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자료유형
학술저널
저자정보
Sun, Qi-Chang (Department of Biochemistry and Molecular Biology, Medical College of Soochow University) Liu, Mi-Bo (Department of Biochemistry and Molecular Biology, Medical College of Soochow University) Shen, Hong-Jie (The First Affiliated Hospital of Soochow University) Jiang, Zhi (Department of Biochemistry and Molecular Biology, Medical College of Soochow University) Xu, Lan (Department of Biochemistry and Molecular Biology, Medical College of Soochow University) Gao, Li-Ping (Department of Biochemistry and Molecular Biology, Medical College of Soochow University) Ni, Jian-Long (Department of Biochemistry and Molecular Biology, Medical College of Soochow University) Wu, Shi-Liang (Department of Biochemistry and Molecular Biology, Medical College of Soochow University)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제14권 제4호
발행연도
2013.1
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2,447 - 2,451 (5page)

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Objective: To study changes of tumor associated carbohydrate antigen (TACAs) expression and mRNA levels for tumor associated glycosyltransferases, and assess subcellular localizations of N-acetyl galactosyltransferases (GalNAc-Ts) in the K562 leukemia cell line after imatinib treatment. Methods: RT-PCR was performed to analyze the expression of glycosyltransferases which synthesize O-glycan in tumor-associated carbohydrate antigens (TCTAs). The expression of Tn antigen, T antigen and sialyl T antigen on K562 cell membranes was measured by flow cytometry after treatment with different concentrations of imatinib. Co-localization of GalNAc-Ts and ER (endoplasmic reticulum) was determined by confocal laser scanning microcopy. Results: Transcript expression levels of several glycosyltransferases related to TCTAs were decreased after imatinib ($0-0.3{\mu}M$) treatment. Expression of Tn antigen and T antigen was increased while that of sialyl T antigen was decreased. Co-localization of GalNAc-Ts and ER was reduced by $0.2{\mu}M$ of imatinib. Conclusion: Imatinib inhibited the expression of O-glycan related TACAs and several related glycosyltransferases, while decreasing the co-localization of GalNAc-Ts and ER and normalizing O-glycosylation in the K562 human leukemia cell.

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