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Somatic copy number alterations in gastric adenocarcinomas among Asian and Western patients

  • Steven E. Schumacher
  • , Byoung Yong Shim
  • , Giovanni Corso
  • , Min Hee Ryu
  • , Yoon Koo Kang
  • , Franco Roviello
  • , Gordon Saksena
  • , Shouyong Peng
  • , Ramesh A. Shivdasani
  • , Adam J. Bass
  • , Rameen Beroukhim
  • Dana-Farber Cancer Institute
  • Broad Institute
  • Azienda Ospedaliera Universitaria Senese
  • University of Ulsan
  • Brigham and Women’s Hospital

Research output: Contribution to journal › Article › peer-review

28 Scopus citations

Abstract

Gastric cancer, a leading worldwide cause of cancer mortality, shows high geographic and ethnic variation in incidence rates, which are highest in East Asia. The anatomic locations and clinical behavior also differ by geography, leading to the controversial idea that Eastern and Western forms of the disease are distinct. In view of these differences, we investigated whether gastric cancers from Eastern and Western patients show distinct genomic profiles. We used high-density profiling of somatic copy-number aberrations to analyze the largest collection to date of gastric adenocarcinomas and utilized genotyping data to rigorously annotate ethnic status. The size of this collection allowed us to accurately identify regions of significant copy-number alteration and separately to evaluate tumors arising in Eastern and Western patients. Among molecular subtypes classified by The Cancer Genome Atlas, the frequency of gastric cancers showing chromosomal instability was modestly higher in Western patients. After accounting for this difference, however, gastric cancers arising in Easterners and Westerners have highly similar somatic copy-number patterns. Only one genomic event, focal deletion of the phosphatase gene PTPRD, was significantly enriched in Western cases, though also detected in Eastern cases. Thus, despite the different risk factors and clinical features, gastric cancer appears to be a fundamentally similar disease in both populations and the divergent clinical outcomes cannot be ascribed to different underlying structural somatic genetic aberrations.

Original languageEnglish
Article numbere0176045
JournalPLoS ONE
Volume12
Issue number4
DOIs
StatePublished - Apr 2017

Bibliographical note

Publisher Copyright:
© 2017 Schumacher et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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