Abstract

BackgroundThe 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.MethodsWe 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.ResultsNo 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).ConclusionThese 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.

Highlights

  • 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)

  • We found that genotypes of the relapse-linked single nucleotide polymorphisms (SNPs) of ARID5B are associated with resistance to several chemotherapeutic agents

  • Genotype of susceptibility‐linked and relapse‐linked SNPs of ARID5B in BCP‐ALL cell lines We first analyzed ARID5B genotypes in 72 B-cell precursor-ALL (BCP-ALL) cell lines established from Japanese patients [16]

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Summary

Introduction

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). Recent genome-wide association studies (GWAS) on pediatric patients with BCP-ALL have identified common single nucleotide polymorphisms (SNPs) associated with disease susceptibility [1,2,3,4,5,6]. Further GWAS on pediatric ALL patients revealed that the other SNPs located in intron 2 of the ARID5B gene (i.e. rs4948488, rs2893881, and rs6479778; Fig. 1) were significantly associated with their relapse rate [14]. This clinical observation suggests that the genotype of these relapse-linked SNPs of ARID5B may be associated with the responses to chemotherapeutic agents. Few studies have focused on the association of ARID5B with drug sensitivities in BCP-ALL [15]

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