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Familial gastric cancer - aetiology and pathogenesis

  • Miriam Barber
  • , Rebecca C. Fitzgerald*
  • , Carlos Caldas
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

43 Scopus citations

Abstract

Gastric cancer is the second most common cause of cancer death worldwide. It is estimated that 5-10% of gastric cancer cases have a familial association; however, knowledge concerning the genetic predisposition to familial gastric cancer is currently limited. In this chapter we discuss what is known about the aetiology and pathogenesis of both the diffuse and intestinal forms of familial gastric cancer. We focus particularly on hereditary diffuse gastric cancer because the discovery of germ-line E-cadherin mutations in a number of affected families has opened the prospect of identifying gene carriers, with implications for clinical management. The interplay of other conventional risk factors, such as Helicobacter pylori infection, with genetic factors is also discussed. It is hoped that understanding the genetic basis for familial gastric cancer will facilitate the development of clinically useful screening and preventative procedures.

Original languageEnglish
Pages (from-to)721-734
Number of pages14
JournalBest Practice and Research: Clinical Gastroenterology
Volume20
Issue number4
DOIs
StatePublished - 2006
Externally publishedYes

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

Keywords

  • E-cadherin
  • Epstein-Barr virus
  • Helicobacter pylori
  • International Gastric Cancer Linkage Consortium
  • hereditary diffuse gastric cancer
  • intestinal familial gastric cancer

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