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MGMT在人脑胶质瘤中的表达及其临床意义 被引量:1

Expression of Drug Fast Enzyme MGMT in Human Brain Gliomas and Its Clinical Significance
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摘要 目的探讨耐药酶O6甲基鸟嘌呤-DNA-甲基转移酶(MGMT)在人脑胶质瘤中的表达及其临床意义。方法通过免疫组织化学方法检测60例脑胶质瘤患者MGMT蛋白表达情况,分析其与WHO分级的关系;同时对MG-MT表达为阳性的40例患者,分别采用化疗药物TMZ和CCNU进行化疗,观察比较两组的有效率、控制率。结果根据WHO分级,MGMT蛋白在Ⅰ~Ⅳ的阳性表达率分别为37.5%、66.7%、78.6%和100.0%。经χ2趋势检验,各等级之间差异有统计学意义(P<0.05)。通过强化CT或增强MRI判断病灶变化情况,TMZ组有效率(CR+PR)为22.7%,CC-NU组有效率为5.6%,两组差异有统计学意义(P<0.05)。TMZ组控制率(CR+PR+MR)为59.1%,CCNU组控制率为16.7%,两组差异有统计学意义(P<0.05)。结论MGMT表达对判定肿瘤的恶性程度对于制定化疗方案有重要参考价值,TMZ较CCNU更适用于MGMT表达阳性恶性脑胶质瘤的治疗。 Objective To investigate the expression of drug fast enzyme MGMT in human brain gliomas and its clinical chemotherapy value. Methods MGMT expression in 60 glioma specimens was examined by immunohistochemistry method, then the association of MGMT expression and WHO classification was analyzed. Meanwhile, 40 patients with MGMT positive expression were divided into two groups and given TMZ and OCNU respectively, the effective rate and the control rate were observed. Results According to WHO classification, MGMT positive expression in grade Ⅰ~Ⅳ were 37.5 %, 66.7%, 78.6%, and 100.0 %, respectively. Using Xz trend test, there was a statistically significant difference among each grade (P 〈 0.05). After contrast- enhanced CT or GD- MRI examination, the response rate was 22.7 % in TMZ group, and .5.6 % in CCNU group; the two groups had statistically significant differences (P〈 0.05). The control rate was 59.1% in TMZ group and 16.7 % in CCNU group, there were statistically significant differences between the two groups (P〈 0.0.5). Conclusions It is significant to detect MGMT expression simultaneously when judging the malignant degree of glioma and selecting chemotherapeutic plan for an individual patient. Comparing with CCNU, TMZ is more suitable for patients with MGMT positive expression.
出处 《实用预防医学》 CAS 2009年第2期506-508,共3页 Practical Preventive Medicine
关键词 O^6 甲基鸟嘌呤-DNA-甲基转移酶 脑胶质瘤 耐药性 MGMT Gliomas Drug resistance
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  • 1张俊英,陈忠平.MGMT基因表达与人脑胶质瘤化疗耐药关系研究[J].中国神经肿瘤杂志,2003,1(4):200-204. 被引量:12
  • 2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
  • 3林英,黄世章,郝卓芳,廖德贵.MGMT及P53在脑胶质瘤组织中的表达及其生物学意义[J].现代临床医学生物工程学杂志,2005,11(3):187-189. 被引量:8
  • 4曾宪起,申长虹,浦佩玉,杨树源.应用替莫唑胺对照司莫司丁治疗恶性脑胶质瘤的疗效观察[J].中华神经外科杂志,2006,22(4):204-207. 被引量:50
  • 5奥斯伯F 金斯顿RE 赛德曼JG 等主编 颜子颖 王海林译.精编分子牛物学实验指南:第1版[M].北京:科学出版社,1998.274-328.
  • 6[1]Monika E,Hegi Ph D,Annie-Claire Diserens,et al.MGMT gene silencing and benefit from temozolomide in glioblastoma[J].N Engl J Med,2005,352(10):997-1003.
  • 7[4]Iris Lavon,Dana Fuchs,Daniel Zrihan,et al.Novel mechanism whereby nuclear factor kappa B mediates DNA damage repair through regulation of O(6)-methylguanine-DNA-methyltransferase[J].Cancer Res,2007,67(18):8952-8959.
  • 8[5]Esteller 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.
  • 9[6]Yuan Q,Matsumoto K,Nakabeppu Y,et al.A comparative immunohisto-chemistry of O6-methylguanine-DNA methyltransferase,and p53 in diffusely infiltrating astrocytomas[J].Neuropathology,2003,23(3):203-209.
  • 10[8]Olivier S,Robe P,Bours V,et al.Can NF-kappa B be a target for novel and efficient anti-cancer agents[J].Biochem Pharmacol,2006,72(9):1054-1068.

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  • 1Hargrave DR, Zacharoulis S. Pediatric CNS tumors: cun'ent treatment and future directions[J]. Expert Rev Neurother,2007,7(8) : 1 029 - 1 042.
  • 2Chamberlain MC. Treatment options for glioblastoma [ J ]. Neurosurg Focus, 2006,20(4) :El9.
  • 3Westphal M, Hilt DC, Bortey E, et aI, A phase 3 trial of local chemotherapy with biodegradable carnustine(BCNU) wafers (Gliadel wafers) in patients with primary malignant glioma [ J ]. Neuro Oncol, 2003,5 ( 2 ) : 79 - 88.
  • 4Tano K, Shiota S, Collier J, et al. Isolation and structural characterization of a cDNA clone encoding the human DNA repair protein for 0^6 - alkylgua- nine[J]. Proc Natl Acad Sci USA, 1990,87(2) :686 - 690.
  • 5Dolan ME, Schilsky RL. Silence is golden : gene hypermethylation and survival in large - cell lymphoma[ J]. Ji Natl Cancer lnst,2002,94(1 ) :6 - 7.
  • 6Schilsky RL, Dolan ME, Bertucci D, et al. Phaselclinical and pharmaeolog- ical study of 06 -benzylguanine followed by carmustine in patients with advanced cancer[J]. Clin Caner Res,2000,6(8) :3 025 - 3 031.
  • 7Belanich M, Randall T, Pastor MA, et al. Intracellular localization and Intra- cellular hereogeneity of the human DNA repair protein 06 - methylguanine - DNA methyltransferase [ J ]. Cance:r Chemother Pharmacol, 1996,37 (6) : 547 - 555.
  • 8Esteller M, Gareia - Foncillas J, Andion E, et al. Inactivation of the DNA - repair gene MGMT and the clinical response of gliomas to alklating a- gents[J]. N Engl J Med,2000,343(19) :1 350 - 1 354.
  • 9Gerson SL, Trey JE, Miller K, el al. Comparison of 0^6 - alkylguanine - DNA alkyltransferase activity based on cellular DNA content in human, rat and mouse tisssues [J]. Carcinogenesis, 1986,7 (5) : 745 - 749.

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