The Emerging Role of Interleukin 1β (IL-1β) in Cancer Cachexia.
Barry J A LairdDonald McMillanRichard J E SkipworthMarie T FallonD Robert PavalIain McNeishIain J GallagherPublished in: Inflammation (2021)
Treatment of cancer cachexia remains an unmet need. The host-tumour interface and the resulting sequestration of the pro-inflammatory cytokine Il-1β is critical in cachexia development. Neuroinflammation mediated via IL-1β through the hypothalamic pituitary axis results in increased muscle proteolysis and adipose lipolysis, thus creating a prolonged stress-like environment with loss of appetite and increased resting energy expenditure. Recent trials using a monoclonal antibody targeting IL-1β, canakinumab, have shown a potential role in lung cancer; however, a potential role of targeting IL-1β to treat cachexia in patients with lung cancer is unclear, yet the underlying pathophysiology provides a sound rationale that this may be a viable therapeutic approach.
Keyphrases
- papillary thyroid
- monoclonal antibody
- adipose tissue
- clinical trial
- traumatic brain injury
- skeletal muscle
- type diabetes
- insulin resistance
- metabolic syndrome
- drug delivery
- young adults
- blood pressure
- heart rate variability
- lymph node metastasis
- risk assessment
- lipopolysaccharide induced
- stress induced
- human health
- heat stress
- smoking cessation