THE CORRELATION AND PROGNOSTIC SIGNIFICANCE OF MGMT PROMOTER METHYLATION AND MGMT PROTEIN IN GLIOBLASTOMAS

被引:102
作者
Cao, Van Thang [1 ,2 ]
Lung, Tae-Young [1 ,2 ,3 ]
Jung, Shin [1 ,2 ,3 ]
Jin, Shu-Guang [1 ,2 ]
Moon, Kyung-Sub [1 ,2 ,3 ]
Kim, In-Young [1 ,2 ,3 ]
Kang, Sam-Suk [3 ]
Park, Chang-Soo [4 ]
Lee, Kyung-Hwa [4 ]
Chae, Hong-Jae [5 ]
机构
[1] Chonnam Natl Univ, Hwasun Hosp & Med Sch, Brain Tumor Res Lab, Kwangju, South Korea
[2] Chonnam Natl Univ, Hwasun Hosp & Med Sch, Res Inst Med Sci, Kwangju, South Korea
[3] Chonnam Natl Univ, Hwasun Hosp & Med Sch, Dept Neurosurg, Kwangju, South Korea
[4] Chonnam Natl Univ, Hwasun Hosp & Med Sch, Dept Pathol, Kwangju, South Korea
[5] Chonnam Natl Univ, Hwasun Hosp & Med Sch, Dept Occupat & Environm Med, Kwangju, South Korea
关键词
Chemotherapy; Glioblastoma; Immunohistochemistry; MGMT promoter methylation; MGMT protein; DNA-REPAIR GENE; CPG ISLAND HYPERMETHYLATION; O-6-METHYLGUANINE-DNA METHYLTRANSFERASE; INACTIVATION; MUTATIONS; SURVIVAL; EXPRESSION; GLIOMA; IMMUNOHISTOCHEMISTRY; TUMORIGENESIS;
D O I
10.1227/01.NEU.0000357325.90347.A1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: The aim of this study was to evaluate the correlation and prognostic significance of MGMT promoter methylation and protein expression in patients with glioblastoma. METHODS: Eighty-three patients with glioblastoma underwent surgery followed by radiotherapy and temozolomide chemotherapy between October 2000 and June 2008. To investigate the correlation between MGMT methylation and MGMT expression, methylation-specific polymerase chain reaction (MSP) and immunohistochemical staining was performed. To analyze the correlation between MGMT methylation and MGMT expression according to location, biopsies were obtained from 37 different sites within the tumors in 12 patients. Age, sex, Karnofsky Performance Scale status, extent of removal, chemotherapeutic methods, and MGMT promoter methylation and protein expression were analyzed as prognostic factors. RESULTS: The total median survival was 15.8 months (range, 12.6-19.1 months). The results of MSP were the same at various sites in 12 patients. A correlation between MSP and immunohistochemical staining was observed in 50% of the patients. In 73 patients, negative MGMT expression was detected in 70.5% of 44 patients with MGMT promoter methylation, and positive expression was observed in 55.2% of the 29 patients with unmethylated promoters. Multivariate analysis revealed that the extent of removal (P = 0.001) and the combination of MGMT promoter methylation and negative MGMT expression (median survival, 20.06 months; P = 0.006) were significantly associated with longer survival. CONCLUSION: We report the feasibility of using MSP combined with immunohistochemical staining as a prognostic factor. The results of the present study suggest that MGMT promoter methylation in combination with negative MGMT expression might be a good prognostic factor in patients with glioblastoma.
引用
收藏
页码:866 / 875
页数:10
相关论文
共 47 条
[1]  
Afra D, 2002, LANCET, V359, P1011
[2]   Mice over-expressing human O6alkylguanine-DNA alkyltransferase selectively reduce O6methylguanine mediated carcinogenic mutations to threshold levels after N-methyl-N-nitrosourea [J].
Allay, E ;
Veigl, M ;
Gerson, SL .
ONCOGENE, 1999, 18 (25) :3783-3787
[3]   EFFECT OF THE EXTENT OF SURGICAL RESECTION ON SURVIVAL AND QUALITY-OF-LIFE IN PATIENTS WITH SUPRATENTORIAL GLIOBLASTOMAS AND ANAPLASTIC ASTROCYTOMAS [J].
AMMIRATI, M ;
VICK, N ;
LIAO, Y ;
CIRIC, I ;
MIKHAEL, M .
NEUROSURGERY, 1987, 21 (02) :201-206
[4]   Inactivation of O6-methylguanine-DNA methyltransferase by promoter CpG island hypermethylation in gastric cancers [J].
Bae, SI ;
Lee, HS ;
Kim, SH ;
Kim, WH .
BRITISH JOURNAL OF CANCER, 2002, 86 (12) :1888-1892
[5]   DNA hypermethylation in tumorigenesis - epigenetics joins genetics [J].
Baylin, SB ;
Herman, JG .
TRENDS IN GENETICS, 2000, 16 (04) :168-174
[6]   CpG methylation-dependent repression of the human O6-methylguanine-DNA methyltransferase gene linked to chromatin structure alteration [J].
Bhakat, KK ;
Mitra, S .
CARCINOGENESIS, 2003, 24 (08) :1337-1345
[7]   Regulation of the human O6-methylguanine-DNA methyltransferase gene by transcriptional coactivators cAMP response element-binding protein-binding protein and p300 [J].
Bhakat, KK ;
Mitra, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (44) :34197-34204
[8]   Correlation of clinical features and methylation status of MGMT gene promoter in glioblastomas [J].
Blanc, JL ;
Wager, M ;
Guilhot, J ;
Kusy, S ;
Bataille, B ;
Chantereau, T ;
Lapierre, F ;
Larsen, CJ ;
Karayan-Tapon, L .
JOURNAL OF NEURO-ONCOLOGY, 2004, 68 (03) :275-283
[9]   O6-methylguanine-DNA methyltransferase regulation by p53 in astrocytic cells [J].
Blough, Michael D. ;
Zlatescu, Magdalena C. ;
Cairncross, J. Gregory .
CANCER RESEARCH, 2007, 67 (02) :580-584
[10]   Prognostic significance of O6-methylguanine-DNA methyltransferase determined by promoter hypermethylation and immunohistochemical expression in anaplastic gliomas [J].
Brell, M ;
Tortosa, A ;
Verger, E ;
Gil, JM ;
Viñolas, N ;
Villá, S ;
Acebes, JJ ;
Caral, L ;
Pujol, T ;
Ferrer, I ;
Ribalta, T ;
Graus, F .
CLINICAL CANCER RESEARCH, 2005, 11 (14) :5167-5174