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In interaction with gender a common CYP3A4 polymorphism may influence the survival rate of chemotherapy for childhood acute lymphoblastic leukemia
- Source :
- Europe PubMed Central
- Publication Year :
- 2014
- Publisher :
- Springer Science and Business Media LLC, 2014.
-
Abstract
- CYP3A4 has an important role in the metabolisms of many drugs used in acute lymphoblastic leukemia (ALL) therapy; still, there are practically no publications about the role of CYP3A4 polymorphisms in ALL pharmacogenomics. We genotyped eight common single-nucleotide polymorphisms (SNPs) in the CYP3A4 and CYP3A5 genes in 511 children with ALL and investigated whether they influenced the survival of the patients. We involved additional 127 SNPs in 34 candidate genes and searched for interactions with respect to the survival rates. Significant association between the survival rates and the common rs2246709 SNP in the CYP3A4 gene was observed. The gender of the patients and the rs1076991 in the MTHFD1 gene strongly influenced this effect. We calculated new risk assessments involving the gender-rs2246709 interaction and showed that they significantly outperformed the earlier risk-group assessments at every time point. If this finding is confirmed in other populations, it can have a considerable prognostic significance.
- Subjects :
- Male
Oncology
medicine.medical_specialty
Candidate gene
Adolescent
Genotype
Single-nucleotide polymorphism
Biology
Polymorphism, Single Nucleotide
Minor Histocompatibility Antigens
Internal medicine
Genetics
medicine
Cytochrome P-450 CYP3A
Humans
SNP
Child
CYP3A5
Gene
Childhood Acute Lymphoblastic Leukemia
Survival rate
Retrospective Studies
Methylenetetrahydrofolate Dehydrogenase (NADP)
Pharmacology
Gender Identity
Infant
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Survival Rate
Child, Preschool
Pharmacogenomics
Immunology
Molecular Medicine
Female
Subjects
Details
- ISSN :
- 14731150 and 1470269X
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- The Pharmacogenomics Journal
- Accession number :
- edsair.doi.dedup.....c380434dc7f8cc60b6c8588f9cea0b57