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Lectin array and glycogene expression analyses of ovarian cancer cell line A2780 and its cisplatin-resistant derivate cell line A2780-cp

机译:卵巢癌细胞系A2780及其对顺铂耐药的衍生细胞系A2780-cp的凝集素阵列和糖基因表达分析

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Background Ovarian cancer is one of the most lethal gynecological malignancies, in which platinum resistance is a common cause of its relapse and death. Glycosylation has been reported to be involved in drug resistance, and glycomic analyses of ovarian cancer may improve our understanding of the mechanisms underlying cancer cell drug resistance and provide potential biomarkers and therapeutic targets. Methods The serous ovarian cancer cell line A2780 and its platinum-resistant counterpart A2780-cp were used in this study. We performed a lectin array analysis to compare the glycosylation patterns of the two cell lines, a gene expression array was employed to probe the differences in glycogenes. Furthermore, the results were verified by lectin blots. Results A2780-cp cell exhibited stronger intensities of Lens culinaris (LCA) Canavalia ensiformis (ConA), and Lycopersicon esculentum (LEL) and weaker intensities of Sambucus nigra (SNA) lectins. The gene expression array analysis revealed increased expression of Fut8, B3gnt4, B3gnt5, B4galt2 and decreased expression of Fut1 and ST6GalNAc 6 expression were evident in the A2780-cp cells. The lectin blot confirmed the differences in LCA, ConA, SNA and LEL between the A2780 and A2780-cp cells. Conclusions The combination of the lectin and gene expression analyses showed that the levels of core fucosylation and poly-LacNAc were increased in the A2780-cp cells and the levels of Fuc α1-2(gal β1-4) GlcNAc and α2-6-linked sialic structures were decreased in the A2780-cp cells. These glycans represent potential biomarkers and might be involved in the mechanism of drug resistance in ovarian cancer.
机译:背景技术卵巢癌是最致命的妇科恶性肿瘤之一,其中铂耐药是其复发和死亡的常见原因。据报道糖基化与耐药性有关,对卵巢癌的糖类分析可以增进我们对癌细胞耐药性机制的了解,并提供潜在的生物标志物和治疗靶标。方法采用浆液性卵巢癌细胞系A2780及其对铂耐药的A2780-cp。我们进行了凝集素阵列分析以比较两种细胞系的糖基化模式,采用基因表达阵列来探查糖基因的差异。此外,结果通过凝集素印迹证实。结果A2780-cp细胞表现出较弱的加拿大扁豆(LCA),Canavalia ensiformis(ConA)和番茄(Lycopersicon esculentum)(LEL)强度,而黑接骨木(SNA)凝集素强度较弱。基因表达阵列分析显示在A2780-cp细胞中Fut8,B3gnt4,B3gnt5,B4galt2表达增加,而Fut1和ST6GalNAc 6表达减少。凝集素印迹证实了A2780和A2780-cp细胞之间LCA,ConA,SNA和LEL的差异。结论凝集素和基因表达分析的结合表明,A2780-cp细胞的核心岩藻糖基化水平和poly-LacNAc水平升高,Fucα1-2(galβ1-4)GlcNAc和α2-6-linked水平升高在A2780-cp细胞中唾液酸结构减少。这些聚糖代表潜在的生物标志物,并可能参与卵巢癌的耐药机制。

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