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TIS21(/BTG2/PC3) inhibits interleukin-6 expression via downregulation of STAT3 pathway.

DC Field Value Language
dc.contributor.authorQuy, LN-
dc.contributor.authorChoi, YW-
dc.contributor.authorKim, YH-
dc.contributor.authorChwae, YJ-
dc.contributor.authorPark, TJ-
dc.contributor.authorLim, IK-
dc.date.accessioned2014-04-30-
dc.date.available2014-04-30-
dc.date.issued2013-
dc.identifier.issn0898-6568-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/9868-
dc.description.abstractCancer cell growth was increased when co-cultured with fibroblasts, however, no effect was observed when co-cultured with TIS21-overexpressed fibroblast. Therefore, the role of TIS21 played in cancer microenvironment was investigated. TIS21 decreased interleukin-6 (IL-6) expression in human dermal fibroblast (HDF). Adenoviral transduction of TIS21 gene to HDF decreased the secretion of IL-6, whereas knockdown of the gene increased IL-6 expression. Furthermore, TIS21 overexpression inhibited STAT3 binding to IL-6 promoter region as well as JAK2-STAT3 signaling by inhibiting reactive oxygen species (ROS) generation by being localized in mitochondria. Mitochondria-target TIS21 (MT-TIS21) also inhibited IL-6 expression by downregulating STAT3 phosphorylation, whereas NF-κB pathway was not influenced by TIS21 expression. These results indicate that TIS21 negatively regulated cancer cell growth by inhibiting IL-6 expression through downregulation of STAT3 activation.-
dc.language.isoen-
dc.titleTIS21(/BTG2/PC3) inhibits interleukin-6 expression via downregulation of STAT3 pathway.-
dc.typeArticle-
dc.identifier.pmid23917204-
dc.identifier.urlhttp://linkinghub.elsevier.com/retrieve/pii/S0898-6568(13)00222-2-
dc.subject.keywordInterleukin-6-
dc.subject.keywordJAK2-
dc.subject.keywordROS-
dc.subject.keywordSTAT3-
dc.subject.keywordTIS21(/BTG2/PC3)-
dc.contributor.affiliatedAuthor최, 용준-
dc.contributor.affiliatedAuthor박, 태준-
dc.contributor.affiliatedAuthor임, 인경-
dc.type.localJournal Papers-
dc.identifier.doi10.1016/j.cellsig.2013.07.024-
dc.citation.titleCellular signalling-
dc.citation.volume25-
dc.citation.number12-
dc.citation.date2013-
dc.citation.startPage2391-
dc.citation.endPage2399-
dc.identifier.bibliographicCitationCellular signalling, 25(12). : 2391-2399, 2013-
dc.identifier.eissn1873-3913-
dc.relation.journalidJ008986568-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Microbiology
Journal Papers > School of Medicine / Graduate School of Medicine > Biochemistry & Molecular Biology
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