1. ¹Centre de Recherche, Hôpital Sainte-Justine, Centre Hospitalier Universitaire Mère-Enfant, Montréal, Québec, Canada
2. ²Département de Pédiatrie, Université de Montréal, Montréal, Québec, Canada
3. ³Département de Pharmacologie, Université de Montréal, Montréal, Québec, Canada

Correspondence: Dr M Krajinovic, Centre de recherche, Hôpital Sainte-Justine, 3175 Côte Ste-Catherine, Montréal, Québec, Canada H3T 1C5. Tel: +1 514 345 4931 ext. 6259; Fax: +1 514 345 4731; E-mail: maja.krajinovic@umontreal.ca

Received 11 February 2005; Revised 11 May 2005; Accepted 19 July 2005; Published online 30 August 2005.

Abstract

Thymidylate synthase (TS) is an essential enzyme in proliferating cells and an important target for several chemotherapeutics. Several TS gene polymorphisms correlate with variable TS expression: a double (2R) and triple (3R) 28-bp repeat element, a G to C substitution of the 3R allele and a 6 bp variation in 3'UTR. We have previously shown that childhood acute lymphoblastic leukemia (ALL) patients who are homozygous for the 3R allele had reduced event-free survival (EFS) probabilities. Here, we analyzed all three polymorphisms in an extended group of ALL patients (n=259). The effect of the 3R homozygosity on ALL outcome was confirmed (P=0.006), whereas 6 bp polymorphism did not influence EFS when analyzed separately. No significant difference among 3R3R genotype subgroups, as defined by a G to C substitution, was observed. The haplotype analysis revealed the higher frequency of the 3RC/6 bp+ haplotype (P=0.04) and the protective role of the 2R/6b p- (P=0.04). Consequently, homozygosity for the 6 bp- allele appeared to reduce an event-predisposing effect of 3R variant. Although of importance for translation into the clinical practice, these findings need confirmation in larger studies.