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宫颈癌放疗前后FHIT蛋白的表达及与放疗疗效的关系 被引量:3

The expression of FHIT protein in cervical carcinoma and the relationship between expression of FHIT and treatment effect of radiotherapy.
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摘要 目的:探讨宫颈癌脆性组氨酸三联体基因(FHIT)蛋白表达与患者临床病理指标、放疗疗效及无瘤生存时间的关系。方法:用免疫组化法检测50例ⅡB~ⅢB期宫颈癌放疗前、DT10Gy,DT30Gy放疗中和放疗后FHIT蛋白的表达。结果:(1)放疗前50例患者FHIT蛋白表达阳性率36%,与病理分级,淋巴结转移有关,与年龄、临床分期、肿瘤大小无关;(2)放疗DT10Gy,DT30Gy和放疗结束后50例患者FHIT蛋白表达阳性率分别为56%,68%和84%,比放疗前明显升高(P<0.05);(3)放疗前FHIT蛋白阳性表达和阴性表达患者的放疗疗效分别为88.8%和59.4%,差异有统计学意义(P<0.05);(4)FHIT阳性表达无瘤生存时间与FHIT阴性表达无瘤生存时间无显著差异。结论:FHIT基因在宫颈癌发生发展中起重要作用,放疗可引起FHIT表达增加,FHIT蛋白的表达有助于判断宫颈癌患者放疗的敏感性。 Objective:To investigate the relationship between FHIT expression and the clinical pathological feature, treatment effect of radiotherapy, and the time of no disease in cervi- cal carcinoma. Method: Expression of FHIT protein was detected by immunohistochemical in 50 cases of squamous cell cervical carcinoma. Results: The positive rates of FHIT expression before radiotherapy DT10Gy, DT30Gy and after radiotherapy were 36% ,56% ,68% and 84% ,respec- tively(P〈0.05). There were significant differences between FHIT expression and histological grades and lymph node metastasis (P〈0.05). FHIT expression was not correlated with age, clinical stage and diameter of the turnout(P〉0.05). There was a significant correlation between FHIT expression and treatment effect of radiotherapy(P〈0.05 ). FHIT expression was not corre- lated with the time of no disease. Conclusion:FHIT may be very important in development of cervical carcinoma,radiotherapy can reinforce the expression of FHIT protein. FHIT expression may be helpful in judgment of the radiosensitivity of cervical carcinoma.
出处 《现代妇产科进展》 CSCD 北大核心 2009年第10期731-733,共3页 Progress in Obstetrics and Gynecology
关键词 宫颈肿瘤 FHIT蛋白 基因 肿瘤抑制 放射疗法 Cervix neoplasms FHIT protein Genes, tumor suppressor Radiotherapy
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参考文献8

  • 1Hao XP, Willis JE, Pretlow TG, et al. Loss of fragile histidine triad expression in colorectal carcinomas and premalignant lesions[ J]. Cancer Res ,2000,60:1821-1823.
  • 2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
  • 3Huang LW, Chao SL, Chen TJ. Reduced Fhit expression in cervical carcinoma: correlation with tumor progression and poor prognosis [ J ]. Gynecol Oncol, 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 allelic imbalance at FHIT, RB1 and TP53 in relation to survival [ J ]. Int J Cancer,2000,88:217-222.
  • 5张文淼,王群姬,帅茨霞,朱华.FHIT基因表达异常或缺失与宫颈癌前病变及宫颈癌的关系[J].温州医学院学报,2005,35(1):31-33. 被引量:5
  • 6Sard L, Accornero P, Tornielli S, et al. The tumor suppressor gene FHIT is involved in the regulation of apoptosis and in the regulation of apoptosis and in cell cycle control [ J]. Proc Natl Acad Sci U S A, 1999,96:8489-8492.
  • 7Campiglio M, Bianchi F, Andriani F, et al. Diadenosines as FHIT-ness instructors [ J ]. J Cell Physio, 2006,208 : 274- 281.
  • 8郑虹,吴绪峰,陈惠祯.FHIT蛋白在宫颈癌中的表达及临床意义[J].数理医药学杂志,2004,17(3):216-218. 被引量:2

二级参考文献28

  • 1吕秀宁,郑杰.三氧化二砷诱导HeLa细胞凋亡与其抑制HPV18 E6表达和端粒酶活性有关[J].中华肿瘤杂志,2005,27(5):265-268. 被引量:16
  • 2Huang LW, Chao SL, Chen TJ. Redu ced Fhit expression in cervical carcinoma: correlation with tnmor progression and poor prognosis[J].Gynecol Oncol,2003,90(2) :331 - 337.
  • 3Helland A, Kraggerud SM, Kristensen GB, et al. Primary cervical carcinomas show 2 common regions of detion at 3p, 1 within the FHIT gene: evaluation of allelic imbalance at FHTT, RB1 and TP53in relation to survival[J]. Int J Cancer, 2000,88(2) :217 - 222.
  • 4Barnes LD, Garrison PN, SiprashviliZ, et al. Fhit, aputative mumor suppression in humans, is a dinucleoside 5-prime,5-triple prime-P(I),P(3)-triphosphate hydrolase[ J]. Biochemistry, 1996,35(36): 111529- 111535.
  • 5Tseng JE, Kemp BL, Khuri FR, et al. Loss of Fhit is frequent in stage 1 non-small cell lung cancer and in the lungs of chronic smokers[J].Cancer Res, 1999,59(19):4798-4803.
  • 6Wilke CM, Hall BK, HogeA,et al. RA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites [J].Hum Mol Genet, 1996,5(2): 187 - 195.
  • 7Wistuba l0, Montellano FD,Milchgrub S, et al. Deletions of chromosome 3p are frequent and early events in the pathogenesis of uterine cervical carcinoma[J]. Cancer Res, 1997,57(15) :3154 - 3158.
  • 8Connolly DC, Greenspan DL, Wu R, et al. Loss of fhit expression in invasive cervical carcinomas intraepithelial lesions associated with invasive disease[J].Clin Cancer Res, 2000,6(9):3505-3510.
  • 9Ji L, Fang B, Yen N, et al. Induction of apoptosis and inhibition of tumorigenicity and tumor growth by adenovirus vector-mediated fragile histidine triad (FHIT) gene overexpression. Cancer Res,1999, 59: 3333~3339.
  • 10Disaia PJ, Creasman WT. Clinical Gynecologic Oncology. 5th..st. Louis: Mosby, Inc. 1997: 85-99.

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