Fig. 2
From: Nucleotide excision repair is a predictor of early relapse in pediatric acute lymphoblastic leukemia

Subgroups of Early and Late Relapsers compared at the time of diagnosis to relapse. (A) In early relapsers of the Staal dataset (n = 19) 12 genes were overexpressed at time of relapse (gray bars, P = .371) versus time of diagnosis (black bars). 2 genes were individually significant ERCC8 (P = .042) and ERCC6 (P = .019). (B) In early relapsers of the Hogan dataset (n = 27), 4 genes had an increased in gene expression. The pathway was significantly under-expressed (P = .007). No genes were significantly overexpressed. (C) In the combined early relapsers dataset (n = 46), 7 genes were upregulated at the time of recurrence (P = .180). (D) In the late relapsers of the Staal dataset (n = 8) 16 NER genes were upregulated at the time of relapse versus diagnosis (P = 0.007). 7 genes were individually significantly overexpressed, CCNH (P = .044), GTF2H4 (P = .049), RPA1 (P = .030), ERCC1 (P = .035), GTF2H2 (P = .033), RAD23B (P = .040), ERCC3 (P = .034). In the late relapsers of the Hogan dataset (n = 22), 16 genes were overexpressed (p = .007). 8 genes were individually significantly overexpressed, DDB1 (P = .003), ERCC2 (P = .021), ERCC1 (P = .015), DDB2 (P < .001), RPA2 (P = .005), RPA1 (P = .004), GTF2H3 (P < .001), and RPA3 (P < .001). (F) In the late relapsers of the combined dataset (n = 30), 16 genes were overexpressed at recurrence (P = .007) versus diagnosis. 11 genes showed significantly increased expression at relapse: ERCC5 (P = .035), GTF2H4 (P = .025), ERCC2 (P = .013), ERCC3 (P = .016), GTF2H2 (P = .012), DDB1 (P < .001), DDB2 (P < .001), ERCC1 (P < .001), RPA3 (P < .001), RPA2 (P < .001), and RPA1 (P < .001). * indicates P < .05 in a one tailed t-test