MGMT hypermethylation: A prognostic foe, a predictive friend

被引:113
作者
Jacinto, Filipe V. [1 ]
Esteller, Manel [1 ]
机构
[1] Spanish Natl Canc Ctr CNIO, Mol Pathol Program, Canc Epigenet Lab, Madrid, Spain
关键词
MGMT hypermethylation; alkylation; DNA;
D O I
10.1016/j.dnarep.2007.03.013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Alkylation of DNA at the O-6-position of guanine is one of the most critical events leading to mutation, cancer, and cell death. O-6-alkylguanine-DNA alkyltransferase (AGT), also known as O-6-methylguanine-DNA methyltransferase (MGMT), is the DNA repair protein responsible for removing alkylation. adducts from the O-6-position of guanine in DNA. The promoter CpG island hypermethylation-associated gene silencing of MGMT is associated with a wide spectrum of human tumors. This epigenetic inactivation of MGMT has two main consequences in human cancer. First, it uncovers a new mutator pathway that causes the accumulation of G-to-A transition mutations that can affect genes required for genomic stability. Second, there is a strong and significant positive correlation between MGMT promoter hypermethylation and increased tumor sensitivity to alkylating drugs. These findings underline the importance of MGMT promoter hypermethylation in basic and translational cancer research. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1155 / 1160
页数:6
相关论文
共 55 条
  • [1] RAS GENES
    BARBACID, M
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 : 779 - 827
  • [2] DNA hypermethylation in tumorigenesis - epigenetics joins genetics
    Baylin, SB
    Herman, JG
    [J]. TRENDS IN GENETICS, 2000, 16 (04) : 168 - 174
  • [3] Belanich M, 1996, CANCER RES, V56, P783
  • [4] Human cancers express a mutator phenotype
    Bielas, Jason H.
    Loeb, Keith R.
    Rubin, Brian P.
    True, Lawrence D.
    Loeb, Lawrence A.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (48) : 18238 - 18242
  • [5] Brabender J, 2003, CLIN CANCER RES, V9, P223
  • [6] Cai YN, 1999, CANCER RES, V59, P3059
  • [7] DETECTION OF MESSENGER-RNA FROM O6-METHYLGUANINE-DNA METHYLTRANSFERASE GENE MGMT IN HUMAN NORMAL AND TUMOR-TISSUES
    CITRON, M
    GRAVER, M
    SCHOENHAUS, M
    CHEN, S
    DECKER, R
    KLEYNERMAN, L
    KAHN, LB
    WHITE, A
    FORNACE, AJ
    YAROSH, D
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (05) : 337 - 340
  • [8] COLVIN M, 1981, CANCER TREAT REP, V65, P89
  • [9] COSTELLO JF, 1994, J BIOL CHEM, V269, P17228
  • [10] GENETIC STUDIES OF LAC REPRESSOR .3. ADDITIONAL CORRELATION OF MUTATIONAL SITES WITH SPECIFIC AMINO-ACID RESIDUES
    COULONDRE, C
    MILLER, JH
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1977, 117 (03) : 525 - 567