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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

Aberrant expression of serine/threonine kinase Pim-3 in hepatocellular carcinoma development and its role in the proliferation of human hepatoma cell lines

http://hdl.handle.net/2297/6664
http://hdl.handle.net/2297/6664
b818deb1-93b4-425b-9719-40ec9b9e41c8
名前 / ファイル ライセンス アクション
CA-PR-MUKAIDA-N-209.pdf CA-PR-MUKAIDA-N-209.pdf (919.8 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 Aberrant expression of serine/threonine kinase Pim-3 in hepatocellular carcinoma development and its role in the proliferation of human hepatoma cell lines
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 Fujii, Chifumi

× Fujii, Chifumi

WEKO 17028
研究者番号 10361982

Fujii, Chifumi

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Nakamoto, Yasunari

× Nakamoto, Yasunari

WEKO 108
e-Rad 40293352
研究者番号 40293352

Nakamoto, Yasunari

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Lu, Peirong

× Lu, Peirong

WEKO 47503

Lu, Peirong

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Tsuneyama, Koichi

× Tsuneyama, Koichi

WEKO 47504

Tsuneyama, Koichi

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Popivanova, Boryana K.

× Popivanova, Boryana K.

WEKO 47505

Popivanova, Boryana K.

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Kaneko, Shuichi

× Kaneko, Shuichi

WEKO 62
e-Rad 60185923
金沢大学研究者情報 60185923
研究者番号 60185923

Kaneko, Shuichi

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Mukaida, Naofumi

× Mukaida, Naofumi

WEKO 49
e-Rad 30182067
金沢大学研究者情報 30182067
研究者番号 30182067

Mukaida, Naofumi

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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がん病態制御
書誌情報 International Journal of Cancer

巻 114, 号 2, p. 209-218, 発行日 2005-03-20
ISSN
収録物識別子タイプ ISSN
収録物識別子 1097-0215
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1002/ijc.20719
出版者
出版者 Wiley-Liss
抄録
内容記述タイプ Abstract
内容記述 Most cases of human hepatocellular carcinoma develop after persistent chronic infection with human hepatitis B virus or hepatitis C virus, and host responses are presumed to have major roles in this process. To recapitulate this process, we have developed the mouse model of hepatocellular carcinoma using hepatitis B virus surface antigen transgenic mice. To identify the genes associated with hepatocarcinogenesis in this model, we compared the gene expression patterns between pre-malignant lesions surrounded by hepatocellular carcinoma tissues and control liver tissues by using a fluorescent differential display analysis. Among the genes that were expressed differentially in the pre-malignant lesions, we focused on Pim-3, a member of a proto-oncogene Pim family, because its contribution to hepatocarcinogenesis remains unknown. Moreover, the unavailability of the nucleotide sequence of full-length human Pim-3 cDNA prompted us to clone it from the cDNA library constructed from a human hepatoma cell line, HepG2. The obtained 2,392 bp human Pim-3 cDNA encodes a predicted open reading frame consisting of 326 amino acids. Pim-3 mRNA was selectively expressed in human hepatoma cell lines, but not in normal liver tissues. Moreover, Pim-3 protein was detected in human hepatocellular carcinoma tissues and cell lines but not in normal hepatocytes. Furthermore, cell proliferation was attenuated and apoptosis was enhanced in human hepatoma cell lines by the ablation of Pim-3 gene with RNA interference. These observations suggest that aberrantly expressed Pim-3 can cause autonomous cell proliferation or prevent apoptosis in hepatoma cell lines. © 2004 Wiley-Liss, Inc.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
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