,2005,166 : 1229-1238 被引量:1
  • 9Andersson S, Wallin KL, Hellstrom AC, et al. Frequent gain of the human telomerase gene TERC at 3q26 in cervical adenocarcinomas [ J ]. Br J Cancer, 2006,95 : 331- 338 被引量:1
  • 10Hopman AH, Theelen W, Hommelberg PP, et al. Genomic integration of oncogenic HPV and gain of the human telomerase gene TERC at 3q26 are strongly associated events in the progression of uterine cervical dysplasia to invasive cancer[ J ]. J Pathol,2006 ,210 :412419 被引量:1

共引文献136

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