Helicobacter pylori and interleukin-8 in gastric cancer

World J Gastroenterol. 2013 Dec 7;19(45):8192-202. doi: 10.3748/wjg.v19.i45.8192.

Abstract

Helicobacter pylori (H. pylori) is a major etiological factor in the development of gastric cancer. Large-scale epidemiological studies have confirmed the strong association between H. pylori infection and both cancer development and progression. Interleukin-8 (IL-8) is overexpressed in gastric mucosa exposed to H. pylori. The expression of IL-8 directly correlates with a poor prognosis in gastric cancer. IL-8 is multifunctional. In addition to its potent chemotactic activity, it can induce proliferation and migration of cancer cells. In this review, we focus on recent insights into the mechanisms of IL-8 signaling associated with gastric cancer. The relationship between IL-8 and H. pylori is discussed. We also summarize the current therapeutics against IL-8 in gastric cancer.

Keywords: Gastric cancer; Helicobacter pylori; Interleukin-8; Signals; Therapeutics.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / therapeutic use
  • Cell Transformation, Neoplastic / chemically induced
  • Cell Transformation, Neoplastic / immunology
  • Cell Transformation, Neoplastic / metabolism
  • Drug Design
  • Gastric Mucosa / immunology
  • Gastric Mucosa / metabolism*
  • Gastric Mucosa / microbiology*
  • Helicobacter Infections / epidemiology
  • Helicobacter Infections / immunology
  • Helicobacter Infections / metabolism*
  • Helicobacter Infections / microbiology*
  • Helicobacter pylori / immunology
  • Helicobacter pylori / pathogenicity*
  • Humans
  • Interleukin-8 / antagonists & inhibitors
  • Interleukin-8 / metabolism*
  • Molecular Targeted Therapy
  • Prognosis
  • Receptors, Interleukin-8 / antagonists & inhibitors
  • Receptors, Interleukin-8 / metabolism
  • Risk Factors
  • Signal Transduction
  • Stomach Neoplasms / immunology
  • Stomach Neoplasms / metabolism*
  • Stomach Neoplasms / microbiology*

Substances

  • Antineoplastic Agents
  • CXCL8 protein, human
  • Interleukin-8
  • Receptors, Interleukin-8