Novel susceptibility variants at the ERG locus for childhood acute lymphoblastic leukemia in Hispanics.

Published

Journal Article

Acute lymphoblastic leukemia (ALL) is the most common malignancy in children. Characterized by high levels of Native American ancestry, Hispanics are disproportionally affected by this cancer with high incidence and inferior survival. However, the genetic basis for this disparity remains poorly understood because of a paucity of genome-wide investigation of ALL in Hispanics. Performing a genome-wide association study (GWAS) in 940 Hispanic children with ALL and 681 ancestry-matched non-ALL controls, we identified a novel susceptibility locus in the ERG gene (rs2836365; P = 3.76 × 10-8; odds ratio [OR] = 1.56), with independent validation (P = .01; OR = 1.43). Imputation analyses pointed to a single causal variant driving the association signal at this locus overlapping with putative regulatory DNA elements. The effect size of the ERG risk variant rose with increasing Native American genetic ancestry. The ERG risk genotype was underrepresented in ALL with the ETV6-RUNX1 fusion (P < .0005) but enriched in the TCF3-PBX1 subtype (P < .05). Interestingly, ALL cases with germline ERG risk alleles were significantly less likely to have somatic ERG deletion (P < .05). Our results provide novel insights into genetic predisposition to ALL and its contribution to racial disparity in this cancer.

Full Text

Duke Authors

Cited Authors

  • Qian, M; Xu, H; Perez-Andreu, V; Roberts, KG; Zhang, H; Yang, W; Zhang, S; Zhao, X; Smith, C; Devidas, M; Gastier-Foster, JM; Raetz, E; Larsen, E; Burchard, EG; Winick, N; Bowman, WP; Martin, PL; Borowitz, M; Wood, B; Antillon-Klussmann, F; Pui, C-H; Mullighan, CG; Evans, WE; Hunger, SP; Relling, MV; Loh, ML; Yang, JJ

Published Date

  • February 14, 2019

Published In

Volume / Issue

  • 133 / 7

Start / End Page

  • 724 - 729

PubMed ID

  • 30510082

Pubmed Central ID

  • 30510082

Electronic International Standard Serial Number (EISSN)

  • 1528-0020

Digital Object Identifier (DOI)

  • 10.1182/blood-2018-07-862946

Language

  • eng

Conference Location

  • United States