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  1. H-2. ナノ生命科学研究所
  2. h-2 10.学術雑誌掲載論文
  3. 1. 査読済論文

Regulation of Cytochrome b5 Expression by miR-223 in Human Liver: Effects on Cytochrome P450 Activities

https://doi.org/10.24517/00015109
https://doi.org/10.24517/00015109
2ba6c103-87b7-41db-9437-fc972e7623cc
名前 / ファイル ライセンス アクション
PH-PR-NAKAJIMA-M-780.pdf PH-PR-NAKAJIMA-M-780.pdf (617.5 kB)
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Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-04
タイトル
タイトル Regulation of Cytochrome b5 Expression by miR-223 in Human Liver: Effects on Cytochrome P450 Activities
言語
言語 eng
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
ID登録
ID登録 10.24517/00015109
ID登録タイプ JaLC
著者 Takahashi, Kei

× Takahashi, Kei

WEKO 27286

Takahashi, Kei

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Oda, Yuki

× Oda, Yuki

WEKO 27287

Oda, Yuki

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Toyoda, Yasuyuki

× Toyoda, Yasuyuki

WEKO 27288

Toyoda, Yasuyuki

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Fukami, Tatsuki

× Fukami, Tatsuki

WEKO 26716
e-Rad 00532300
金沢大学研究者情報 00532300
研究者番号 00532300

Fukami, Tatsuki

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Yokoi, Tsuyoshi

× Yokoi, Tsuyoshi

WEKO 63
研究者番号 70135226

Yokoi, Tsuyoshi

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Nakajima, Miki

× Nakajima, Miki

WEKO 196
e-Rad 70266162
金沢大学研究者情報 70266162
研究者番号 70266162

Nakajima, Miki

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著者別表示 深見, 達基

× 深見, 達基

深見, 達基

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横井, 毅

× 横井, 毅

横井, 毅

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中嶋, 美紀

× 中嶋, 美紀

中嶋, 美紀

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提供者所属
内容記述タイプ Other
内容記述 金沢大学ナノ生命科学研究所 / 金沢大学医薬保健研究域薬学系
書誌情報 Pharmaceutical Research

巻 31, 号 3, p. 780-794, 発行日 2014-03-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0724-8741
NCID
収録物識別子タイプ NCID
収録物識別子 AA10632083
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1007/s11095-013-1200-7
出版者
出版者 Springer
抄録
内容記述タイプ Abstract
内容記述 Purpose: Cytochrome b 5 (b 5) is a hemoprotein that transfers electrons to several enzymes to fulfill functions in fatty acid desaturation, methemoglobin reduction, steroidogenesis, and drug metabolism. Despite the importance of b 5, the regulation of b 5 expression in human liver remains largely unknown. We investigated whether microRNA (miRNA) might be involved in the regulation of human b 5. Methods: Twenty-four human liver specimens were used for correlation analysis. In silico analysis and luciferase assay were performed to determine whether the predicted miRNAs functionally target to b 5. The miR-223 was overexpressed into HepG2 cells infected with adenovirus expressing human cytochrome P450. Results: In human livers, the b 5 protein levels were not positively correlated with the b 5 mRNA levels, and miR-223 levels were inversely correlated with the b 5 mRNA levels or the translational efficiencies. The luciferase assay showed that miR-223 functionally binds to the element in the 3′-untranslated region of b 5 mRNA. The overexpression of miR-223 significantly reduced the endogenous b 5 protein level and the mRNA stability in HepG2 cells. Moreover, the overexpression of miR-223 significantly reduced CYP3A4-catalyzed testosterone 6β-hydroxylation activity and CYP2E1-catalyzed chlorzoxazone 6-hydroxylase activity but not CYP1A2-catalyzed 7-ethoxyresorufin O-deethylase activity. Conclusions: miR-223 down-regulates b 5 expression in the human liver, modulating P450 activities. © 2013 Springer Science+Business Media New York.
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
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