Alternative splicing of the primary glucocorticoid receptor (GR) transcript, resulting in glucocorticoid receptor alpha GRα, glucocorticoid receptor beta GRP and glucocorticoid receptor gamma GRγ, may influence glucocorticoid (GC) resistance in childhood leukemia. To test this hypothesis, we determined GRα/β protein and GRα/β/γ mRNA expression levels in 43 initial acute lymphoblastic leukemia (iALL), 10 initial myeloid leukemia (iAML), 11 relapsed ALL (rALL) samples and one rAML sample. The results were correlated with in vitro GC resistance. GRa mRNA correlated with protein expression (ρ = 0.39-0.56, P < 0.05), but the protein to mRNA ratio was median 2.2-fold lower in rALL than in iALL (P < 0.05). GRβ mRNA was median 137-fold lower than GRα mRNA and correlated with GRα mRNA expression (ρ = 0.71, P < 0.0001). GRβ could not be detected at the protein level. GRγ accounted for a median of 2.8% (range 0.95-7.4%) of all GR transcripts. GRα (protein and mRNA) and GRβ (mRNA) expressions or GRα/GRβ ratios did not correlate with in vitro GC resistance in iALL, but GRγ (mRNA) did (ρ = 0.52, P = 0.007). These results suggest that GRβ is not involved in GC resistance in childhood leukemia. The association between GRγ expression and in vitro GC resistance in iALL and the decreased protein/mRNA ratio in rALL, a subgroup resistant to GCs, warrants further exploration.

, , ,,
Department of Pediatrics