このエントリーをはてなブックマークに追加
ID 70250
フルテキストURL
fulltext.pdf 3.31 MB
著者
Furutani, Yuji Faculty of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Shimasaki, Natsuki Faculty of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Yamada, Riko Faculty of Interdisciplinary Science and Engineering in Health Systems, Okayama University
Ohtsuki, Takashi Faculty of Interdisciplinary Science and Engineering in Health Systems, Okayama University ORCID Kaken ID publons researchmap
Watanabe, Kazunori Faculty of Interdisciplinary Science and Engineering in Health Systems, Okayama University ORCID Kaken ID publons researchmap
抄録
Hyperthermia is a minimally invasive cancer treatment based on heat stress-induced apoptosis. Its therapeutic efficacy, however, is often limited by tumor heterogeneity and acquired thermotolerance. Therefore, combination strategies involving hyperthermia and chemotherapy have been developed to enhance the therapeutic efficacy. Previously, we showed that SB366791 enhanced heat-induced apoptosis by inhibiting heat stress-induced scaffold attachment factor B (SAFB) granule formation, although its proapoptotic activity was insufficient. Therefore, we screened to identify novel compounds that enhance heat-induced apoptosis by suppressing SAFB granule formation. We identified four hit compounds that inhibited SAFB granule formation, all exhibiting thermal enhancement ratios > 1.0─that significantly enhanced heat-induced apoptosis efficiency. Additionally, the tumor volume in mice treated with a combination of Z19024498 and hyperthermia was significantly smaller than that in mice treated with hyperthermia or Z19024498. These results indicate that the identified compounds, specifically Z19024498, have potential as thermal sensitizers for hyperthermia therapy.
発行日
2026-02-18
出版物タイトル
Journal of Medicinal Chemistry
69巻
5号
出版者
American Chemical Society (ACS)
開始ページ
5944
終了ページ
5955
ISSN
0022-2623
NCID
AA00702411
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2026 The Authors.
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1021/acs.jmedchem.5c03361
ライセンス
https://creativecommons.org/licenses/by-nc-nd/4.0/
助成情報
( 公益財団法人ウエスコ学術振興財団 / Wesco Scientific Promotion Foundation )
( 公益財団法人天野工業技術研究所 / Amano Institute of Technology )
21am0101084: 創薬基盤の融合による戦略的イノベーション創出(化合物ライブラリー整備と支援・高度化による創薬研究の推進) ( 国立研究開発法人日本医療研究開発機構 / Japan Agency for Medical Research and Development )