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  1. 115 原爆後障害医療研究所 = Atomic Bomb Disease Institute
  2. 115 学術雑誌論文 = Articles in academic journal

DHMEQ, a novel NF-kappaB inhibitor, suppresses growth and type I collagen accumulation in keloid fibroblasts

http://hdl.handle.net/10069/16875
http://hdl.handle.net/10069/16875
296b8b7a-6d48-4cb7-a4d1-a4c076745807
名前 / ファイル ライセンス アクション
JDS51_171.pdf JDS51_171.pdf (447.3 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2008-05-07
タイトル
タイトル DHMEQ, a novel NF-kappaB inhibitor, suppresses growth and type I collagen accumulation in keloid fibroblasts
言語
言語 eng
キーワード
主題Scheme Other
主題 Keloid
キーワード
主題Scheme Other
主題 NF-kappaB
キーワード
主題Scheme Other
主題 DHMEQ
キーワード
主題Scheme Other
主題 Type I collagen
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Makino, Sachio

× Makino, Sachio

Makino, Sachio

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Mitsutake, Norisato

× Mitsutake, Norisato

Mitsutake, Norisato

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Nakashima, Masahiro

× Nakashima, Masahiro

Nakashima, Masahiro

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A., Saenko Vladimir

× A., Saenko Vladimir

A., Saenko Vladimir

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Ohtsuru, Akira

× Ohtsuru, Akira

Ohtsuru, Akira

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Umezawa, Kazuo

× Umezawa, Kazuo

Umezawa, Kazuo

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Tanaka, Katsumi

× Tanaka, Katsumi

Tanaka, Katsumi

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Hirano, Akiyoshi

× Hirano, Akiyoshi

Hirano, Akiyoshi

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Yamashita, Shunichi

× Yamashita, Shunichi

Yamashita, Shunichi

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抄録
内容記述タイプ Abstract
内容記述 Background:Keloid is a benign dermal tumor characterized by proliferation of dermal fibroblasts and overproduction of extracellular matrix (ECM). Nuclear factor kappaB (NF-κB) plays an important role in regulation of inflammation, immune response and cell proliferation. Activation of the NF-κB pathway is thought to be closely linked to abnormal cell proliferation and ECM production in keloid fibroblasts. Objective:This study was set out to investigate the effects of a novel selective NF-κB inhibitor, dehydroxymethylepoxyquinomicin (DHMEQ), on keloid fibroblasts. Methods:Primary normal and keloid dermal fibroblasts were used for this study. NF-κB activity was assessed by DNA-binding assay and immunohistochemistry. The effect of DHMEQ was evaluated by cell viability, cell growth and type I collagen accumulation. Results:Basal NF-κB activity was constitutively elevated in keloid fibroblasts, indicating that this pathway is involved in keloid pathogenesis. DHMEQ markedly reduced cell proliferation and type I collagen accumulation in keloid fibroblasts. Conclusion:The inhibition of NF-κB by DHMEQ may be an attractive therapeutic approach for keloids.
書誌情報 号 3, p. 171-180, 発行日 2008-09
ISSN
収録物識別子タイプ ISSN
収録物識別子 09231811
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AA11531842
PubMed番号
関連タイプ isVersionOf
識別子タイプ PMID
関連識別子 18406579
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1016/j.jdermsci.2008.03.003
権利
権利情報 Copyright (c) 2008 Japanese Society for Investigative Dermatology Published by Elsevier Ireland Ltd.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
引用
内容記述タイプ Other
内容記述 Journal of Dermatological Science, 51(3), pp.171-180; 2008
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