Abemaciclib-induced epithelial-mesenchymal transition mediated by cyclin-dependent kinase 4/6 independent of cell cycle arrest pathway
The International Journal of Biochemistry & Cell Biology 172 巻
106601- 頁
2024-05-29 発行
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この文献の参照には次のURLをご利用ください : https://ir.lib.hiroshima-u.ac.jp/00055842
ファイル情報(添付) |
利用開始日
2025-05-29
1.02 MB
種類 :
全文
エンバーゴ :
2025-05-29
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タイトル ( eng ) |
Abemaciclib-induced epithelial-mesenchymal transition mediated by cyclin-dependent kinase 4/6 independent of cell cycle arrest pathway
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作成者 |
Yoshimori Tomoyo
Kumagai Yuta
Futatsugi Sorahito
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収録物名 |
The International Journal of Biochemistry & Cell Biology
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巻 | 172 |
開始ページ | 106601 |
抄録 |
Abemaciclib (ABM), a cyclin-dependent kinase 4/6 inhibitor, shows pharmacological effects in cell cycle arrest. Epithelial-mesenchymal transition is an important cellular event associated with pathophysiological states such as organ fibrosis and cancer progression. In the present study, we evaluated the contribution of factors associated with cell cycle arrest to ABM-induced epithelial-mesenchymal transition. Treatment with 0.6 µM ABM induced both cell cycle arrest and epithelial-mesenchymal transition-related phenotypic changes. Interestingly, the knockdown of cyclin-dependent kinase 4/6, pharmacological targets of ABM or cyclin D1, which forms complexes with cyclin-dependent kinase 4/6, resulted in cell cycle arrest at the G1-phase and induction of epithelial-mesenchymal transition, indicating that downregulation of cyclin-dependent kinase 4/6-cyclin D1 complexes would mimic ABM. In contrast, knockdown of the Rb protein, which is phosphorylated by cyclin-dependent kinase 4/6, had no effect on the expression level of α-smooth muscle actin, an epithelial-mesenchymal transition marker. Furthermore, ABM-induced epithelial-mesenchymal transition was not affected by Rb knockdown, suggesting that Rb is not involved in the transition process. Our study is the first to suggest that cyclin-dependent kinase 4/6-cyclin D1 complexes, as pharmacological targets of ABM, may contribute to ABM-induced epithelial-mesenchymal transition, followed by clinical disorders such as organ fibrosis and cancer progression. This study suggests that blocking epithelial-mesenchymal transition might be a promising way to prevent negative side effects caused by a medication (ABM) without affecting its ability to treat the disease.
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著者キーワード |
abemaciclib
Cell Cycle arrest
Cyclin D1
Cyclin-dependent kinase 4/6
Epithelial-mesenchymal transition
Rb protein
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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 |
Elsevier
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発行日 | 2024-05-29 |
権利情報 |
© 2024. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/
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 | Accepted Manuscript(出版雑誌の一論文として受付されたもの。内容とレイアウトは出版社の投稿様式に沿ったもの) |
アクセス権 | エンバーゴ期間中 |
収録物識別子 |
[DOI] https://doi.org/10.1016/j.biocel.2024.106601
~の異版である
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助成機関名 |
日本学術振興会
Japan Society for the Promotion of Science
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助成機関識別子 |
[Crossref Funder] https://doi.org/10.13039/501100001691
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研究課題名 |
肺胞上皮細胞におけるPEPT2介在性輸送および自然免疫応答に及ぼす薬物の影響
肺胞上皮細胞におけるPEPT2介在性輸送および自然免疫応答に及ぼす薬物の影響
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研究課題番号 |
21K06668
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助成機関名 |
日本学術振興会
Japan Society for the Promotion of Science
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助成機関識別子 |
[Crossref Funder] https://doi.org/10.13039/501100001691
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研究課題名 |
抗がん効果と上皮間葉転換の比較を基軸としたがん悪性化機構の解明とその応用展開
Mechanistic study on cancer progression based on the comparison between antitumor effects and epithelial-mesenchymal transition by anticancer drugs
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研究課題番号 |
22K06766
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助成機関名 |
日本学術振興会
Japan Society for the Promotion of Science
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助成機関識別子 |
[Crossref Funder] https://doi.org/10.13039/501100001691
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研究課題名 |
肺胞マクロファージの自然免疫応答と肺胞上皮細胞の上皮間葉転換との連関解析
Analysis of innate immune response of alveolar macrophages and epithelial-mesenchymal transition of alveolar epithelial cells
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研究課題番号 |
22K06698
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備考 | The full-text file will be made open to the public on 29 May 2025 in accordance with publisher's 'Terms and Conditions for Self-Archiving' |