Role of folylpolyglutamate synthetase and folylpolyglutamate hydrolase in methotrexate accumulation and polyglutamylation in childhood leukemia

Inefficient polyglutamylation is a mechanism of resistance to methotrexate (MTX) in childhood T-lineage acute lymphoblastic leukemia (T-ALL) and in ac ute myeloid leukemia (AML) in comparison with childhood c/preB-ALL. We anal yzed the profile of MTX polyglutamylation in childhood c/preB-ALL, T-ALL, a nd AML(n = 45, 15, and 14, respectively), the activity of the MTX-polygluta mate synthesizing enzyme folylpolyglutamate synthetase (FPGS) (n = 39, 11, and 19, respectively) and of the MTX-polyglutamate breakdown enzyme folylpo lyglutamate hydrolase (FPGH) (n = 98, 25, and 34, respectively). MTX-Glu(4- 6) accumulation after 24 hours exposure to 1 mu mol/L [H-3]-MTX in vitro wa s lower in T-ALL (threefold) and AML (fourfold) compared with c/preB-ALL (P less than or equal to .001). The FPGS activity was twofold lower in T-ALL and AML than in c/preB-ALL samples (P < .01). FPGH activity was not differe nt between c/preB-ALL and T-ALL, but threefold higher in AML (P < .001). FP GS, FPGH, and the ratio FPGS/FPGH were correlated with MTX-Glu(4-6) accumul ation (r = .49, r = -.34 and r = .61, respectively). Multivariate analysis showed that FPGS, but not FPGH, was an independent contributor for MTX-Glu( 1-6) accumulation, but not for MTX-Glu(4-6) accumulation. In conclusion, lo w FPGS activity is associated with low accumulation of MTX-Glu(4-6) in T-AL L and AML. For the group of AML as compared with the group of ALL, a high F PGH activity can play an additional role. (C) 1999 by The American Society of Hematology.