Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34923
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    題名: Thiamet G as a Potential Treatment for Polycystic Kidney Disease
    作者: Su, Wen-Cheng
    Hung, Chi-Feng
    Wang, Yi-Chieh
    Peng, Hubert
    Huang, Wen-Hung
    Lo, Yi-Lun
    Lo, Yun-Hwa
    Chen, Yi-Cheng
    Su, Hsin-Hui
    Chen, Yung-Liang
    貢獻者: Yuan Pei Univ Med Technol, Dept Med Lab Sci & Biotechnol
    Chia yi Christian Hosp, Ditmanson Med Fdn, Dept Urol
    Natl Cheng Kung Univ, Coll Med, Dept Biochem & Mol Biol
    Acad Sinica, Inst Mol Biol
    Natl Yang Ming Chiao Tung Univ, Coll Med, Inst Pharmacol
    Kaohsiung Med Univ, Coll Life Sci, Dept Med & Appl Chem
    Natl Pingtung Univ Sci & Technol, Dept Vet Med
    Chia Nan Univ Pharm & Sci, Dept Pharm
    Yuan Pei Univ Sci & Technol, Dept Med Lab Sci & Biotechnol
    Chia Nan Univ Pharm & Sci, Dept Pharm
    關鍵詞: Autosomal dominant polycystic kidney disease
    ADPKD
    O-linked N-acetylglucosamine
    Thiamet G
    日期: 2023
    上傳時間: 2024-12-25 11:05:42 (UTC+8)
    出版者: INT INST ANTICANCER RESEARCH
    摘要: Background/Aim: Autosomal dominant polycystic kidney disease (ADPKD) is a prevalent genetic disorder primarily caused by mutations in Pkd1 (PC1), which account for the majority of ADPKD cases. These mutations contribute to the formation of cysts in the kidneys and other organs, ultimately leading to renal failure. Unfortunately, there are currently no available preventive treatments for this disease. Materials and Methods: In this study, we utilized Pkd1-knockdown mice and cells to investigate the potential involvement of O-GlcNAcylation in the progression of PKD. Additionally, we examined the effects of thiamet G, an inhibitor of O-GlcNAcase (OGA), on PKD mice. Results: Our findings indicate that both O-GlcNAcylation and OGT (O-GlcNAc transferase) were downregulated in the renal tissues of Pkd1-silenced mice. Furthermore, OGlcNAcylation was shown to regulate the stability and function of the C-terminal cytoplasmic tail (CTT) of PC1. Treatment of PKD mice with thiamet G resulted in a reduction of renal cytogenesis in these animals. Conclusion: These results highlight the unique role of O-GlcNAcylation in the development of cyst formation in PKD and propose it as a potential therapeutic target for the treatment of PKD.
    關聯: In Vivo, v.37, n.6, pp.2524-2532
    顯示於類別:[Dept. of Pharmacy] Periodical Articles

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