期刊文献+

6-氧-甲基鸟嘌呤-DNA甲基转移酶和P53在人脑胶质瘤中的表达与病理级别和预后关系的研究 被引量:2

The Correlation of the Expression of MGMT and P53 in Human Brain Gliomas with Tumor Grade or Prognosis
原文传递
导出
摘要 目的:探讨6-氧-甲基鸟嘌呤-DNA甲基转移酶(MGMT)和P53在脑胶质瘤中的表达及意义。方法:采用免疫组化法检测133例肿瘤组织中MGMT蛋白和P53蛋白的表达情况,分析MGMT和P53与胶质瘤临床病理特征、预后及两者之间的相互关系。结果:不同级别胶质瘤间MGMT阳性表达率差异无统计学意义(P=0.158);MGMT阳性表达水平差异也无统计学意义(P=0.138),但MGMT表达水平与患者生存时间密切相关(P=1.07×10-6)。不同级别胶质瘤间P53阳性表达率差异无统计学意义(P=0.306),而表达水平则在胶质瘤不同级别间差异有显著统计学意义,且呈正相关关系(r=0.187,P=0.032);P53表达水平与患者生存时间密切相关(P=2.08×10-14);MGMT和P53间无相关性(P=0.065)。结论:MGMT蛋白表达与胶质瘤病理分级无明显关系,P53蛋白表达水平与胶质瘤病理分级有关,两者都与生存时间密切相关。 Aim: To explore the correlation of the expression of O6-methylguanine-DNA methyltransferase(MGMT) and P53 in human brain gliomas with tumor grade or prognosis.Methods: The expression of MGMT and P53 in glioma tissues from 133 cases was detected using immunohistochemistry methods and its correlation with tumor grade or prognosis was also analyzed.Results: ① There was no statistically significant difference between the expression of MGMT or its intensity in different grades of gliomas(P=0.158,0.138,respectively) and the survival rates decreased with the increase of intensity of MGMT expression by Kaplan-Meier survival curve(P=1.07 × 10-6).② There was no statistically significant difference between the expression of P53 in different grades of gliomas(P=0.306),but the intensity of P53 expression was statistically significant different(P=0.032) and showed positive correlation(r=0.187).The survival rates decreased with the increase of intensity of P53 expression by Kaplan-Meier survival curve(P=2.08 × 10-14).③ There was no statistically significant difference between the intensity of MGMT expression and the intensity of P53 expression(P=0.065).Conclusion: Our findings suggested that the expression of MGMT was correlated with glioma patient survival,not with tumor grade.The expression of P53 was not related to tumor grade.However,the intensity of P53 expression increased with the tumor grade,and was reversely associated with the survival time of patients.
作者 季列 周范民
出处 《中国临床神经科学》 2011年第6期588-593,共6页 Chinese Journal of Clinical Neurosciences
关键词 胶质瘤 6-氧-甲基鸟嘌呤-DNA甲基转移酶 P53 病理 预后 glioma O6-methylguanine-DNA methyltransferase P53 pathology prognosis
  • 相关文献

参考文献21

  • 1Hegi ME, Diserens AC, Gorlia T, et al. MGMT gene silencing and benefit from temozolomide in glioblastoma[J]. N Engl J Med, 2005, 352:997-1003.
  • 2Shiraishi S, Tada K, Nakamura H, et al. Influence of p53 mutations on prognosis of patients with glioblastoma[J]. Cancer,2002,95: 249-257.
  • 3Kleihues P, Cavenee WK. WHO classification of tumors, pathol- ogy and genetics of tumors of the nervous system[M]. Lyon: IARC Pre,2000:1-253.
  • 4刘淑慧,吴贤英,李乔山,郑瑞明.免疫组织化学染色检测食管组织MGMT和P53蛋白的表达及其相关性[J].现代医院,2008,8(7):18-20. 被引量:3
  • 5Gerson SL, Trey JE, Miller K, et al. Comparison of O6-alkylguanine- DNA alkyltransferase activity based on cellular DNA content in human, rat and mouse tissues[J]. Carcinogenesis,1986,7:745-749.
  • 6Pulling LC, Divine KK, Klinge DM, et al. Promoter hypermethyla- tion of the 06-methylguanine-DNA methyltransferase gene:more common in lung adenocarcinomas from never-smokers thansmokers and associated with tumor progression[J]. Cancer Res, 2003,63:4842-4848.
  • 7孙彦辉,张亚卓,王忠诚,孙梅珍,赵东海.MGMT在脑胶质瘤组织中的表达及其与患者生存期的关系[J].癌症,2004,23(9):1052-1055. 被引量:36
  • 8Brell M, Tortosa A, Verger E, et al. Prognostic significance of 06- methylguanine-DNA methyltransferase determined by promoter hypermethylation and immunohistochemical expression in ana- plastic gliomas[J]. Clin Cancer Res,2005,11:5167-5174.
  • 9Nakasu S, Fukami T, Jito J, et al. Prognostic significance of loss of O6-methylguanine-DNA methyltransferase expression in supratentorioal diffuse low-grade astrocytoma[J]. Surg Neurol, 2007,68:603-608.
  • 10Sidransky D, Mikkelsen T, Schwechheimer K, et al. Clonal expan- sion of p53 mutant cells is associated with brain tumour progression [J]. Nature, 1992,355:846-847.

二级参考文献25

  • 1张天华,邹小明,刘建丰,曹守强.MGMT蛋白在胃癌中的表达及其临床意义[J].中国普通外科杂志,2005,14(3):225-227. 被引量:13
  • 2Balana C, Ramirez JL, Taron M, et al. O6 methylguanine DNA methyltransferase Methylation in Serum and Tumor DNA Predicts Response to 1,3 Bis(2 Chloroethyl) 1 Nitrosourea but not to Temozolamide Plus Cisplatin in Glioblastoma Multiforme [J]. Clin Cancer Res, 2003, 9(4): 1461- 1468.
  • 3Andratachke N, Grosu AL, Molls M, et al. Perspectives in the treament of malignant gliomas in adults [J]. Anticancer Res, 2001, 21(5):3541- 3550.
  • 4Silber JR, Bobola MS, Ghatan S, et al. O6 methylguanine DNA methyltransferase activity in adult gliomas: relation to patient and tumor characteristics [J]. Cancer Res, 1998, 58(5): 1068- 1073.
  • 5Silber JR, Blank A, Bobola MS, et al. O6 methylguanine DNA methltransferase deficient phenotype in human gliomas: frequency and time to tumor progression after alkylating agent based chemotherapy [J]. Clin Cancer Res, 1999, 5(4): 807- 814.
  • 6Nutt CL, Loktionova NA, Pegg AE, et al. O(6) methylguanine DNA methyltransferase activity, p53 gene status and BCNU resistance in mouse astrocytes [J]. Carcinogenesis, 1999, 20(12): 2361- 2365.
  • 7Bobola MS, Berger MS, Ellenbogen RG, et al. O6 Methylguanine DNA methyltransferase in pediatric primary brain tumors: relation to patients and tumor characteristics [J]. Clin Cancer Res,2001,7(3):613- 619.
  • 8Esteller M, Garcia Foncillas J, Andion E, et al. Inactivation of the DNA Repair Gene MGMT and the Clinical Response of Gliomas to Alkylating Agents [J]. N Engl J Med, 2000, 343(23):1350- 1354.
  • 9Watanabe T, Nakamura M, Kros JM, et al. Phenotype versus genotype correlation in oligodendrogliomas and low grade diffuse astrocytomas [J]. Acta Neuropathol (Berl), 2002,103(3):267- 275.
  • 10Nakamura M, Watanabe T, Yonekawa Y, et al. Promoter methylation of the DNA repair gene MGMT in astrocytomas is frequently associated with G:C→ A:T mutations of the TP53 tumor suppressor gene [J]. Carcinogenesis, 2001, 22(10):1715- 1719.

共引文献37

同被引文献22

  • 1孙彦辉,张亚卓,王忠诚,孙梅珍,赵东海.MGMT在脑胶质瘤组织中的表达及其与患者生存期的关系[J].癌症,2004,23(9):1052-1055. 被引量:36
  • 2林英,郝卓芳,黄世章,廖德贵.DNA修复酶MGMT和Ki-67抗原在脑胶质瘤中的表达及其意义[J].广东医学,2005,26(8):1063-1065. 被引量:1
  • 3王树森,管忠震,向燕群,汪波,林桐榆,姜文奇,张力,张惠忠,侯景辉.鼻咽癌组织中EGFR和p-ERK蛋白表达的检测及意义[J].中华肿瘤杂志,2006,28(1):28-31. 被引量:47
  • 4董伦,浦佩玉,王虎,王广秀,康春生,焦德让.EGFR、p53与Ki-67在国人胶质瘤中表达研究[J].中华神经外科杂志,2006,22(7):442-444. 被引量:9
  • 5Ikeguchi M,Makino M,Kaibara N. Telomerase activity and p53 genemutation in familial polyposis coil [ J ]. Anticancer Res,2000,20(5c): 3833-3837.
  • 6Hegi ME, Diserens A-C,Gorlia T,et al. MGMT gene silencing andbenefit from temozolomide in glioblastoma[ J]. N Engl J Med, 2005,325(10) : 997-1003.
  • 7Yuan Q, Matsumoto K, Nakabeppu Y, et al. A comparative immuno-histochemistry of 0 6 -methylguanine-DNA methyltransferase and p53 indiffusely infiltrating aslroylomas [ J ] Neuropathology,2003,23(3) : 203.
  • 8Roger S,Monika EH, Warren PM, et al. Effects of radiotherapy withconcom itant and adjuvant temozolomide versus radiotherepy alone onsurvival in glioblastoma in randomized phase III study 5 -year analysisof the EORTC-NCIC trial[J]. Lancet Oncol ,2009,10 (11) :459466.
  • 9Meert A P, Martin B, Delmotte P, et al. The role of EGFR expressionon patient survival in lung cancer: a systematic review with meta-anal-ysis[ J]. Eur Respir J, 2002 , 20(4) : 975-981.
  • 10Blough MDt zlatescu MC, Caimcross JG, et al. O6 - methylguanine-DNA methyltransferase regulation by p53 in astrocytic cell[ J]. Cancer.

引证文献2

二级引证文献15

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