Identification of 22 susceptibility loci associated with testicular germ cell tumors

  • John Pluta
  • Louise C Pyle
  • Kevin T Nead
  • Rona Wilf
  • Mingyao Li
  • Nandita Mitra
  • Benita Weathers
  • Kurt D'Andrea
  • Kristian Almstrup
  • Lynn Anson-Cartwright
  • Javier Benitez
  • Christopher D Brown
  • Stephen Chanock
  • Chu Chen
  • Victoria K Cortessis
  • Alberto Ferlin
  • Carlo Foresta
  • Marija Gamulin
  • Jourik A Gietema
  • Chiara Grasso
  • Mark H Greene
  • Tom Grotmol
  • Robert J Hamilton
  • Trine B Haugen
  • Russ Hauser
  • Michelle A T Hildebrandt
  • Matthew E Johnson
  • Robert Karlsson
  • Lambertus A Kiemeney
  • Davor Lessel
  • Ragnhild A Lothe
  • Jennifer T Loud
  • Chey Loveday
  • Paloma Martin-Gimeno
  • Coby Meijer
  • Jérémie Nsengimana
  • David I Quinn
  • Thorunn Rafnar
  • Shweta Ramdas
  • Lorenzo Richiardi
  • Rolf I Skotheim
  • Kari Stefansson
  • Clare Turnbull
  • David J Vaughn
  • Fredrik Wiklund
  • Xifeng Wu
  • Daphne Yang
  • Tongzhang Zheng
  • Andrew D Wells
  • Struan F A Grant
  • Ewa Rajpert-De Meyts
  • Stephen M Schwartz
  • D Timothy Bishop
  • Katherine A McGlynn
  • Peter A Kanetsky (Geteilte/r Letztautor/in)
  • Katherine L Nathanson (Geteilte/r Letztautor/in)
  • Testicular Cancer Consortium

Beteiligte Einrichtungen

Abstract

Testicular germ cell tumors (TGCT) are the most common tumor in young white men and have a high heritability. In this study, the international Testicular Cancer Consortium assemble 10,156 and 179,683 men with and without TGCT, respectively, for a genome-wide association study. This meta-analysis identifies 22 TGCT susceptibility loci, bringing the total to 78, which account for 44% of disease heritability. Men with a polygenic risk score (PRS) in the 95th percentile have a 6.8-fold increased risk of TGCT compared to men with median scores. Among men with independent TGCT risk factors such as cryptorchidism, the PRS may guide screening decisions with the goal of reducing treatment-related complications causing long-term morbidity in survivors. These findings emphasize the interconnected nature of two known pathways that promote TGCT susceptibility: male germ cell development within its somatic niche and regulation of chromosomal division and structure, and implicate an additional biological pathway, mRNA translation.

Bibliografische Daten

OriginalspracheEnglisch
ISSN2041-1723
DOIs
StatusVeröffentlicht - 23.07.2021
PubMed 34301922