Nature Communications (Apr 2017)

Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148

  • Jun Fang,
  • Jinping Jia,
  • Matthew Makowski,
  • Mai Xu,
  • Zhaoming Wang,
  • Tongwu Zhang,
  • Jason W. Hoskins,
  • Jiyeon Choi,
  • Younghun Han,
  • Mingfeng Zhang,
  • Janelle Thomas,
  • Michael Kovacs,
  • Irene Collins,
  • Marta Dzyadyk,
  • Abbey Thompson,
  • Maura O'Neill,
  • Sudipto Das,
  • Qi Lan,
  • Roelof Koster,
  • PanScan Consortium,
  • TRICL Consortium,
  • GenoMEL Consortium,
  • Rachael S. Stolzenberg-Solomon,
  • Peter Kraft,
  • Brian M. Wolpin,
  • Pascal W. T. C. Jansen,
  • Sara Olson,
  • Katherine A. McGlynn,
  • Peter A. Kanetsky,
  • Nilanjan Chatterjee,
  • Jennifer H. Barrett,
  • Alison M. Dunning,
  • John C. Taylor,
  • Julia A. Newton-Bishop,
  • D. Timothy Bishop,
  • Thorkell Andresson,
  • Gloria M. Petersen,
  • Christopher I. Amos,
  • Mark M. Iles,
  • Katherine L. Nathanson,
  • Maria Teresa Landi,
  • Michiel Vermeulen,
  • Kevin M. Brown,
  • Laufey T. Amundadottir

DOI
https://doi.org/10.1038/ncomms15034
Journal volume & issue
Vol. 8, no. 1
pp. 1 – 17

Abstract

Read online

Genetic variants at multiple loci of chr5p15.33 have been associated with susceptibility to numerous cancers. Here the authors show that the association of one of these loci may be explained by a variant, rs36115365, influencing telomerase reverse transcriptase (TERT) expression via ZNF148.