Association of relapse-linked ARID5B single nucleotide polymorphisms with drug resistance in B-cell precursor acute lymphoblastic leukemia cell lines.
ARID5B
B-cell precursor acute lymphoblastic leukemia
Drug sensitivities
Single nucleotide polymorphism
Journal
Cancer cell international
ISSN: 1475-2867
Titre abrégé: Cancer Cell Int
Pays: England
ID NLM: 101139795
Informations de publication
Date de publication:
04 Sep 2020
04 Sep 2020
Historique:
received:
12
05
2020
accepted:
29
08
2020
entrez:
27
1
2021
pubmed:
28
1
2021
medline:
28
1
2021
Statut:
epublish
Résumé
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. 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. 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). 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.
Sections du résumé
BACKGROUND
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
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
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
CONCLUSIONS
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.
Identifiants
pubmed: 33499894
doi: 10.1186/s12935-020-01524-0
pii: 10.1186/s12935-020-01524-0
pmc: PMC7839197
doi:
Types de publication
Journal Article
Langues
eng
Pagination
434Subventions
Organisme : Japan Society for the Promotion of Science
ID : 15K09645
Organisme : Japan Agency for Medical Research and Development
ID : JP17ck0106253h0001
Références
Nat Genet. 2009 Sep;41(9):1001-5
pubmed: 19684603
Clin Cancer Res. 2020 Jan 1;26(1):256-264
pubmed: 31573954
Cancer Med. 2019 Sep;8(11):5274-5288
pubmed: 31305009
Sci Rep. 2018 Jan 15;8(1):789
pubmed: 29335448
Nat Cell Biol. 2011 Jun;13(6):668-75
pubmed: 21532585
Nat Commun. 2013;4:2850
pubmed: 24276541
Nat Commun. 2019 Nov 25;10(1):5348
pubmed: 31767839
Nat Commun. 2018 Jan 18;9(1):286
pubmed: 29348612
Leukemia. 2010 Apr;24(4):894-6
pubmed: 20054350
Blood. 2010 Mar 4;115(9):1765-7
pubmed: 20042726
Blood. 2019 Feb 14;133(7):724-729
pubmed: 30510082
Nat Commun. 2018 Apr 9;9(1):1340
pubmed: 29632299
Blood. 2019 Oct 10;134(15):1227-1237
pubmed: 31350265
Hematol Oncol. 2020 Oct;38(4):614-617
pubmed: 32515032
Nat Genet. 2009 Sep;41(9):1006-10
pubmed: 19684604
PLoS One. 2017 Dec 13;12(12):e0188680
pubmed: 29236701
Nat Commun. 2016 Nov 08;7:13331
pubmed: 27824051
Nat Commun. 2017 Mar 03;8:14616
pubmed: 28256501
J Clin Oncol. 2012 Mar 1;30(7):751-7
pubmed: 22291082
Haematologica. 2019 Jan;104(1):128-137
pubmed: 30171027