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Association of relapse-linked ARID5B single nucleotide polymorphisms with drug resistance in B-cell precursor acute lymphoblastic leukemia cell lines

机译:复发联系的ARID5B单核苷酸多态性与B细胞前体急性淋巴细胞白血病细胞系耐药性的单核苷酸多态性

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摘要

Abstract Background The genetic variants of the ARID5B gene have recently been reported to be associated with disease susceptibility and treatment outcome in childhood acute lymphoblastic leukemia (ALL). However, few studies have explored the association of ARID5B with sensitivities to chemotherapeutic agents. Methods We genotyped susceptibility-linked rs7923074 and rs10821936 as well as relapse-linked rs4948488, rs2893881, and rs6479778 of ARDI5B by direct sequencing of polymerase chain reaction (PCR) products in 72 B-cell precursor-ALL (BCP-ALL) cell lines established from Japanese patients. We also quantified their ARID5B expression levels by real-time reverse transcription PCR, and determined their 50% inhibitory concentration (IC50) values by alamarBlue assays in nine representative chemotherapeutic agents used for ALL treatment. Results No significant associations were observed in genotypes of the susceptibility-linked single nucleotide polymorphisms (SNPs) and the relapsed-linked SNPs with ARID5B gene expression levels. Of note, IC50 values of vincristine (VCR) (median IC50: 39.6 ng/ml) in 12 cell lines with homozygous genotype of risk allele (C) in the relapse-linked rs4948488 were significantly higher (p = 0.031 in Mann–Whitney U test) than those (1.04 ng/ml) in 60 cell lines with heterozygous or homozygous genotypes of the non-risk allele (T). Furthermore, the IC50 values of mafosfamide [Maf; active metabolite of cyclophosphamide (CY)] and cytarabine (AraC) tended to be associated with the genotype of rs4948488. Similar associations were observed in genotypes of the relapse-linked rs2893881 and rs6479778, but not in those of the susceptibility-linked rs7923074 and rs10821936. In addition, the IC50 values of methotrexate (MTX) were significantly higher (p = 0.023) in 36 cell lines with lower ARID5B gene expression (median IC50: 37.1 ng/ml) than those in the other 36 cell lines with higher expression (16.9 ng/ml). Conclusion These observations in 72 BCP-ALL cell lines suggested that the risk allele of the relapse-linked SNPs of ARID5B may be involved in a higher relapse rate because of resistance to chemotherapeutic agents such as VCR, CY, and AraC. In addition, lower ARID5B gene expression may be associated with MTX resistance.
机译:摘要背景最近报道的ARID5B基因的遗传变异为与疾病易感性和治疗效果在儿童急性淋巴细胞白血病(ALL)相关联。然而,很少有研究探讨ARID5B协会与敏感性化疗药物。方法我们基因型ARDI5B易感性联rs7923074和rs10821936以及复发联rs4948488,rs2893881,和rs6479778由(PCR)产物在72 B细胞前体ALL(BCP-ALL)细胞系建立的聚合酶链反应的直接测序从日本患者。我们还通过实时逆转录PCR定量其ARID5B表达水平,并确定在用于ALL治疗9代表化疗剂通过阿尔玛蓝测定其50%抑制浓度(IC 50)值。结果未显著协会易感性联的单核苷酸多态性(SNP),并与ARID5B基因表达水平的复发联的SNP基因型中观察到。值得注意的是,长春新碱(VCR)的IC 50个值(中值IC50:39.6纳克/毫升)与(C)在复发联rs4948488风险等位基因的纯合子的基因型12个细胞系是显著升高(P在曼 - 惠特尼U = 0.031测试)比(1.04毫微克/毫升)与非风险等位基因(T)的杂合或纯基因型60个的细胞系。此外,马磷酰胺的IC 50个值[MAF;环磷酰胺的活性代谢物(CY)〕和阿糖胞苷(阿糖胞苷)趋于与rs4948488的基因型相关联。在复发联rs2893881和rs6479778的基因型观察到类似的协会,而不是在那些敏感性联rs7923074和rs10821936的。此外,(MTX)氨甲蝶呤的IC50值分别为显著更高(P = 0.023)中具有较低ARID5B基因表达36个细胞系(中值IC50:37.1纳克/毫升)比与高表达的其它36个细胞系(16.9纳克/毫升)。结论在72 BCP-ALL细胞系这些观察结果表明,ARID5B的复发联SNP的风险等位基因可能涉及更高的复发率,因为对化疗剂诸如VCR,CY,和阿糖胞苷的阻力。此外,低级ARID5B基因表达可能与MTX抗性相关联。

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