By the same authors

From the same journal

From the same journal

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A

Research output: Contribution to journalArticle

Author(s)

  • Jayaram Vijayakrishnan
  • Marc Henrion
  • Anthony V Moorman
  • Bettina Fiege
  • Rajiv Kumar
  • Miguel Inacio da Silva Filho
  • Amy Holroyd
  • Rolf Koehler
  • Hauke Thomsen
  • Julie A Irving
  • James M Allan
  • Sally E Kinsey
  • Eamonn Sheridan
  • Pamela D Thompson
  • Per Hoffmann
  • Markus M Nöthen
  • Thomas W Mühleisen
  • Lewin Eisele
  • Claus R Bartram
  • Martin Schrappe
  • Mel Greaves
  • Kari Hemminki
  • Christine J Harrison
  • Martin Stanulla
  • Richard S Houlston

Department/unit(s)

Publication details

JournalScientific Reports
DatePublished - 14 Oct 2015
Issue number15065
Volume5
Number of pages8
Pages (from-to)1-8
Original languageEnglish

Abstract

Genome-wide association studies (GWAS) have provided strong evidence for inherited predisposition to childhood acute lymphoblastic leukaemia (ALL) identifying a number of risk loci. We have previously shown common SNPs at 9p21.3 influence ALL risk. These SNP associations are generally not themselves candidates for causality, but simply act as markers for functional variants. By means of imputation of GWAS data and subsequent validation SNP genotyping totalling 2,177 ALL cases and 8,240 controls, we have shown that the 9p21.3 association can be ascribed to the rare high-impact CDKN2A p.Ala148Thr variant (rs3731249; Odds ratio = 2.42, P = 3.45 × 10(-19)). The association between rs3731249 genotype and risk was not specific to particular subtype of B-cell ALL. The rs3731249 variant is associated with predominant nuclear localisation of the CDKN2A transcript suggesting the functional effect of p.Ala148Thr on ALL risk may be through compromised ability to inhibit cyclin D within the cytoplasm.

Discover related content

Find related publications, people, projects, datasets and more using interactive charts.

View graph of relations