Association between reduced folate carrier G80A polymorphism and methotrexate toxicity in childhood acute lymphoblastic leukemia: A meta-analysis

  • Hai Rong He
  • , Ping Liu
  • , Gong Hao He
  • , Wei Hua Dong
  • , Mao Yi Wang
  • , Ya Lin Dong
  • , Jun Lu

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Methotrexate (MTX) is a key component of chemotherapeutic regimens for childhood acute lymphoblastic leukemia (ALL), and enters the cell via active transport mediated by the reduced folate carrier (RFC1). A major single-nucleotide polymorphism of the RFC1 gene, G80A, which affects the activity of RFC1, may influence MTX toxicity in pediatric ALL. We collected all studies that investigated the association of RFC1 G80A polymorphism and MTX toxicity in pediatric ALL, and found inconsistency among their results. The aim of this meta-analysis was to summarize all of these studies in order to clarify the correlation between the RFC1 G80A polymorphism and MTX toxicity in pediatric ALL. A recessive model demonstrated no influence of the RFC1 G80A genotype on MTX toxicity. In conclusion, the RFC1 G80A polymorphism does not seem to be a good marker of MTX-related toxicity in pediatric ALL.

Original languageEnglish
Pages (from-to)2793-2800
Number of pages8
JournalLeukemia and Lymphoma
Volume55
Issue number12
DOIs
StatePublished - 1 Dec 2014

Keywords

  • Acute lymphoblastic leukemia
  • Methotrexate
  • Pharmacogenetics
  • Polymorphism
  • RFC1
  • Toxicity

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