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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 |
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dc.contributor.author | Lee, SH | - |
dc.contributor.author | Lim, SY | - |
dc.contributor.author | Choi, JH | - |
dc.contributor.author | Jung, JC | - |
dc.contributor.author | Oh, S | - |
dc.contributor.author | Kook, KH | - |
dc.contributor.author | Choi, YH | - |
dc.date.accessioned | 2016-11-09T01:26:09Z | - |
dc.date.available | 2016-11-09T01:26:09Z | - |
dc.date.issued | 2014 | - |
dc.identifier.issn | 1226-3613 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/12799 | - |
dc.description.abstract | The 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.iso | en | - |
dc.subject.MESH | Cells, Cultured | - |
dc.subject.MESH | Chalcone | - |
dc.subject.MESH | Diarylheptanoids | - |
dc.subject.MESH | Fibroblasts | - |
dc.subject.MESH | Graves Ophthalmopathy | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Interferon-gamma | - |
dc.subject.MESH | Orbit | - |
dc.subject.MESH | RNA, Messenger | - |
dc.subject.MESH | STAT1 Transcription Factor | - |
dc.title | Benzylideneacetophenone derivatives attenuate IFN-γ-induced IP-10/CXCL10 production in orbital fibroblasts of patients with thyroid-associated ophthalmopathy through STAT-1 inhibition. | - |
dc.type | Article | - |
dc.identifier.pmid | 24924312 | - |
dc.identifier.url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4081550/ | - |
dc.contributor.affiliatedAuthor | 국, 경훈 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1038/emm.2014.26 | - |
dc.citation.title | Experimental & molecular medicine | - |
dc.citation.volume | 46 | - |
dc.citation.date | 2014 | - |
dc.citation.startPage | e100 | - |
dc.citation.endPage | e100 | - |
dc.identifier.bibliographicCitation | Experimental & molecular medicine, 46. : e100-e100, 2014 | - |
dc.identifier.eissn | 2092-6413 | - |
dc.relation.journalid | J012263613 | - |
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