dc.contributor.author
Psilopatis, Iason
dc.contributor.author
Vrettou, Kleio
dc.contributor.author
Fleckenstein, Florian Nima
dc.contributor.author
Theocharis, Stamatios
dc.date.accessioned
2024-04-08T13:44:48Z
dc.date.available
2024-04-08T13:44:48Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/42983
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-42697
dc.description.abstract
Endometriosis is a chronic disorder of the female reproductive system which afflicts a great number of women worldwide. Histone deacetylases (HDACs) prevent the relaxation of chromatin, thereby positively or negatively modulating gene transcription. The current review aims at studying the impact of histone modifications and their therapeutic targeting in endometriosis. In order to identify relevant studies, a literature review was conducted using the MEDLINE and LIVIVO databases. The current manuscript represents the most comprehensive, up-to-date review of the literature focusing on the particular role of HDACs and their inhibitors in the context of endometriosis. HDAC1, HDAC2, HDAC3, Sirtuin 1, and Sirtuin 3, are the five most studied HDAC enzymes which seem to, at least partly, influence the pathophysiology of endometriosis. Both well-established and novel HDACIs could possibly represent modern, efficacious anti-endometriotic drug agents. Altogether, histone modifications and their therapeutic targeting have been proven to have a strong impact on endometriosis.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
endometriosis
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
The Impact of Histone Modifications in Endometriosis Highlights New Therapeutic Opportunities
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
1227
dcterms.bibliographicCitation.doi
10.3390/cells12091227
dcterms.bibliographicCitation.journaltitle
Cells
dcterms.bibliographicCitation.number
9
dcterms.bibliographicCitation.originalpublishername
MDPI AG
dcterms.bibliographicCitation.volume
12
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
37174627
dcterms.isPartOf.eissn
2073-4409