Literature DB >> 15256060

Aberrant methylation of the maspin promoter is an early event in human breast cancer.

Bernard W Futscher1, Megan M O'Meara, Christina J Kim, Margaret A Rennels, Di Lu, Lynn M Gruman, Richard E B Seftor, Mary J C Hendrix, Frederick E Domann.   

Abstract

The maspin gene functions as a tumor suppressor in human breasts, and its expression is frequently lost during breast cancer progression. In vitro models of human breast cancer indicate that the loss of maspin expression is closely linked to aberrant methylation of the maspin promoter. We conducted a study on 30 archival ductal carcinoma in situ (DCIS) specimens to determine if aberrant methylation of the maspin promoter occurred in vivo, and whether it occurred early in breast cancer evolution. Healthy tissue obtained from reduction mammoplasty was used as normal control. Results from immunohistochemical analysis indicate that maspin expression is lost in a substantial fraction of DCIS specimens (57%). Bisulfite sequencing of DNA isolated from laser capture-microdissected normal and neoplastic ducts showed that loss of maspin expression was often, but not always, linked to aberrant methylation of the maspin promoter, suggesting that other mechanisms, in addition to aberrant methylation, participate and/or cooperate to silence maspin gene expression. Taken together, these results indicate that aberrant methylation of the maspin promoter is an early event in human breast cancer. Copyright 2004 Neoplasia Press, Inc.

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Year:  2004        PMID: 15256060      PMCID: PMC1502109          DOI: 10.1593/neo.04115

Source DB:  PubMed          Journal:  Neoplasia        ISSN: 1476-5586            Impact factor:   5.715


  38 in total

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Journal:  Placenta       Date:  2002-04       Impact factor: 3.481

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9.  Hypermethylation and histone deacetylation lead to silencing of the maspin gene in human breast cancer.

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Journal:  Breast Cancer Res       Date:  2002-05-16       Impact factor: 6.466

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  24 in total

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Review 4.  Writing and rewriting the epigenetic code of cancer cells: from engineered proteins to small molecules.

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5.  Methyl-binding domain protein 2-dependent proliferation and survival of breast cancer cells.

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7.  Quantitative methylation profiling in tumor and matched morphologically normal tissues from breast cancer patients.

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9.  Stepwise DNA methylation changes are linked to escape from defined proliferation barriers and mammary epithelial cell immortalization.

Authors:  Petr Novak; Taylor J Jensen; James C Garbe; Martha R Stampfer; Bernard W Futscher
Journal:  Cancer Res       Date:  2009-06-09       Impact factor: 12.701

Review 10.  Regulation of SOD2 in cancer by histone modifications and CpG methylation: closing the loop between redox biology and epigenetics.

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Journal:  Antioxid Redox Signal       Date:  2012-10-18       Impact factor: 8.401

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