Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers

Martina L. Veigl, Lakshmi Kasturi, Joseph Olechnowicz, Aihong Ma, James D. Lutterbaugh, Sumudra Periyasamy, Guo Min Li, James Drummond, Paul L. Modrich, W. David Sedwick, Sanford D. Markowitz

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Abstract

Mutations of DNA mismatch repair genes, including the hMLH1 gene, have been linked to human colon and other cancers in which defective DNA repair is evidenced by the associated instability of DNA microsatellite sequences (MSI). Germ-line hMLH1 mutations are causally associated with inherited MSI colon cancer, and somatic mutations are causally associated with sporadic MSI colon cancer. Previously however, we demonstrated that in many sporadic MSI colon cancers hMLH1 and all other DNA mismatch repair genes are wild type. To investigate this class of tumors further, we examined a group of MSI cancer cell lines, most of which were documented as established from antecedent MSI- positive malignant tumors. In five of six such cases we found that hMLH1 protein was absent, even though hMLH1-coding sequences were wild type. In each such case, absence of hMLH1 protein was associated with the methylation of the hMLH1 gene promoter. Furthermore, in each case, treatment with the demethylating agent 5-azacytidine induced expression of the absent hMLH1 protein. Moreover, in single cell clones, hMLH1 expression could be turned on, off, and on again by 5-azacytidine exposure, washout, and reexposure. This epigenetic inactivation of hMLH1 additionally accounted for the silencing of both maternal and paternal tumor hMLH1 alleles, both of which could be reactivated by 5-azacytidine. In summary, substantial numbers of human MSI cancers appear to arise by hMLH1 silencing via an epigenetic mechanism that can inactivate both of the hMLH1 alleles. Promoter methylation is intimately associated with this epigenetic silencing mechanism.

Original languageEnglish (US)
Pages (from-to)8698-8702
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume95
Issue number15
DOIs
StatePublished - Jul 21 1998

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Gene Silencing
Epigenomics
Microsatellite Repeats
Azacitidine
Colonic Neoplasms
Neoplasms
DNA Mismatch Repair
Methylation
Genes
Alleles
Microsatellite Instability
Mutation
Proteins
Germ-Line Mutation
DNA Repair
Clone Cells
Mothers
Cell Line

ASJC Scopus subject areas

  • General

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Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. / Veigl, Martina L.; Kasturi, Lakshmi; Olechnowicz, Joseph; Ma, Aihong; Lutterbaugh, James D.; Periyasamy, Sumudra; Li, Guo Min; Drummond, James; Modrich, Paul L.; Sedwick, W. David; Markowitz, Sanford D.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 95, No. 15, 21.07.1998, p. 8698-8702.

Research output: Contribution to journalArticle

Veigl, ML, Kasturi, L, Olechnowicz, J, Ma, A, Lutterbaugh, JD, Periyasamy, S, Li, GM, Drummond, J, Modrich, PL, Sedwick, WD & Markowitz, SD 1998, 'Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers', Proceedings of the National Academy of Sciences of the United States of America, vol. 95, no. 15, pp. 8698-8702. https://doi.org/10.1073/pnas.95.15.8698
Veigl, Martina L. ; Kasturi, Lakshmi ; Olechnowicz, Joseph ; Ma, Aihong ; Lutterbaugh, James D. ; Periyasamy, Sumudra ; Li, Guo Min ; Drummond, James ; Modrich, Paul L. ; Sedwick, W. David ; Markowitz, Sanford D. / Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. In: Proceedings of the National Academy of Sciences of the United States of America. 1998 ; Vol. 95, No. 15. pp. 8698-8702.
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AU - Lutterbaugh, James D.

AU - Periyasamy, Sumudra

AU - Li, Guo Min

AU - Drummond, James

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AU - Sedwick, W. David

AU - Markowitz, Sanford D.

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