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Polymorphisms of xenobiotic metabolizing enzymes and DNA repair genes and outcome in childhood acute lymphoblastic leukemia

✍ Scribed by Vanessa da Silva Silveira; Renata Canalle; Carlos Alberto Scrideli; Rosane Gomes de Paula Queiroz; Heloisa Bettiol; Elvis Terci Valera; Luiz Gonzaga Tone


Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
198 KB
Volume
33
Category
Article
ISSN
0145-2126

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✦ Synopsis


The interindividual variation in the activity of xenobiotic metabolizing enzymes and DNA repair genes could modify an individual's risk of recurrent malignancy and response to therapy. We investigated whether ALL outcome was related to polymorphisms in genes CYP2D6, MPO, EPHX1, NQO1, TS, XPD and XRCC1 in 95 consecutive ALL children by PCR or PCR-FRLP techniques. Polymorphisms in genes NQO1 and TS were associated with a significantly slow response to induction chemotherapy and NQO1 was also associated with a lower five-year event-free survival. This study suggests that polymorphisms of NQO1 and TS could be important for patient response to induction therapy and for treatment outcome.


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## Abstract Xenobiotic and folate metabolic pathways are important for the maintenance of genetic stability and may influence susceptibility to the development of childhood acute lymphoblastic leukaemia (ALL). In this study, we investigated 10 polymorphisms in 6 genes (__GSTM1__‐present/null, __GST