Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing

Vogelaar, Ingrid P.; Post, Rachel S. van der; Krieken, J. Han J. M. van; Spruijt, Liesbeth; Zelst-Stams, Wendy A. G. van; Kets, C. Marleen; Lubinski, Jan; Jakubowska, Anna; Teodorczyk, Urszula; Aalfs, Cora M.; Hest, Liselotte P. van; Pinheiro, Hugo; Oliveira, Carla; Jhangiani, Shalini N.; Muzny, Donna M.; Gibbs, Richard A.; Lupski, James R.; Ligt, Joep de; Vissers, Lisenka E. L. M.; Hoischen, Alexander; Gilissen, Christian; Vorst, Maartje van de; Goeman, Jelle J.; Schackert, Hans K.; Ranzani, Guglielmina N.; Molinaro, Valeria; Garcia, Encarna B. Gomez; Hes, Frederik J.; Holinski-Feder, Elke; Genuardi, Maurizio; Ausems, Margreet G. E. M.; Sijmons, Rolf H.; Wagner, Anja; Kolk, Lizet E. van der; Björnevoll, Inga; Hoberg-Vetti, Hildegunn; Kessel, Ad Geurts van; Kuiper, Roland P.; Ligtenberg, Marjolijn J. L. und Hoogerbrugge, Nicoline (2017): Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing. In: European Journal of Human Genetics, Bd. 25, Nr. 11: S. 1246-1252

Abstract

Recognition of individuals with a genetic predisposition to gastric cancer (GC) enables preventive measures. However, the underlying cause of genetic susceptibility to gastric cancer remains largely unexplained. We performed germline whole-exome sequencing on leukocyte DNA of 54 patients from 53 families with genetically unexplained diffuse-type and intestinal-type GC to identify novel GC-predisposing candidate genes. As young age at diagnosis and familial clustering are hallmarks of genetic tumor susceptibility, we selected patients that were diagnosed below the age of 35, patients from families with two cases of GC at or below age 60 and patients from families with three GC cases at or below age 70. All included individuals were tested negative for germline CDH1 mutations before or during the study. Variants that were possibly deleterious according to in silico predictions were filtered using several independent approaches that were based on gene function and gene mutation burden in controls. Despite a rigorous search, no obvious candidate GC predisposition genes were identified. This negative result stresses the importance of future research studies in large, homogeneous cohorts.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Medizin
• Themengebiete: 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit
• ISSN: 1018-4813
• Sprache: Englisch