错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Genetic susceptibility of diffuse large B-cell lymphoma: a meta genome-wide association study in Asian population

  • Qian Cui,
  • Wen Tan,
  • Bao Song,
  • Rou-Jun Peng,
  • Ling Wang,
  • Rajkumar Dorajoo,
  • Kok Pin Ng,
  • Guo-Wang Lin,
  • Wing-Yan Au,
  • Raymond H. S. Liang,
  • Chiea Chuen Khor,
  • Qing-Ling Zhang,
  • Jia Nee FOO,
  • Sheng-Ping Li,
  • Fu-Ren Zhang,
  • Xue-Jun Zhang,
  • Xue-Qing Yu,
  • Qing Lan,
  • Stephen Chanock,
  • Wei-Hua Jia,
  • Soon Thye Lim,
  • Wen-Yu Li,
  • Nathaniel Rothman,
  • Jin-Xin Bei,
  • Jie Liu,
  • Dongxin Lin,
  • Jian-Jun Liu

摘要

Diffuse large B-cell lymphoma (DLBCL) is an aggressive malignancy and the most common form of non-Hodgkin lymphoma (NHL) that occurs worldwide. To discover risk factors and pathogenesis of DLBCL, we performed the largest GWAS of DLBCL to date in samples of East Asian ancestry, consisting of 2,888 patients with DLBCL and 12,458 controls. The meta-analysis identified three novel loci, rs2233434 on 6p21.1 (OR = 1.26, P = 1.17 × 10−8), rs11066015 on 12q24.12 (OR = 1.24, P = 6.57 × 10−9) and rs6032662 on 20q13.12 (OR = 1.24, P = 5.22 × 10−12). Fine mapping analysis revealed that the extensive association within the MHC region was driven by two novel HLA alleles, HLA-A*02 and HLA-DQB1*03. Functional annotation, eQTL and colocalization analyses of the susceptibility loci implicated NFKBIE/TCTE1, ALDH2/BRAP and CD40 as candidate disease genes. The pleiotropic effect analysis of the DLBCL loci revealed shared genetic susceptibility between DLBCL and several autoimmune diseases. Our study also suggested genetic heterogeneity between Asian and European populations by identifying ancestry-specific genetic associations. Overall, this study has implicated novel disease genes and molecular mechanism for DLBCL.