Literature DB >> 10796883

Survivin promotes cell proliferation in human hepatocellular carcinoma.

T Ito1, K Shiraki, K Sugimoto, T Yamanaka, K Fujikawa, M Ito, K Takase, M Moriyama, H Kawano, M Hayashida, T Nakano, A Suzuki.   

Abstract

Survivin is a recently described inhibitor of apoptosis. Because suppression of apoptosis is important for carcinogenesis and tumor growth, we investigated the expression and function of survivin in human hepatocellular carcinomas (HCCs). We have shown that 4 HCC cell lines and 7 out of 8 human HCC tissues expressed survivin messenger RNA (mRNA), whereas expression of survivin mRNA was not detected in normal liver and nontumor areas of these tissues using the reverse transcription polymerase chain reaction. Survivin was detected primarily in the nucleus by immunofluorescence staining of HCC cells. In addition, 14 of 20 (70%) HCC tissues showed positive nuclear staining for survivin, whereas nontumor tissues showed little detectable staining by immunohistochemistry. Survivin expression strongly correlated with the proliferation index but not significantly with the apoptosis index in HCC tissues. Therefore, we performed cell cycle analysis after survivin transfection and showed that overexpression of survivin resulted in a decrease in the G(0)/G(1) phase and an increase in the S phase in all 4 HCC cell lines. Furthermore, we have found that survivin interacted with cyclin-dependent kinase 4 (Cdk4) and overexpression of survivin released p21(WAF1/Cip1) (p21) from Cdk4. From these results, we conclude that survivin promotes cell proliferation by interacting with Cdk4 and releasing p21 from Cdk4. This may play an important role in carcinogenesis and progression of human HCCs.

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Year:  2000        PMID: 10796883     DOI: 10.1053/he.2000.6496

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  99 in total

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Journal:  Immunotherapy       Date:  2012-03       Impact factor: 4.196

2.  Expression of Survivin in pancreatic cancer and its correlation to expression of Bcl-2.

Authors:  Jian-Guo Qiao; Yu-Qing Zhang; Yu-Chun Yin; Zui Tan
Journal:  World J Gastroenterol       Date:  2004-09-15       Impact factor: 5.742

3.  Survivin antisense oligodeoxynucleotide inhibits growth of gastric cancer cells.

Authors:  Jian-Hui Yang; Yi-Chu Zhang; Hui-Qing Qian
Journal:  World J Gastroenterol       Date:  2004-04-15       Impact factor: 5.742

Review 4.  Nuclear or cytoplasmic expression of survivin: what is the significance?

Authors:  Fengzhi Li; Jie Yang; Nithya Ramnath; Milind M Javle; Dongfeng Tan
Journal:  Int J Cancer       Date:  2005-04-20       Impact factor: 7.396

5.  Survivin antisense compound inhibits proliferation and promotes apoptosis in liver cancer cells.

Authors:  De-Jian Dai; Cai-De Lu; Ri-Yong Lai; Jun-Ming Guo; Hua Meng; Wei-Sheng Chen; Jun Gu
Journal:  World J Gastroenterol       Date:  2005-01-14       Impact factor: 5.742

6.  Knockdown of survivin gene expression by RNAi induces apoptosis in human hepatocellular carcinoma cell line SMMC-7721.

Authors:  Sheng-Quan Cheng; Wen-Liang Wang; Wei Yan; Qing-Long Li; Li Wang; Wen-Yong Wang
Journal:  World J Gastroenterol       Date:  2005-02-07       Impact factor: 5.742

7.  Effect of siRNA targeting survivin gene on the biological behavior of hepatocellular carcinoma.

Authors:  Xin Lu; Qichang Zheng; Jun Xiong
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2005

8.  Expression of survivin, CDK4, Ki-67 and clinical significance in pediatric acute leukemia.

Authors:  Liuqing Zhang; Jing Liu; Hanhua Lin; Qun Hu; Aiguo Liu; Ying Hu
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2006

9.  Expression of survivin in human non-Hodgkin lymphoma and its correlation with proliferation and angiogenesis.

Authors:  Jiansha Li; Huanming Wu
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2006

10.  Survivin expression in early hepatocellular carcinoma and post-treatment with anti-cancer drug under hypoxic culture condition.

Authors:  Satoshi Mamori; Tadashi Asakura; Kiyoshi Ohkawa; Hisao Tajiri
Journal:  World J Gastroenterol       Date:  2007-10-28       Impact factor: 5.742

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