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Sper/NO-induced reversible proliferation inhibition and cycle arrests associated with a micronucleus induction in HSG cells.
https://repo.qst.go.jp/records/43063
https://repo.qst.go.jp/records/4306375828f28-dea0-4f33-929d-0d6bb6900770
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2003-03-24 | |||||
タイトル | ||||||
タイトル | Sper/NO-induced reversible proliferation inhibition and cycle arrests associated with a micronucleus induction in HSG cells. | |||||
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 |
Shao, Chunlin
× Shao, Chunlin× Furusawa, Yoshiya× Aoki, Mizuho× Shao Chunlin× 古澤 佳也× 青木 瑞穂 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Nitric oxide (NO) is an important messenger molecule with multiple biological activities. In the present study, sper/NO, a NO generator, showed a biphasic effect on the proliferation of human salivary gland neoplastic (HSG) cells. Sper/NO of less than 20 ugr;M stimulated cells to depart from the G2/M phase and so enhanced cell division and cell proliferation. But sper/NO at higher concentrations restrained cell proliferation and blocked cell-cycle progression. Cells were mainly arrested in the G2/M phase and S phase when they were treated with 100-200 and 300-500 ugr;M sper/NO, respectively. A special S-phase peak was detected in a histogram of the cell-phase distribution of sper/NO-treated HSG. When the concentration of sper/NO increased, the S-phase peak shifted from early the G2/M-phase to later the G1-S-phase boundary. Sper/NO-induced cell-cycle arrests were reversible when the cells were released from NO stress for 48h and hence cell proliferation was recovered. In addition, micronucleus, but no apoptosis, was produced in the sper/NO-treated cells, and its yield tended to a saturation value with increasing concentrations of sper/NO. The sper/NO-induced effects were effectively eliminated or reduced by treating cells with PTIO, a NO-specific scavenger, indicating that NO is the main source of these effects. | |||||
書誌情報 |
Nitric Oxide : Biology and Chemistry 巻 8, p. 83-88, 発行日 2003-03 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1089-8603 |