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ID 70250
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Author
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
Abstract
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.
Published Date
2026-02-18
Publication Title
Journal of Medicinal Chemistry
Volume
volume69
Issue
issue5
Publisher
American Chemical Society (ACS)
Start Page
5944
End Page
5955
ISSN
0022-2623
NCID
AA00702411
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2026 The Authors.
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publisher
PubMed ID
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.1021/acs.jmedchem.5c03361
License
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 )