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Novel acridine-based N-acyl-homoserine lactone analogs induce endoreduplication in the human oral squamous carcinoma cell line SAS.
https://repo.qst.go.jp/records/46643
https://repo.qst.go.jp/records/466434d115ad0-b3e6-483f-bc31-c936accfa208
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2013-11-26 | |||||
タイトル | ||||||
タイトル | Novel acridine-based N-acyl-homoserine lactone analogs induce endoreduplication in the human oral squamous carcinoma cell line SAS. | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Chai, H
× Chai, H× Hazawa, Masaharu× Hosokawa, Y× Igarashi, J× Suga, H× Kashiwakura, Ikuo× 羽澤 勝治 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The cytotoxicity of novel acridine-based N-acyl-homoserine lactone (AHL) analogs was investigated on the human oral squamous carcinoma cell line SAS. One analog induced G2/M phase arrest at 5.3-10.6 µM and induced polyploidy at a higher dose (21.2 µM). Importantly, treatment of SAS cells with a combination of the AHL analog and the Jun N-terminal kinase (JNK) inhibitor, SP600125, prevented mitosis and induced polyploidy. The AHL analog synergized with X-irradiation to inhibit clonogenic survival of SAS cells; however, its radiosensitizing effects were relative to not X-irradiation-induced apoptosis but mitotic failure following enhanced expression of Aurora A and B. These results suggest that the active AHL analog showed growth-suppressive and radiosensitizing effects, which involve polyploidy followed by G2/M accumulation and atypical cell death in the SAS cell line. | |||||
書誌情報 |
Biological & Pharmaceutical Bulletin 巻 35, 号 8, p. 1257-63, 発行日 2012-11 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0918-6158 |