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Sequence mutations of the substrate binding pocket of stem cell factor and multidrug resistance protein ABCG2 in renal cell cancer: A possible link to treatment resistance

机译:肾细胞癌中干细胞因子和多药耐药蛋白ABCG2的底物结合口袋的序列突变:可能与治疗耐药性有关

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摘要

ABCG2 is a multidrug cellular transport protein that is associated with resistance to certain treatments in patients, particularly anticancer treatment. The tumor-protective properties of ABCG2 expression are reported to be a feature of a subset of stem cell-like tumor cells. While protection against chemotherapy has been well analyzed, the role of ABCG2 in the treatment with tyrosine kinase inhibitors is only partially understood. Tyrosine kinase inhibitors are currently the main treatment option in irresectable renal cell carcinomas. To investigate possible underlying sequence variations in the ABCG2 gene with relevance to the functional properties of the protein, 36 patient samples were analyzed. Using sequence analysis and single-nucleotide polymorphism databases, sequence variations in the highly conserved domains of the binding pocket of ABCG2 were analyzed. The resulting variations were used for computational protein prediction algorithms to identify conformational alterations. A relevant shift from A to G at position 1376 (resulting in Y→C at 459 aa) was identified and found to be present in 8.3% of the patients. These patients are currently in follow-up after resection, thus, further analysis will reveal whether this mutation has relevance to treatment efficacy.
机译:ABCG2是一种多药细胞转运蛋白,与患者对某些治疗方法的抗性有关,尤其是抗癌治疗。据报道,ABCG2表达的肿瘤保护特性是干细胞样肿瘤细胞的一个子集。虽然已经很好地分析了对化学疗法的保护作用,但对ABCG2在酪氨酸激酶抑制剂治疗中的作用仅作了部分了解。酪氨酸激酶抑制剂目前是不可切除的肾细胞癌的主要治疗选择。为了研究与蛋白质的功能特性相关的ABCG2基因中潜在的潜在序列变异,分析了36个患者样品。使用序列分析和单核苷酸多态性数据库,分析了ABCG2结合口袋高度保守的结构域中的序列变异。产生的变异用于计算蛋白质预测算法,以识别构象改变。确定了在位置1376处从A到G的相关变化(导致459aa处的Y→C),发现存在8.3%的患者。这些患者在切除后目前正在随访中,因此,进一步的分析将揭示该突变是否与治疗效果相关。

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