Journal
CURRENT OPINION IN GASTROENTEROLOGY
Volume 24, Issue 5, Pages 597-602Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MOG.0b013e32830b111d
Keywords
chromatin-modifying proteins; epigenetics; heterochromatin protein 1; pancreatic cancer; polycomb
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Funding
- NIDDK NIH HHS [R01 DK052913-10A2, R01 DK052913] Funding Source: Medline
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Purpose of review The excitement of finding a cancer modulator which is either mutated or deleted in vivo (genetics), unfortunately, is shadowed by the fact that we scientists have failed to live to the promise of gene therapy, and therefore, these genes cannot be replaced to cure the patients. On the contrary, both DNA methylation and chromatin-mediated inactivation of tumor suppressor genes (epigenetics), for example, are reversible as demonstrated by the relative success of emerging therapies. Therefore, epigenetics with its molecular basis (DNA methylation and chromatin modification) is among the most promising areas of cancer research and is a nascent field in pancreatic cancer research. Recent findings Here, we review and update novel findings on epigenetics as it applies to pancreatic cancer. Summary Special focus has been given to novel potential therapeutic targets and currently available drugs, which are emerging from this exciting new field of pancreatic cancer research.
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