ID | 115041 |
タイトル別表記 | RANKLが誘導する破骨細胞分化におけるROSの役割と、Febuxostatによる破骨細胞分化抑制効果
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著者 |
アシテル, モハナッド
徳島大学大学院口腔科学教育部(口腔科学専攻)
Bat-Erdene, Ariunzaya
Mongolian National University of Medical Sciences
Oda, Asuka
Tokushima University
谷本, 幸多朗
Tokushima University
Higa, Yoshiki
Tokushima University
Udaka, Kengo
Tokushima University
Takahashi, Mamiko
Tokushima University
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キーワード | RANKL
ROS
doxorubicin
multiple myeloma
osteoclastogenesis
ovariectomy
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資料タイプ |
学位論文
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抄録 | Receptor activator of NF-κB ligand (RANKL), a critical mediator of osteoclastogenesis, is upregulated in multiple myeloma (MM). The xanthine oxidase inhibitor febuxostat, clinically used for prevention of tumor lysis syndrome, has been demonstrated to effectively inhibit not only the generation of uric acid but also the formation of reactive oxygen species (ROS). ROS has been demonstrated to mediate RANKL-mediated osteoclastogenesis. In the present study, we therefore explored the role of cancer-treatment-induced ROS in RANKL-mediated osteoclastogenesis and the suppressive effects of febuxostat on ROS generation and osteoclastogenesis. RANKL dose-dependently induced ROS production in RAW264.7 preosteoclastic cells; however, febuxostat inhibited the RANKL-induced ROS production and osteoclast (OC) formation. Interestingly, doxorubicin (Dox) further enhanced RANKL-induced osteoclastogenesis through upregulation of ROS production, which was mostly abolished by addition of febuxostat. Febuxostat also inhibited osteoclastogenesis enhanced in cocultures of bone marrow cells with MM cells. Importantly, febuxostat rather suppressed MM cell viability and did not compromise Dox’s anti-MM activity. In addition, febuxostat was able to alleviate pathological osteoclastic activity and bone loss in ovariectomized mice. Collectively, these results suggest that excessive ROS production by aberrant RANKL overexpression and/or anticancer treatment disadvantageously impacts bone, and that febuxostat can prevent the ROS-mediated osteoclastic bone damage.
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掲載誌名 |
Cancers
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ISSN | 20726694
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出版者 | MDPI
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巻 | 12
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号 | 4
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開始ページ | 929
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発行日 | 2020-04-09
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備考 | 内容要旨・審査要旨・論文本文の公開
本論文は,著者Mohannad Ashtarの学位論文として提出され,学位審査・授与の対象となっている。 |
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/).
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EDB ID | |
出版社版DOI | |
出版社版URL | |
フルテキストファイル | |
言語 |
eng
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著者版フラグ |
博士論文全文を含む
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文科省報告番号 | 甲第3467号
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学位記番号 | 甲口第466号
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学位授与年月日 | 2020-12-10
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学位名 |
博士(歯学)
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学位授与機関 |
徳島大学
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部局 |
歯学系
病院
医学系
先端酵素学研究所
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