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B4GALT1 基因敲低抑制 hedgehog 通路并逆转人白血病 K562/阿霉素耐药细胞系的多药耐药性。

B4GALT1 gene knockdown inhibits the hedgehog pathway and reverses multidrug resistance in the human leukemia K562/adriamycin-resistant cell line.

机构信息

Department of Laboratory Medicine, College of Laboratory Medicine, Dalian Medical University, Dalian, Liaoning Province, People's Republic of China.

出版信息

IUBMB Life. 2012 Nov;64(11):889-900. doi: 10.1002/iub.1080. Epub 2012 Sep 29.

Abstract

B4GALT1 gene encodes type II membrane-bound glycoprotein, named β-1, 4-galactosyltransferase 1 (β1, 4-Gal-T1), which can transfer galactose to acceptor sugars. B4GALT1 gene plays important roles in physiological process and disease development. In this study, we investigate the possible role and mechanism of B4GALT1 gene in multidrug resistance of human leukemia cell line. Significantly, higher expression of B4GALT1 was observed in adriamycin-resistant (ADR) K562 cell line (K562/ADR) than that in K562 cell line by real-time polymerase chain reaction and Western blotting. The activity of β1, 4-Gal-T1 enzyme, and Galβ-1,4GlcNAc structures on cell membrane glycoproteins was found at higher levels in K562/ADR cells than those in K562 cells. Further analysis of the B4GALT1 deregulation after using RNA interference approach showed that the silencing of B4GALT1 in K562/ADR cells resulted in increased sensitivity to chemotherapeutic drugs both in vitro and in vivo. The activity of the hedgehog signaling pathway affected the chemosensitivity of K562/ADR cells and was downregulated in K562/ADR cells with suppression of B4GALT1 gene. We hypothesize that B4GALT1 is responsible for the overcoming multidrug resistance in human leukemia therapy via regulating the activity of the hedgehog signaling pathway.

摘要

B4GALT1 基因编码 II 型膜结合糖蛋白,命名为β-1,4-半乳糖基转移酶 1(β1,4-Gal-T1),它可以将半乳糖转移到受体糖上。B4GALT1 基因在生理过程和疾病发展中发挥重要作用。在这项研究中,我们研究了 B4GALT1 基因在人白血病细胞系多药耐药中的可能作用和机制。通过实时聚合酶链反应和 Western blot 分析,我们发现阿霉素耐药(ADR)K562 细胞系(K562/ADR)中 B4GALT1 的表达明显高于 K562 细胞系。在 K562/ADR 细胞中,β1,4-Gal-T1 酶的活性以及细胞膜糖蛋白上的 Galβ-1,4GlcNAc 结构水平均高于 K562 细胞。进一步分析 RNA 干扰方法下调 B4GALT1 后的结果表明,沉默 K562/ADR 细胞中的 B4GALT1 可显著增加细胞对化疗药物的敏感性,无论是在体外还是体内。 hedgehog 信号通路的活性影响 K562/ADR 细胞的化疗敏感性,而在抑制 B4GALT1 基因后,K562/ADR 细胞中的 hedgehog 信号通路活性被下调。我们假设 B4GALT1 通过调节 hedgehog 信号通路的活性,负责克服人类白血病治疗中的多药耐药。

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