Eldecalcitol (ED-71)-induced exosomal miR-6887-5p suppresses squamous cell carcinoma cell growth by targeting heparin-binding protein 17/fibroblast growth factor–binding protein-1 (HBp17/FGFBP-1)
In Vitro Cellular and Developmental Biology - Animal 56 巻 3 号
222-233 頁
2020-03-17 発行
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InVitroCellDevBiolAnim_56_222.pdf
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タイトル ( eng ) |
Eldecalcitol (ED-71)-induced exosomal miR-6887-5p suppresses squamous cell carcinoma cell growth by targeting heparin-binding protein 17/fibroblast growth factor–binding protein-1 (HBp17/FGFBP-1)
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作成者 |
Higaki M.
Rosli S. N. Z.
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収録物名 |
In Vitro Cellular and Developmental Biology - Animal
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巻 | 56 |
号 | 3 |
開始ページ | 222 |
終了ページ | 233 |
抄録 |
Heparin-binding protein 17/fibroblast growth factor–binding protein-1 (HBp17/FGFBP-1) was purified from A431 cell-conditioned media based on its capacity to bind to fibroblast growth factor 1 and 2 (FGF-1 and FGF-2). HBp17/FGFBP-1 has been observed to induce the tumorigenic potential of epithelial cells and is highly expressed in oral cancer cell lines and tissues. HBp17/FGFBP-1 is also recognized as a pro-angiogenic molecule as a consequence of its interaction with FGF-2. We have previously reported that Eldecalcitol (ED-71), an analog of 1α,25(OH)2D3, downregulated the expression of HBp17/FGFBP-1 and inhibited the proliferation of squamous cell carcinoma (SCC) cells in vitro and in vivo through NF-κb inhibition. To explore the possibility of microRNA (miRNA) control of HBp17/FGFBP-1, we analyzed exosomal miRNAs from medium conditioned by A431 cells treated with ED-71. Microarray analysis revealed that 12 exosomal miRNAs were upregulated in ED-71-treated A431 cells. Among them, miR-6887-5p was identified to have a predicted mRNA target matching the 3′ untranslated region (3′-UTR) of HBp17/FGFBP-1. The 3′-UTR of HBp17/FGFBP-1 was confirmed to be a direct target of miR-6887-5p in SCC/OSCC cells, as assessed with a luciferase reporter assay. Functional assessment revealed that overexpression of miR-6887-5p in SCC/OSCC cells inhibited cell proliferation and colony formation in vitro, and inhibited tumor growth in vivo compared with control. In conclusion, our present study supports a novel anti-cancer mechanism involving the regulation of HBp17/FGFBP-1 function by exosomal miR-6887-5p in SCC/OSCC cells, which has potential utility as a miRNA-based cancer therapy.
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著者キーワード |
miR-6887-5p
Eldecalcitol (ED-71)
HBp17/FGFBP-1
Oral squamous cell carcinoma
Exosome
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内容記述 |
This research was supported in part by Grants-in-Aid for Scientific Research from the Japanese Ministry of Education, Culture, Sports, Science and Technology to T.O. (grant number: 15H05043) and T. S. (grant number: 16K11723).
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言語 |
英語
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資源タイプ | 学術雑誌論文 |
出版者 |
The Society for In Vitro Biology
Springer Verlag
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発行日 | 2020-03-17 |
権利情報 |
This is a post-peer-review, pre-copyedit version of an article published in In Vitro Cellular and Developmental Biology - Animal. The final authenticated version is available online at: https://doi.org/10.1007/s11626-020-00440-x
This is not the published version. Please cite only the published version. この論文は出版社版ではありません。引用の際には出版社版をご確認、ご利用ください。
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出版タイプ | Author’s Original(十分な品質であるとして、著者から正式な査読に提出される版) |
アクセス権 | オープンアクセス |
収録物識別子 |
[ISSN] 1071-2690
[ISSN] 1543-706X
[DOI] 10.1007/s11626-020-00440-x
[PMID] 32185608
[DOI] https://doi.org/10.1007/s11626-020-00440-x
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