DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

Manel Esteller, Mario F. Fraga, Mingzhou Guo, Jesus Garcia-Foncillas, Ingrid Hedenfalk, Andrew K. Godwin, Joerg Trojan, Catherine Vaurs-Barriere, Yves-Jean Bignon, Susan Ramus, Javier Benitez, Trinidad Caldes, Yoshimitsu Akiyama, Yusuhito Yuasa, Virpi Launonen, Maria Jesus Canal, Roberto Rodriguez, Gabriel Capella, Miguel Angel Peinado, Åke BorgLauri A. Aaltonen, Bruce A. Ponder, Stephen B. Baylin, James G. Herman

Research output: Contribution to journalArticlepeer-review


Cancer cells have aberrant patterns of DNA methylation including hypermethylation of gene promoter CpG islands and global demethylation of the genome. Genes that cause familial cancer, as well as other genes, can be silenced by promoter hypermethylation in sporadic tumors, but the methylation of these genes in tumors from kindreds with inherited cancer syndromes has not been well characterized. Here, we examine CpG island methylation of 10 genes (hMLH1, BRCA1, APC, LKB1, CDH1, p16(INK4a), p14(ARF), MGMT, GSTP1 and RARbeta2) and 5-methylcytosine DNA content, in inherited (n = 342) and non-inherited (n = 215) breast and colorectal cancers. Our results show that singly retained alleles of germline mutated genes are never hypermethylated in inherited tumors. However, this epigenetic change is a frequent second "hit", associated with the wild-type copy of these genes in inherited tumors where both alleles are retained. Global hypomethylation was similar between sporadic and hereditary cases, but distinct differences existed in patterns of methylation at non-familial genes. This study demonstrates that hereditary cancers "mimic" the DNA methylation patterns present in the sporadic tumors.
Original languageEnglish
Pages (from-to)3001-3007
JournalHuman Molecular Genetics
Issue number26
Publication statusPublished - 2001

Subject classification (UKÄ)

  • Medical Genetics


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