Literature DB >> 28685058

Cell division cycle 34 is highly expressed in hepatitis C virus-positive hepatocellular carcinoma with favorable phenotypes.

Keiko Takagi1, Tadatoshi Takayama1, Yutaka Midorikawa1, Hiromasa Hasegawa2, Takanaga Ochiai2, Masamichi Moriguchi1, Tokio Higaki1, Masayoshi Soma3, Hiroki Nagase4, Kyoko Fujiwara3.   

Abstract

Despite tremendous efforts to develop curative agents, there are few effective drugs for the treatment of hepatocellular carcinoma (HCC). This is predominantly due to the variations in individual HCC cases. As numerous HCC cases have no mutations in known tumor-associated genes, identification of novel genes involved in the development and progression of human cancers is considered to be an urgent issue. In the present study, surgical specimens of HCC were analyzed for the expression patterns of ubiquitin-conjugating enzyme, cell division cycle 34 (CDC34), which is hypomethylated in its promoter region and exhibits elevated expression levels in mouse skin tumors. The results of the current study clearly indicated that the elevated CDC34 expression level in cancerous regions was significantly associated with favorable clinicopathological features, such as reduced alanine aminotransferase (ALT) levels and histological grades. Similarly, a higher T/N ratio, which is the ratio of CDC34 expression in HCCs to that in non-tumorous tissues, was significantly associated with favorable features, such as a lower indocyanin green retention rate after 15 min (ICG15R), reduced α-fetoprotein and smaller tumor size. These results indicate that the CDC34 expression level in HCC is a marker for predicting the HCC prognosis and that CDC34 acts as a tumor suppressor.

Entities:  

Keywords:  cell division cycle 34; clinicopathological feature; hepatitis C virus-positive hepatocellular carcinoma; prognostic marker; tumor suppressor

Year:  2017        PMID: 28685058      PMCID: PMC5492648          DOI: 10.3892/br.2017.912

Source DB:  PubMed          Journal:  Biomed Rep        ISSN: 2049-9434


  26 in total

1.  Hepatitis C virus core protein inhibits mitochondrial electron transport and increases reactive oxygen species (ROS) production.

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Journal:  J Biol Chem       Date:  2005-09-08       Impact factor: 5.157

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Authors:  Alejandro Forner; Josep M Llovet; Jordi Bruix
Journal:  Lancet       Date:  2012-02-20       Impact factor: 79.321

5.  Risk factors contributing to early and late phase intrahepatic recurrence of hepatocellular carcinoma after hepatectomy.

Authors:  Hiroshi Imamura; Yutaka Matsuyama; Eiji Tanaka; Takao Ohkubo; Kiyoshi Hasegawa; Shinichi Miyagawa; Yasuhiko Sugawara; Masami Minagawa; Tadatoshi Takayama; Seiji Kawasaki; Masatoshi Makuuchi
Journal:  J Hepatol       Date:  2003-02       Impact factor: 25.083

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Journal:  N Engl J Med       Date:  2008-07-24       Impact factor: 91.245

7.  The B-type cyclin kinase inhibitor p40SIC1 controls the G1 to S transition in S. cerevisiae.

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Journal:  Cell       Date:  1994-10-21       Impact factor: 41.582

8.  Hepatitis C virus-induced activation of β-catenin promotes c-Myc expression and a cascade of pro-carcinogenetic events.

Authors:  M R Higgs; H Lerat; J-M Pawlotsky
Journal:  Oncogene       Date:  2012-10-29       Impact factor: 9.867

Review 9.  HCV and oxidative stress in the liver.

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Journal:  Viruses       Date:  2013-01-28       Impact factor: 5.048

10.  Investigating the mechanism of hepatocellular carcinoma progression by constructing genetic and epigenetic networks using NGS data identification and big database mining method.

Authors:  Cheng-Wei Li; Ping-Yao Chang; Bor-Sen Chen
Journal:  Oncotarget       Date:  2016-11-29
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  2 in total

1.  Structural insights into E1 recognition and the ubiquitin-conjugating activity of the E2 enzyme Cdc34.

Authors:  Katelyn M Williams; Shuo Qie; James H Atkison; Sabrina Salazar-Arango; J Alan Diehl; Shaun K Olsen
Journal:  Nat Commun       Date:  2019-07-24       Impact factor: 14.919

2.  Systematic identification of CDC34 that functions to stabilize EGFR and promote lung carcinogenesis.

Authors:  Xin-Chun Zhao; Gui-Zhen Wang; Zhe-Sheng Wen; Yong-Chun Zhou; Qian Hu; Bin Zhang; Li-Wei Qu; San-Hui Gao; Jie Liu; Liang Ma; Yan-Fei Zhang; Chen Zhang; Hong Yu; Da-Lin Zhang; Min Wang; Chang-Li Wang; Yun-Chao Huang; Zhi-Hua Liu; Yong Zhao; Liang Chen; Guang-Biao Zhou
Journal:  EBioMedicine       Date:  2020-02-27       Impact factor: 8.143

  2 in total

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