O6-methylguanine-DNA methyltransferase promoter hypermethylation in colorectal carcinogenesis

被引:0
|
作者
Menigatti, Mirco
Pedroni, Monica
Verrone, Anna Maria
Borghi, Francesca
Scarselli, Alessandra
Benatti, Piero
Losi, Lorena
Di Gregorio, Carmela
Schar, Primo
Marra, Giancarlo
De Leon, Maurizio Ponz
Roncucci, Luca
机构
[1] Univ Basel, DKBW, Dept Biol Clin Sci, Ctr Biomed, CH-4058 Basel, Switzerland
[2] Univ Modena, Dept Internal Med, I-41100 Modena, Italy
[3] Univ Modena, Dept Pathol, I-41100 Modena, Italy
[4] Univ Modena, Div Med Oncol, Dept Hematol & Oncol, I-41100 Modena, Italy
[5] Osped Carpi, Dept Pathol, Carpi, Italy
[6] Univ Zurich, Inst Mol Canc Res, Zurich, Switzerland
关键词
aberrant Crypt foci; O-6-methylguanine-DNA methyltransferase promoter hypermethylation; colorectal cancer; colorectal carcinogenesis; K-ras mutation;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epigenetic alterations have been reported in colorectal neoplasia which can either complement or in some cases be predisposed to genetic alterations such as K-ras mutations. We examined the promoter methylation status of the CDKN2A and O-6-methylguanine-DNA methyltransferase (MGMT) genes, after sodium bisulfite conversion and DNA amplification with methylation specific PCR. Moreover, we searched for G to A transitions in codons 12 and 13 of the K-ras oncogene in normal colorectal mucosae, aberrant crypt foci (ACF, early premalignant lesions) and carcinomas. CDKN2A hypermethylation was an infrequent event in ACF (2 of 26, 7.7%). On the contrary, MGMT hypermethylation was found in the normal mucosae (3 of the 12 samples, 25%), in 14 of the 26 ACF (53.8%) and in 7 of the 9 (77.8%) carcinomas examined. K-ras mutations were evident in 6 ACF (23%) and in 3 carcinomas (33.3%), mostly associated with MGMT promoter hypermethylation. These findings strongly support the hypothesis that epigenetic mechanisms play an important role in the early steps of colorectal carcinogenesis.
引用
收藏
页码:1421 / 1427
页数:7
相关论文
共 50 条
  • [1] Promoter hypermethylation of O6-methylguanine-DNA methyltransferase gene in gliomas
    Ohgaki, H
    Nakamura, M
    Watanabe, T
    Kleihues, P
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2001, 60 (05): : 534 - 534
  • [2] Persistent organic pollutants and promoter hypermethylation of the O6-methylguanine-DNA methyltransferase gene
    Park, Soo Yeun
    Kim, Ki-Su
    Lee, Yu-Mi
    Kim, Mi-Jin
    Jacobs, David R., Jr.
    Porta, Miquel
    Kim, Dong-Sun
    Lee, Duk-Hee
    BIOMARKERS, 2015, 20 (02) : 136 - 142
  • [3] Inactivation of O6-methylguanine-DNA methyltransferase by promoter CpG island hypermethylation in gastric cancers
    Bae, SI
    Lee, HS
    Kim, SH
    Kim, WH
    BRITISH JOURNAL OF CANCER, 2002, 86 (12) : 1888 - 1892
  • [4] Inactivation of O6-methylguanine-DNA methyltransferase by promoter CpG island hypermethylation in gastric cancers
    S I Bae
    H S Lee
    S H Kim
    W H Kim
    British Journal of Cancer, 2002, 86 : 1888 - 1892
  • [5] Frequent promoter hypermethylation of the O6-methylguanine-DNA methyltransferase (MGMT) gene in testicular cancer
    Smith-Sorensen, B
    Lind, GE
    Skotheim, RI
    Fosså, SD
    Fodstad, O
    Stenwig, AE
    Jakobsen, KS
    Lothe, RA
    ONCOGENE, 2002, 21 (57) : 8878 - 8884
  • [6] Hypermethylation of O6-methylguanine-DNA methyltransferase promoter may predict nonrecurrence after chemotherapy in colorectal cancer cases
    Nagasaka, T
    Sharp, GB
    Notohara, K
    Kambara, T
    Sasamoto, H
    Isozaki, H
    MacPhee, DG
    Jass, JR
    Tanaka, N
    Matsubara, N
    CLINICAL CANCER RESEARCH, 2003, 9 (14) : 5306 - 5312
  • [7] Hypermethylation of O6-methylguanine-DNA methyltransferase promoter as a good predictor for colorectal cancer patients receiving chemotherapy.
    Matsubara, N
    Nagasaka, T
    Sharp, GB
    Notohara, K
    Baba, S
    Jass, JR
    Tanaka, N
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2002, 11 (10) : 1150S - 1151S
  • [8] O6-methylguanine-DNA methyltransferase (MGMT) promoter hypermethylation in neoplastic and normal mucosa in patients with colorectal carcinoma(CRC)
    Stravoravdi, P.
    Pailkos, D.
    Voyatzi, S.
    Tragiannidis, D.
    Soufleris, K.
    Pilpilidis, J.
    Tarpangos, A.
    Katsos, J.
    EJC SUPPLEMENTS, 2008, 6 (09): : 89 - 89
  • [9] Prognostic significance of O6-methylguanine-DNA methyltransferase determined by promoter hypermethylation and immunohistochemical expression in anaplastic gliomas
    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
  • [10] Inactivation of the DNA repair gene O6-methylguanine-DNA methyltransferase by promoter hypermethylation is associated with G to A mutations in K-ras in colorectal tumorigenesis
    Esteller, M
    Toyota, M
    Sanchez-Cespedes, M
    Capella, G
    Peinado, MA
    Watkins, DN
    Issa, JPJ
    Sidransky, D
    Baylin, SB
    Herman, JG
    CANCER RESEARCH, 2000, 60 (09) : 2368 - 2371