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Article

HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility

  • Authors:
    • Yuchun Li
    • Kaijuan Wang
    • Liping Dai
    • Peng Wang
    • Chunhua Song
    • Jianxiang Shi
    • Pengfei Ren
    • Hua Ye
    • Jianying Zhang
  • View Affiliations / Copyright

    Affiliations: Department of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou 450001, P.R. China, Henan Key Laboratory of Tumor Epidemiology, Zhengzhou University, Zhengzhou, Henan 450052, P.R. China, Department of Biological Sciences, University of Texas, El Paso, TX 79968, USA
  • Pages: 358-364
    |
    Published online on: May 23, 2012
       https://doi.org/10.3892/ol.2012.728
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Abstract

CIP2A is a human oncoprotein that inhibits PP2A and stabilizes c-myc in human malignancies. Autoantibodies to CIP2A protein have been reported to be present in higher levels in sera from patients with hepatocellular carcinoma (HCC) than in sera of healthy individuals. The CIP2A gene has been demonstrated as a potential cancer susceptibility gene. To elucidate whether common CIP2A variants are associated with HCC susceptibility, we conducted a case-control study comprising 233 cases of HCC and 280 controls matched on age, gender and ethnicity in the Chinese Han population. Two haplotype-tagging single nucleotide polymorphisms (htSNPs) (rs2278911 and rs4855656) from the HapMap database were analyzed, which provide an almost complete coverage of the genetic variations in the CIP2A gene. We found that neither of these htSNPs and haplotypes were associated with the risk of HCC. However, an interaction was observed between hepatitis virus B and C infection (HBV and HCV) and the C carriers (TC or CC) of rs2278911 on HCC risk (OR=12.35; 95% CI, 4.93-19.87). No such association was found for rs4855656. Our study also demonstrated that two htSNPs (rs2278911 and rs4855656) in the CIP2A gene are not associated with the risk of HCC. HBV and HCV infection was found to exert a synergistic effect on the risk of HCC in individuals with the C carriers (TC or CC) of rs2278911 in the Chinese Han population.
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Copy and paste a formatted citation
Spandidos Publications style
Li Y, Wang K, Dai L, Wang P, Song C, Shi J, Ren P, Ye H and Zhang J: HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility. Oncol Lett 4: 358-364, 2012.
APA
Li, Y., Wang, K., Dai, L., Wang, P., Song, C., Shi, J. ... Zhang, J. (2012). HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility. Oncology Letters, 4, 358-364. https://doi.org/10.3892/ol.2012.728
MLA
Li, Y., Wang, K., Dai, L., Wang, P., Song, C., Shi, J., Ren, P., Ye, H., Zhang, J."HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility". Oncology Letters 4.2 (2012): 358-364.
Chicago
Li, Y., Wang, K., Dai, L., Wang, P., Song, C., Shi, J., Ren, P., Ye, H., Zhang, J."HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility". Oncology Letters 4, no. 2 (2012): 358-364. https://doi.org/10.3892/ol.2012.728
Copy and paste a formatted citation
x
Spandidos Publications style
Li Y, Wang K, Dai L, Wang P, Song C, Shi J, Ren P, Ye H and Zhang J: HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility. Oncol Lett 4: 358-364, 2012.
APA
Li, Y., Wang, K., Dai, L., Wang, P., Song, C., Shi, J. ... Zhang, J. (2012). HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility. Oncology Letters, 4, 358-364. https://doi.org/10.3892/ol.2012.728
MLA
Li, Y., Wang, K., Dai, L., Wang, P., Song, C., Shi, J., Ren, P., Ye, H., Zhang, J."HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility". Oncology Letters 4.2 (2012): 358-364.
Chicago
Li, Y., Wang, K., Dai, L., Wang, P., Song, C., Shi, J., Ren, P., Ye, H., Zhang, J."HapMap-based study of CIP2A gene polymorphisms and HCC susceptibility". Oncology Letters 4, no. 2 (2012): 358-364. https://doi.org/10.3892/ol.2012.728
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