5′-cytosine DNA-methyltransferase mRNA levels in hereditary colon carcinoma

被引:3
作者
Jakob, CA
Guldenschuh, I
Hürlimann, R
Müllhaupt, B
Müller, A
Ammann, R
Fried, M
Roth, J
机构
[1] Dept Pathol, Div Cell & Mol Biol, CH-8091 Zurich, Switzerland
[2] Univ Zurich Hosp, Dept Internal Med, Div Gastroenterol, CH-8091 Zurich, Switzerland
来源
VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY | 1999年 / 434卷 / 01期
关键词
mRNA quantification; RT-PCR; competitive RT-PCR; hereditary colon carcinoma; FAP; HNPCC;
D O I
10.1007/s004280050305
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
DNA methylation plays an important part in the regulation of gene expression. Alterations in DNA methylation in tumours have been reported and have been used to generate hypotheses about mutagenesis and silencing of tumour suppressor genes. However, the underlying mechanism is still poorly understood, and conflicting data on the levels of overexpression of 5'-cytosine DNA methyltransferase in sporadic colon carcinoma have been published. We used a competitive RT-PCR assay for quantification of mRNA of 5'-cytosine DNA methyltransferase in colon biopsies obtained from patients with hereditary colon carcinoma syndromes and compared the results with those obtained ill a control group. No significant difference was found between the flat mucose of FAP patients and the mucosa of the control group. In FAP and HNPCC patients, the 5'-cytosine DNA methyltransferase mRNA levels of adenomas were significantly higher (P<0.05) than of flat mucosa in the same group, but both showed great variability from patient to patient. Our findings suggest that the mRNA levels of methyltransferase cannot be used as predictive marker for screening in families affected by hereditary colon carcinoma.
引用
收藏
页码:57 / 62
页数:6
相关论文
共 46 条
[11]   STRAIGHTENING OUT THE BENDS IN CURVED DNA [J].
HAGERMAN, PJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1131 (02) :125-132
[12]  
Hiltunen MO, 1997, INT J CANCER, V70, P644, DOI 10.1002/(SICI)1097-0215(19970317)70:6<644::AID-IJC3>3.0.CO
[13]  
2-V
[14]   INCREASED CYTOSINE DNA-METHYLTRANSFERASE ACTIVITY DURING COLON-CANCER PROGRESSION [J].
ISSA, JPJ ;
VERTINO, PM ;
WU, JJ ;
SAZAWAL, S ;
CELANO, P ;
NELKIN, BD ;
HAMILTON, SR ;
BAYLIN, SB .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (15) :1235-1240
[15]  
Iwama T, 1977, Jpn J Surg, V7, P230, DOI 10.1007/BF02469355
[16]  
JIRICNY J, 1998, IN PRESS EMBO J
[17]   Lessons from hereditary colorectal cancer [J].
Kinzler, KW ;
Vogelstein, B .
CELL, 1996, 87 (02) :159-170
[18]   Oncogenic mechanisms mediated by DNA methylation [J].
Laird, PW .
MOLECULAR MEDICINE TODAY, 1997, 3 (05) :223-229
[19]   The role of DNA methylation in cancer genetics and epigenetics [J].
Laird, PW ;
Jaenisch, R .
ANNUAL REVIEW OF GENETICS, 1996, 30 :441-464
[20]   SUPPRESSION OF INTESTINAL NEOPLASIA BY DNA HYPOMETHYLATION [J].
LAIRD, PW ;
JACKSONGRUSBY, L ;
FAZELI, A ;
DICKINSON, SL ;
JUNG, WE ;
LI, E ;
WEINBERG, RA ;
JAENISCH, R .
CELL, 1995, 81 (02) :197-205