4.8 Article

Germline Mutations in PALB2, BRCA1, and RAD51C, Which Regulate DNA Recombination Repair, in Patients With Gastric Cancer

Journal

GASTROENTEROLOGY
Volume 152, Issue 5, Pages 983-+

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.gastro.2016.12.010

Keywords

Stomach; Tumor; WES; Interaction

Funding

  1. No Stomach for Cancer Inc
  2. University of California, Davis
  3. Conicyt-Fondap [15130011]
  4. Investigacion Sanitaria/FEDER [14/00230, 14/00173]
  5. European Commission [635290]
  6. Fondo de Investigaciones, Universidad del Tolima [30113, 160120516, 450110, 160114]
  7. COLCIENCIAS [470115]
  8. El Consejo Nacional de Ciencia y Tecnologia-Fronteras de la Ciencia [clave 773]
  9. Instituto Mexicano del Seguro Social [FIS/IMSS/PROT/PRIO/13/027]
  10. Comite para el Desarrollo de la Investigacion, Universidad de Antioquia [CODI 2574]
  11. Intramural Research Program of the National Cancer Institute, National Institutes of Health, the Division of Cancer Epidemiology and Genetics
  12. V Foundation from Cancer Research
  13. National Cancer Institute of the National Institutes of Health [K12CA138464, R21CA199631]
  14. H2020 Societal Challenges Programme [635290] Funding Source: H2020 Societal Challenges Programme

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Up to 10% of cases of gastric cancer are familial, but so far, only mutations in CDH1 have been associated with gastric cancer risk. To identify genetic variants that affect risk for gastric cancer, we collected blood samples from 28 patients with hereditary diffuse gastric cancer (HDGC) not associated with mutations in CDH1 and performed whole-exome sequence analysis. We then analyzed sequences of candidate genes in 333 independent HDGC and non-HDGC cases. We identified 11 cases with mutations in PALB2, BRCA1, or RAD51C genes, which regulate homologous DNA recombination. We found these mutations in 2 of 31 patients with HDGC (6.5%) and 9 of 331 patients with sporadic gastric cancer (2.8%). Most of these mutations had been previously associated with other types of tumors and partially cosegregated with gastric cancer in our study. Tumors that developed in patients with these mutations had a mutation signature associated with somatic homologous recombination deficiency. Our findings indicate that defects in homologous recombination increase risk for gastric cancer.

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