Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/82359
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Type: Journal article
Title: Common gene pathways and families altered by DNA methylation in breast and prostate cancers
Author: Day, T.
Bianco-Miotto, T.
Citation: Endocrine-Related Cancer, 2013; 20(5):215-232
Publisher: Soc Endocrinology
Issue Date: 2013
ISSN: 1351-0088
1479-6821
Statement of
Responsibility: 
Tanya K Day and Tina Bianco-Miotto
Abstract: Epigenetic modifications, such as DNA methylation, are widely studied in cancer as they are stable and easy to measure genome wide. DNA methylation changes have been used to differentiate benign from malignant tissue and to predict tumor recurrence or patient outcome. Multiple genome wide DNA methylation studies in breast and prostate cancers have identified genes that are differentially methylated in malignant tissue compared with non-malignant tissue or in association with hormone receptor status or tumor recurrence. Although this has identified potential biomarkers for diagnosis and prognosis, what is highlighted by reviewing these studies is the similarities between breast and prostate cancers. In particular, the gene families/pathways targeted by DNA methylation in breast and prostate cancers have significant overlap and include homeobox genes, zinc finger transcription factors, S100 calcium binding proteins, and potassium voltage-gated family members. Many of the gene pathways targeted by aberrant methylation in breast and prostate cancers are not targeted in other cancers, suggesting that some of these targets may be specific to hormonal cancers. Genome wide DNA methylation profiles in breast and prostate cancers will not only define more specific and sensitive biomarkers for cancer diagnosis and prognosis but also identify novel therapeutic targets, which may be direct targets of agents that reverse DNA methylation or which may target novel gene families that are themselves DNA methylation targets.
Keywords: breast; prostate; biomarker; gene regulation; neoplasia
Rights: © 2013 Society for Endocrinology
RMID: 0020135919
DOI: 10.1530/ERC-13-0204
Appears in Collections:Medicine publications

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