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  1. H-1. がん進展制御研究所
  2. h-1 10. 学術雑誌掲載論文
  3. 1. 査読済論文

Effect of gemcitabine on the expression of apoptosis-related genes in human pancreatic cancer cells.

http://hdl.handle.net/2297/11753
http://hdl.handle.net/2297/11753
0c437fab-3242-4ad5-90fd-3bffb6a98d42
名前 / ファイル ライセンス アクション
CA-PR-MINAMOTO-T-1597.pdf CA-PR-MINAMOTO-T-1597.pdf (365.7 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-05
タイトル
タイトル Effect of gemcitabine on the expression of apoptosis-related genes in human pancreatic cancer 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
著者 Jiang, Pei-Hong

× Jiang, Pei-Hong

WEKO 47622

Jiang, Pei-Hong

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Motoo, Yoshiharu

× Motoo, Yoshiharu

WEKO 21362
e-Rad 80210095
研究者番号 80210095

Motoo, Yoshiharu

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Sawabu, Norio

× Sawabu, Norio

WEKO 21711
e-Rad 90019969
研究者番号 90019969

Sawabu, Norio

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Minamoto, Toshinari

× Minamoto, Toshinari

WEKO 65
e-Rad 50239323
金沢大学研究者情報 50239323
研究者番号 50239323

Minamoto, Toshinari

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提供者所属
内容記述タイプ Other
内容記述 金沢大学がん研究所
書誌情報 World Journal of Gastroenterology

巻 12, 号 10, p. 1597-1602, 発行日 2006-03-14
ISSN
収録物識別子タイプ ISSN
収録物識別子 1007-9327
NCID
収録物識別子タイプ NCID
収録物識別子 AA11690631
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 https://doi.org/10.3748/wjg.v12.i10.1597
出版者
出版者 WJG Press
抄録
内容記述タイプ Abstract
内容記述 Aim: To investigate the expression of genes involved in the gemcitabine-induced cytotoxicity in human pancreatic cancer cells. Methods: A human pancreatic cancer cell line, PANC-1, was cultured. 1 × 104 PANC-1 cells were plated in 96-well microtiter plates. After being incubated for 24 h, gemcitabine was added to the medium at concentrations ranging 2.5 -1 000 mg/L. The AlamarBlue dye method was used for cell growth analysis. DNA fragmentation was quantitatively assayed using a DNA fragmentation enzyme-linked immunosorbent assay (ELISA) kit. PAP and TP53INP1 mRNA expression was determined using the reverse transcription-polymerase chain reaction with semi-quantitative analysis. The expression of GSK-3β and phospho-GSK-3β proteins was examined with Western blot analysis. Results: The IC50 for the drug after a 48-h exposure to gemcitabine was 16 mg/L. The growth of PANC-1 cells was inhibited by gemcitabine in a concentration-dependent manner (P< 0.0001) and the cell growth was also inhibited throughout the time course (P<0.0001). The DNA fragmentation rate in the gemcitabine-treated group at 48 h was 44.7 %, whereas it was 25.3 % in the untreated group. The PAP mRNA expression was decreased after being treated with gemcitabine, whereas the TP53INP1 mRNA was increased by the gemcitabine treatment. Western blot analysis showed that phospho-GSK-3βser9 was induced by the gemcitabine treatment. Conclusion: Gemcitabine suppresses PANC-1 cell proliferation and induces apoptosis. Apoptosis is considered to be associated with the inhibition of PAP and GSK-3β, and the activation of TP53INP1 and pospho-GSK-3βser9. © 2006 The WJG Press. All rights reserved.
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
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