Involvement of miRNA polymorphism in mucositis development in childhood acute lymphoblastic leukemia treatment

被引:11
作者
Gutierrez-Camino, Angela [1 ,2 ]
Umerez, Maitane [1 ]
Lopez-Lopez, Elixabet [1 ,2 ]
Santos-Zorrozua, Borja [1 ]
Martin-Guerrero, Idoia [1 ,2 ]
Garcia de Andoin, Nagore [3 ,4 ]
Ana, Sastre [5 ]
Navajas, Aurora [2 ,6 ]
Astigarraga, Itziar [2 ,4 ,6 ]
Garcia-Orad, Africa [1 ,2 ]
机构
[1] Univ Basque Country, Dept Genet Phys Anthropol & Anim Physiol, UPV EHU, Leioa 48940, Spain
[2] BioCruces Hlth Res Inst, Baracaldo 48903, Spain
[3] Univ Hosp Donostia, Dept Pediat, San Sebastian 20014, Spain
[4] Univ Basque Country, Dept Pediat, UPV EHU, Leioa 48940, Spain
[5] Univ Hosp La Paz, Dept Oncohematol, Madrid 28046, Spain
[6] Univ Hosp Cruces, Dept Pediat, Baracaldo 48903, Spain
关键词
acute lymphoblastic leukemia; chemotherapy; miRNA; mucositis; SNP; PRIMARY MICRORNAS; ORAL MUCOSITIS; GENES; EXPRESSION; IDENTIFICATION; PERSPECTIVES; BIOMARKERS; PHENOTYPE; TOXICITY; DATABASE;
D O I
10.2217/pgs-2018-0113
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim: Mucositis, linked to methotrexate, daunorubicin or cyclophosphamide, is a frequent childhood acute lymphoblastic leukemia (ALL) therapy side effect. miRNAs regulate the expression of pharmacokinetic/pharmacodynamic pathway genes. SNPs in miRNAs could affect their levels or function, and affect their pharmacokinetic/pharmacodynamic pathway target genes. Our aim was to determine the association between miRNA genetic variants targeting mucositis-related genes and mucositis-developing risk. Patients & methods: We analyzed 160 SNPs in 179 Spanish children with B-cell precursor ALL homogeneously treated with LAL/SHOP protocols. Results: We identified three SNPs in miR-4268, miR-4751 and miR-3117 associated with mucositis, diarrhea and vomiting, respectively. Conclusion: The effect of these SNPs on genes related to drug pharmacokinetics/pharmacodynamics could explain mucositis, diarrhea and vomiting development during ALL therapy.
引用
收藏
页码:1403 / 1412
页数:10
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