期刊文献+

FHIT蛋白表达与外阴癌发生发展的关系 被引量:2

Relationship Between the Expression of Fragile Histidine (FHIT) and the Development of Vulvar Carcinoma
暂未订购
导出
摘要 目的探讨FHIT蛋白在外阴癌发生发展过程中的作用。方法用免疫组化SP法对20例正常外阴、22例外阴上皮内瘤样病变(VINs)及60例外阴癌组织分别进行FHIT蛋白表达的检测。结果正常外阴组织、低级别VINs、高级别VINs、外阴癌FHIT蛋白阳性表达率分别为100%(20/20),72.7%(8/11),45.5%(5/11),21.7%(13/60),差异有统计学意义(P<0.05)。在高、中、低分化的浸润性外阴癌中,FHIT蛋白的阳性表达率分别为60.0%(9/15),20.0%(3/15),3.3%(1/30),差异有统计学意义(P<0.05);有淋巴结转移者FHIT蛋白阳性表达率为10.0%(2/20),明显低于无淋巴结转移者的27.5%(11/40)。结论FHIT蛋白的异常表达在外阴癌的发展中起着重要作用,而且可为外阴癌的预后提供重要的信息。 Objective To explore the relationship betweenthe reduction of FHIT expression of fragile histidine (FHIT) and the development of vulvar carcinoma. Methods The expression of the FHIT product was detected by immunochemistry in the tissue samples of 20 normal vulvas, 22 vulvar intraepithelial neoplasias (VINs), and 60 primary vulvar carcinomas. Results The expressive rates of FHIT protein in the squamous epithelium of normal vulvas, VIN Ⅰ -Ⅱ , VIN Ⅲ, and noninvasive and invasive vulvar carcinoma were 100% (20/ 20), 72. 70% (8/11), 45. 5% (5/11), and 21.7% (13/60) respectively (P 〈 0. 05). The expressive rates of FHIT protein in the well differentiated, intermediately differentiated and poorly differentiated invasive vulav carcinoma were 60. 0%(9/15), 20. 0%(3/15), and 3. 3%(1/30) respectively (P〈0. 05). The expressive rate of the impaired FHIT protein in the invasive vulva carcinoma with lymphnode metastasis (10%) was lower than that without lymphnode metastasis (27.5%). Conclusion Abnormal FHIT expression may play an important role in the progression of vulvar carcinoma. The expression of FHIT may provide important information for the prognosis of vulva carcinoma.
出处 《四川大学学报(医学版)》 CAS CSCD 北大核心 2006年第2期218-220,共3页 Journal of Sichuan University(Medical Sciences)
基金 四川省科技厅应用基础资金(04JY029-077-2)资助
关键词 外阴癌 FHIT蛋白 外阴上皮内瘤样病变 Vulvar carcinoma FHIT-protein Vulvar intraepithelial neoplasias
  • 相关文献

参考文献2

二级参考文献54

  • 1Ogasawara S, Maesawa C, Tamura G, et al. Frequent microsatellite alterations on chromosome 3p in esophageal squamous cell carcinoma [J]. Cancer Res, 1995, 55 (4): 891- 894.
  • 2Hu N, Roth MJ, Polymeropolous M, et al. Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous cell carcinoma in a high risk Chinese population [J]. Genes Chromosomes Cancer, 2000, 27(3): 217- 228.
  • 3Ohta M, Inoue H, cotticelli MG, et al. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma associated t (3∶ 8) breakpoint, is abnormal in digestive tract cancers [J]. Cell, 1996, 84(4): 587- 597.
  • 4Virgilio L, Shuster M, Gollin SM, et al. FHIT gene alterations in head and neck squamous cell carcinomas [J]. Proc Natl Acad Sci USA, 1996, 93(18): 9770- 9775.
  • 5Sozzi G, Veronese ML, Negrini M, et al. The FHIT gene 3p14.2 in lung cancer [J]. Cell, 1996, 85(1): 17- 26.
  • 6Druck T, Hadaczek P, Fu TB, et al. Structure and expression if the human FHIT gene in normal and tumor cells [J]. Cancer Res, 1997, 57(3): 504- 512.
  • 7Hayashi S, Tanimoto K, Hajiro nakanishi K, et al. Abnormal FHIT transcripts in human breast carcinomas: a clinicopathological and epidemiological analysis of 61 Japanese cases [J]. Cancer Res, 1997, 57(10): 1981- 1985.
  • 8Luan X, Shi G, Zohouri M, et al. The FHIT gene is alternatively spliced in normal kidney and renal cell carcinoma [J]. Oncogene, 1997, 15(1): 79- 86.
  • 9Menin C, Sanacatterina M, Zambon A, et al. Anomalous transcripts and allelic deletions of the FHIT gene in human esophageal cancer [J]. Cancer Genet Cytogenet, 2000, 119(1): 56- 61.
  • 10Zou TT, Lei J, Shi YQ, et al. FHIT gene alterations in esophageal cancer and ulcerative colitis (UC) [J]. Oncogene, 1997, 15(1): 101- 105.

共引文献37

同被引文献14

  • 1张文淼,帅茨霞,郑飞云,黄引平,王群姬,朱华,何秋香.脆性组氨酸三联体基因在宫颈癌前病变和宫颈癌中的表达及其与p53和HPV16/18的关系[J].中华肿瘤杂志,2006,28(6):452-455. 被引量:26
  • 2李作生,李保庆.p21和p27基因多态性与肿瘤的相关性[J].国际遗传学杂志,2006,29(4):317-320. 被引量:25
  • 3[美]肯尼思A博哈特,[加]迈克尔A诺布尔.性传播疾病:流行病学、病理学、诊断和治疗[M].连石,等译.北京:科学技术文献出版社,2000:262-266.
  • 4Ohta M, Inoue H,Cotticelli MG, et al. The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma2associated t(3; 8) breakpoint is abnormal in digestive tract cancers[J]. Cell,1996,84(4): 587-597.
  • 5Boldog FL, Gemmilli RM, Wilke CM, et al. Position cloning of the hereditary renal carcinoma 3; 8 chromosome translocation breakpoint[J]. Proceedings of the National Academy of Sciences, 1993, 90(3): 8 509- 8 513.
  • 6Connolly DC,Greenspan JG,Wu R,et al. Loss of FHIT expression in invasive cervical carcinomas and intraepitheliallesions associated with invasive disease[J]. Clin Cancer Res,2000,6(9):3 505-3 510.
  • 7Uematsu K,Yoshimura A,Gemma A,et al. Aberrations in the fragile histidme triad(FHIT)gene in idiopathic pulmonary fibrosis[J]. Cancer Res,2001,61(23) :8 527- 8 533.
  • 8Wakasugi E, Kobayashi T, Tamaki Y, et al. p21 (waf1 / cip1) and p53 protein expression in breast cancer[J]. Am J Clin Pathol,1997,107(6) :684-691.
  • 9Sard L, Accornero P, Torniell S, et al. The tumorsuppressor gene FHIT is involved in the regulation of apoptosis and in cell cycle control[J]. Proceedings of the National Academy of Sciences, 1999,96 ( 15 ) : 8 489- 8 492.
  • 10谢宇,蒋先镇,江勃年,唐自元,谭春祈.FHIT、p21^(waf1/cip1)基因在膀胱移行细胞癌中的表达与意义[J].现代肿瘤医学,2007,15(9):1295-1297. 被引量:3

引证文献2

二级引证文献7

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