Publication:
Enhanced inflammatory activity of endometriotic lesions from the rectovaginal septum.

cris.virtual.author-orcid0000-0002-9881-1252
cris.virtualsource.author-orcid8f0fb243-dbd0-4db2-91d6-32503b556a93
cris.virtualsource.author-orcid45405e65-2f71-4024-b909-c41ee2ff6a10
cris.virtualsource.author-orcid0372c0db-cd19-4800-828f-edddddb37f44
cris.virtualsource.author-orcid739973bf-27d2-4e55-932c-d9b5649868a0
datacite.rightsopen.access
dc.contributor.authorBertschi, Dominic
dc.contributor.authorMc Kinnon, Brett
dc.contributor.authorEvers, Jakob
dc.contributor.authorBersinger, Nick A.
dc.contributor.authorMueller, Michael
dc.date.accessioned2024-10-15T14:10:17Z
dc.date.available2024-10-15T14:10:17Z
dc.date.issued2013
dc.description.abstractEndometriosis is characterised by the growth of ectopic lesions at multiple locations outside the uterine cavity and may be considered a collection of distinct but related conditions. The exact aetiology of endometriosis is still not clear although a role for inflammation is increasingly accepted. We therefore investigated the inflammatory activity of eutopic tissue and that of the matching ectopic lesions from different locations by measuring the genetic expression of inflammatory chemokines and cytokines. The gene expression in matching eutopic and ectopic tissue was compared, as was the gene expression in lesions from different locations. A significantly higher mRNA expression of the chemokines ENA-78 and RANTES and the cytokines IL-6 and TNF α was observed in endometriotic lesions of the rectovaginal septum (RVS) compared to that of matching eutopic tissue. Comparisons across lesion locations showed a significantly higher expression of IL-6 and TNF α in the RVS compared to lesions from either the ovaries or the peritoneum. These results show that the production of some inflammatory chemokines and cytokines is significantly increased in the ectopic endometrial tissue compared to matching eutopic tissue. Furthermore, IL-6 and TNF α are produced in significantly higher quantities in RVS lesions compared to other lesions.
dc.description.sponsorshipUniversitätsklinik für Frauenheilkunde
dc.description.sponsorshipDepartement Klinische Forschung, Forschungsgruppe Endometriose und gynäkologische Onkologie
dc.identifier.doi10.7892/boris.54055
dc.identifier.pmid24453419
dc.identifier.publisherDOI10.1155/2013/450950
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/124456
dc.language.isoen
dc.publisherHindawi Publishing Corp.
dc.relation.ispartofMediators of inflammation
dc.relation.issn0962-9351
dc.relation.organizationDCD5A442C056E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C067E17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleEnhanced inflammatory activity of endometriotic lesions from the rectovaginal septum.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue450950
oaire.citation.startPage450950
oaire.citation.volume2013
oairecerif.author.affiliationDepartement Klinische Forschung, Forschungsgruppe Endometriose und gynäkologische Onkologie
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliationUniversitätsklinik für Frauenheilkunde
oairecerif.author.affiliation2Universitätsklinik für Frauenheilkunde
oairecerif.author.affiliation2Departement Klinische Forschung, Forschungsgruppe Endometriose und gynäkologische Onkologie
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unibe.description.ispublishedpub
unibe.eprints.legacyId54055
unibe.journal.abbrevTitleMEDIAT INFLAMM
unibe.refereedtrue
unibe.subtype.articlejournal

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