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Chinese Journal of Colorectal Diseases(Electronic Edition) ›› 2014, Vol. 03 ›› Issue (01): 24-27. doi: 10.3877/cma.j.issn.2095-3224.2014.01.06

Special Issue:

• Original Article • Previous Articles     Next Articles

USP22 and its potential targets in colorectal adenocarcinoma

Zheng JIANG1, Yan-long LIU2, Xi-shan WANG1,()   

  1. 1. Department of Colorectal Cancer Surgery, the Second Hospital of Harbin Medical University, the Colorectal Cancer Institute of the Heilongjiang Academy of Medical Sciences, Harbin 150086, China
  • Received:2014-02-02 Online:2014-02-25 Published:2014-02-25
  • Contact: Xi-shan WANG
  • About author:
    Corresponding author: WANG Xi-shan, Email:

Abstract:

Objective

To investigate the expression of USP22 and its potential targets in colorectal carcinoma.

Methods

82 cases of colorectal carcinoma were examined by quantitative RT-PCR.

Results

Statistical correlation analysis in mRNA level shown that USP22 was strongly correlated with BMI-1(r=0.790, P<0.0001), c-Myc(r=0.528, P<0.0001)and cyclin D2(r=0.657, P<0.0001), but not correlated with p16INK4a(r=0.103, P=0.358)or p14ARF(r=-0.039, P=0.731).

Conclusion

USP22 may activate BMI1 oncogene-driven pathway signature such as INK4a/ARF or Akt signature via activating the c-Myc-targeted genes such as cyclinD2, which may act as important role in tumor progression.

Key words: USP22, Colorectal cancer, Metastasis

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