AI Article Synopsis

  • The review focuses on epigenetic changes in ovarian cancer, particularly their potential as clinical markers for detection and disease monitoring.
  • These changes include genome-wide demethylation and hypermethylation of specific genes, highlighting the significance of DNA methylation alterations in early cancer development.
  • The identification of these epigenetic changes opens up possibilities for non-invasive detection methods and improved patient stratification in targeted therapies.

Article Abstract

Objective: To review epigenetic changes identified in ovarian cancer, focusing on their potential as clinical markers for detection, monitoring of disease progression and as markers of therapeutic response.

Methods: A comprehensive review of English language scientific literature on the topics of methylation and ovarian cancer was conducted.

Results: Genome-wide demethylation of normally methylated and silenced chromosomal regions, and hypermethylation and silencing of genes including tumor suppressors are common features of cancer cells. Epigenetic alterations, including CpG island DNA methylation, occur in ovarian cancer and the identification of specific genes that are altered by epigenetic events is an area of intense research. Aberrant DNA methylation in ovarian cancer is observed in early cancer development, can be detected in DNA circulating in the blood and hence provides the promise of a non-invasive cancer detection test. In addition, identification of ovarian cancer-specific epigenetic changes has promise in molecular classification and disease stratification.

Conclusions: The detection of cancer-specific DNA methylation changes heralds an exciting new era in cancer diagnosis as well as evaluation of prognosis and therapeutic responsiveness and warrants further investigation.

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Source
http://dx.doi.org/10.1016/j.ygyno.2007.12.017DOI Listing

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