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Article

Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice

  • Authors:
    • Cheng‑Hsu Chen
    • Yeh‑Han Wang
    • Shang‑Feng Tsai
    • Tung‑Min Yu
    • Shih‑Yin Chen
    • Fuu‑Jen Tsai
  • View Affiliations / Copyright

    Affiliations: Department of Medical Research, Division of Basic Medical Sciences, Taichung Veterans General Hospital, Taichung 40705, Taiwan, R.O.C., Department of Anatomical Pathology, Taipei Institute of Pathology, School of Medicine, National Yang‑Ming University, 11221 Taipei, Taiwan, R.O.C., Department of Internal Medicine, Division of Nephrology, Taichung Veterans General Hospital, Taichung 40705, Taiwan, R.O.C., School of Chinese Medicine, China Medical University, Taichung 40402, Taiwan, R.O.C.
  • Pages: 3139-3146
    |
    Published online on: August 20, 2019
       https://doi.org/10.3892/etm.2019.7919
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Abstract

Diabetes mellitus (DM) is a complex disease caused by absolute or relative insulin deficiency. The C57BLKsJ‑db/db mouse model is a useful animal model for studying type 2 DM (T2DM). The present study investigated the association between an antizyme inhibitor 1 (AZIN1) gene polymorphism (rs1062048) and T2DM susceptibility in 2,270 Taiwanese individuals (570 patients with T2DM and 1,700 controls). Additionally, the present study investigated AZIN1 gene and protein expression in the liver tissues of mice in three age groups (4, 16 and 32 weeks) through reverse transcription‑quantitative PCR, western blotting and immunohistochemistry. The data indicated that the genotype frequency distribution of the rs1062048 single‑nucleotide polymorphism differed significantly between the patients with T2DM and controls (P<0.05). Furthermore, gene and protein expression levels of AZIN1 were significantly lower in early stage and late stage T2DM mouse liver samples than in control samples. Overall, the data suggested that AZIN1 expression is involved in T2DM development.
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Copy and paste a formatted citation
Spandidos Publications style
Chen CH, Wang YH, Tsai SF, Yu TM, Chen SY and Tsai FJ: Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice. Exp Ther Med 18: 3139-3146, 2019.
APA
Chen, C., Wang, Y., Tsai, S., Yu, T., Chen, S., & Tsai, F. (2019). Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice. Experimental and Therapeutic Medicine, 18, 3139-3146. https://doi.org/10.3892/etm.2019.7919
MLA
Chen, C., Wang, Y., Tsai, S., Yu, T., Chen, S., Tsai, F."Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice". Experimental and Therapeutic Medicine 18.4 (2019): 3139-3146.
Chicago
Chen, C., Wang, Y., Tsai, S., Yu, T., Chen, S., Tsai, F."Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice". Experimental and Therapeutic Medicine 18, no. 4 (2019): 3139-3146. https://doi.org/10.3892/etm.2019.7919
Copy and paste a formatted citation
x
Spandidos Publications style
Chen CH, Wang YH, Tsai SF, Yu TM, Chen SY and Tsai FJ: Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice. Exp Ther Med 18: 3139-3146, 2019.
APA
Chen, C., Wang, Y., Tsai, S., Yu, T., Chen, S., & Tsai, F. (2019). Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice. Experimental and Therapeutic Medicine, 18, 3139-3146. https://doi.org/10.3892/etm.2019.7919
MLA
Chen, C., Wang, Y., Tsai, S., Yu, T., Chen, S., Tsai, F."Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice". Experimental and Therapeutic Medicine 18.4 (2019): 3139-3146.
Chicago
Chen, C., Wang, Y., Tsai, S., Yu, T., Chen, S., Tsai, F."Antizyme inhibitor 1 genetic polymorphisms associated with diabetic patients validated in the livers of diabetic mice". Experimental and Therapeutic Medicine 18, no. 4 (2019): 3139-3146. https://doi.org/10.3892/etm.2019.7919
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