Cited 0 times in Scipus Cited Count

Benzylideneacetophenone derivatives attenuate IFN-γ-induced IP-10/CXCL10 production in orbital fibroblasts of patients with thyroid-associated ophthalmopathy through STAT-1 inhibition.

DC Field Value Language
dc.contributor.authorLee, SH-
dc.contributor.authorLim, SY-
dc.contributor.authorChoi, JH-
dc.contributor.authorJung, JC-
dc.contributor.authorOh, S-
dc.contributor.authorKook, KH-
dc.contributor.authorChoi, YH-
dc.date.accessioned2016-11-09T01:26:09Z-
dc.date.available2016-11-09T01:26:09Z-
dc.date.issued2014-
dc.identifier.issn1226-3613-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/12799-
dc.description.abstractThe aim of the present study was to identify a new candidate anti-inflammatory

compound for use in the active stage of thyroid-associated ophthalmopathy (TAO).

Benzylideneacetophenone compound JC3

[(2E)-3-(4-hydroxy-3-methoxyphenyl)phenylpro-2-en-l-one] was synthesized based on

a structural modification of yakuchinone B, a constituent of the seeds of Alpinia

oxyphylla, which belongs to the ginger family (Zingiberaceae), has been widely

used in folk medicine as an anti-inflammatory phytochemical. Orbital fibroblasts

were primarily cultured from patients with TAO, and the potential of JC3 to

suppress the interferon (IFN)-gamma-induced protein (IP)-10/CXCL10 production in

these cells was determined. IFN-gamma strongly increased the level of

IP-10/CXCL10 in orbital fibroblasts from patients with TAO. JC3 exerted a

significant inhibitory effect on the IFN-gamma-induced increase in IP-10/CXCL10

in a dose-dependent manner; its potency was greater than that of an identical

concentration of yakuchinone B with no toxicity to cells at the concentration

range used. Moreover, the constructed dimer and trimer polystructures of JC3,

showed greater potency than JC3 in suppressing the IFN-gamma-induced production

of IP-10/CXCL10. JC3 significantly attenuated the IP-10/CXCL10 mRNA expression

induced by IFN-gamma, and a gel-shift assay showed that JC3 suppressed

IFN-gamma-induced DNA binding of signal transducer and activator of

transcription-1 (STAT-1) in TAO orbital fibroblasts. Our results provide initial

evidence that the JC3 compound reduces the levels of IP-10/CXCL10 protein and

mRNA induced by IFN-gamma in orbital fibroblasts of TAO patients. Therefore, JC3

might be considered as a future candidate for therapeutic application in TAO that

exerts its effects by modulating the pathogenic mechanisms in orbital

fibroblasts.
-
dc.language.isoen-
dc.subject.MESHCells, Cultured-
dc.subject.MESHChalcone-
dc.subject.MESHDiarylheptanoids-
dc.subject.MESHFibroblasts-
dc.subject.MESHGraves Ophthalmopathy-
dc.subject.MESHHumans-
dc.subject.MESHInterferon-gamma-
dc.subject.MESHOrbit-
dc.subject.MESHRNA, Messenger-
dc.subject.MESHSTAT1 Transcription Factor-
dc.titleBenzylideneacetophenone derivatives attenuate IFN-γ-induced IP-10/CXCL10 production in orbital fibroblasts of patients with thyroid-associated ophthalmopathy through STAT-1 inhibition.-
dc.typeArticle-
dc.identifier.pmid24924312-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081550/-
dc.contributor.affiliatedAuthor국, 경훈-
dc.type.localJournal Papers-
dc.identifier.doi10.1038/emm.2014.26-
dc.citation.titleExperimental & molecular medicine-
dc.citation.volume46-
dc.citation.date2014-
dc.citation.startPagee100-
dc.citation.endPagee100-
dc.identifier.bibliographicCitationExperimental & molecular medicine, 46. : e100-e100, 2014-
dc.identifier.eissn2092-6413-
dc.relation.journalidJ012263613-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Ophthalmology
Files in This Item:
24924312.pdfDownload

qrcode

해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse