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Epigenetic biomarkers in the diagnosis of ovarian cancer

, , & , MD PhD (Professor and Head)
Pages 421-438 | Published online: 24 Jun 2012
 

Abstract

Introduction: Current diagnostic methods for ovarian cancer have limited performance. Recent advances within the field of epigenetics have shifted the clinical implementation of epigenetic biomarkers as a diagnostic approach from a dream for the future to a present-day consideration. Patients could potentially benefit greatly from this novel diagnostic approach.

Areas covered: Epigenetic mechanisms in cancer are discussed, with a focus on potential diagnostic epigenetic biomarkers in ovarian cancer in tissue and body fluids. A literature search was undertaken (on 22-09-2011) for these subjects using the search syntax (((((((((((((((“ovarian”) OR “ovary”) OR “ovarian cancer”) OR “ovarian cancers”) OR “cancer of the ovary”) OR “tumour of the ovary”) OR “ovarian tumor”) OR “ovarian tumors”) OR “ovarian tumour”) OR “ovarian tumours”) OR “ovarian neoplasm”) OR “ovarian neoplasms” OR “ovarian carcinoma”) OR “ovarian carcinomas”) OR “carcinoma of the ovary”)) AND (((((((((“epigenetics”) OR “epigenetic”) OR “epigenome”) OR “methylation”) OR “hypermethylation”) OR “chromatin modification”) OR “histone”) OR “histones”) OR “acetylation”)

Expert opinion: To date no single epigenetic biomarker is able to accurately detect early ovarian cancer in either tissue or body fluids. A panel of epigenetic biomarkers based on aberrant DNA methylation in body fluids, especially blood, has the best chance of being implemented in clinical practice, as it is semi-invasive. However, progression toward clinical use is hampered by the lack of detection techniques combining high throughput and accuracy with low cost, by difficulties in establishing reliable reference values and by the heterogeneous nature of ovarian cancer. Until addressed, implementation as a diagnostic measure complimenting current techniques in select cases seems a far way to go, and implementation as a primary screening tool is yet even farther away.

Declaration of interest

This work was supported by ‘De Hendrik Muller Stichting', ‘Het Vreedefonds', ‘Stichting de Fundatie van de Vrijvrouwe van Renswoude' and ‘Studiefonds Ketel 1'.

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