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The MicroRNA-23b/27b/24 Cluster Facilitates Colon Cancer Cell Migration by Targeting FOXP2

https://tokushima-u.repo.nii.ac.jp/records/2007104
https://tokushima-u.repo.nii.ac.jp/records/2007104
edb87e57-aa0d-4df6-bccd-6e1226a24d3f
名前 / ファイル ライセンス アクション
cancers_12_1_174.pdf cancers_12_1_174.pdf (2.52 MB)
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アイテムタイプ 文献 / Documents(1)
公開日 2020-02-04
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
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
出版社版DOI
関連識別子 https://doi.org/10.3390/cancers12010174
関連名称 10.3390/cancers12010174
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
タイトル
タイトル The MicroRNA-23b/27b/24 Cluster Facilitates Colon Cancer Cell Migration by Targeting FOXP2
著者 西田, 憲生

× 西田, 憲生

WEKO 546
徳島大学 教育研究者総覧 241627/profile-ja.html
e-Rad_Researcher 10624033

ja 西田, 憲生

ja-Kana ニシダ, ケンセイ

en Nishida, Kensei

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桑野, 由紀

× 桑野, 由紀

WEKO 392
徳島大学 教育研究者総覧 193042/profile-ja.html
e-Rad_Researcher 00563454

ja 桑野, 由紀

ja-Kana クワノ, ユキ

en Kuwano, Yuki

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六反, 一仁

× 六反, 一仁

WEKO 1581
徳島大学 教育研究者総覧 60135/profile-ja.html
e-Rad_Researcher 10230898

ja 六反, 一仁

ja-Kana ロクタン, カズヒト

en Rokutan, Kazuhito

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抄録
内容記述 Acquisition of cell migration capacity is an early and essential process in cancer development. The aim of this study was to identify microRNA gene expression networks that induced high migration capacity. Using colon cancer HCT116 cells subcloned by transwell-based migrated cell selection, microRNA array analysis was performed to examine the microRNA expression profile. Promoter activity and microRNA targets were assessed with luciferase reporters. Cell migration capacity was assessed by either the transwell or scratch assay. In isolated subpopulations with high migration capacity, the expression levels of the miR-23b/27b/24 cluster increased in accordance with the increased expression of the short C9orf3 transcript, a host gene of the miR-23b/27b/24 cluster. E2F1-binding sequences were involved in the basic transcription activity of the short C9orf3 expression, and E2F1-small-interfering (si)RNA treatment reduced the expression of both the C9orf3 and miR-23b/27b/24 clusters. Overexpression experiments showed that miR-23b and miR-27b promoted cell migration, but the opposite effect was observed with miR-24. Forkhead box P2 (FOXP2) mRNA and protein levels were reduced by both/either miR-23b and miR-27b. Furthermore, FOXP2 siRNA treatment significantly promoted cell migration. Our findings demonstrated a novel role of the miR-23b/27b/24 cluster in cell migration through targeting FOXP2, with potential implications for the development of microRNA-based therapy targeted at inhibiting cancer migration.
キーワード
主題 cell migration
キーワード
主題 miR-23b/27b/24 cluster
キーワード
主題 C9orf3
キーワード
主題 FOXP2
書誌情報 en : Cancers

巻 12, 号 1, p. 174, 発行日 2020-01-10
収録物ID
収録物識別子タイプ ISSN
収録物識別子 20726694
出版者
出版者 MDPI
権利情報
権利情報 © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
EID
識別子 362698
言語
言語 eng
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