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Inflammasome: Cancer's friend or foe?

Journal

PHARMACOLOGY & THERAPEUTICS
Volume 143, Issue 1, Pages 24-33

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2014.02.002

Keywords

Inflammasome; Chronic inflammation; Carcinogenesis; Tumor progression; Tumor immunology

Funding

  1. Programma Operativo Regionale (POR) FSE Campania 'Model Organism' (MODO)
  2. Programma Operativo Regionale (POR) FSE Research in Experimental Medicine (CREME)

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High serum concentrations of IL-1 beta and IL-18 are correlated to malignancies with low-rate survival from the time of diagnosis. The multimeric complex of the inflammasome is responsible for IL-1 beta/IL-18 synthesis/release. A number of endogenous (damage-associated molecular patterns) and exogenous (pathogen-associated molecular patterns) stimuli can provide signals for inflammasome activation in cancer. These stimuli can behave as tumor promoters via inducing chronic inflammation that rather than providing a protective response to loss of tissue homeostasis, aberrantly facilitates tumor development. This view is contrasted in animal models of colon cancer in which the activation of some inflammasome complexes is associated with tumor protection. More studies are needed to understand the biology of the inflammasome in cancer and explore its therapeutic potential. (C) 2014 Elsevier Inc. All rights reserved.

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