GDF15/GFRAL pathway as a metabolic signature for cachexia in patients with cancer

44Citations
Citations of this article
69Readers
Mendeley users who have this article in their library.

Abstract

Cachexia is a metabolic mutiny that directly reduces life expectancy in chronic conditions such as cancer. The underlying mechanisms associated with cachexia involve inflammation, metabolism, and anorexia. Therefore, the need to identify cachexia biomarkers is warranted to better understand catabolism change and assess various therapeutic interventions. Among inflammatory proteins, growth differentiation factor-15 (GDF15), an atypical transforming growth factor-beta (TGF-β) superfamily member, emerges as a stress-related hormone. In inflammatory conditions, cardiovascular diseases, and cancer, GDF15 is a biomarker for disease outcome. GDF15 is also implicated in energy homeostasis, body weight regulation, and plays a distinct role in cachexia. The recent discovery of its receptor, glial cell line-derived neurotrophic factor (GDNF) family receptor α-like (GFRAL), sheds light on its metabolic function. Herein, we critically review the mechanisms involving GDF15 in cancer cachexia and discuss therapeutic interventions to improve outcomes in people living with cancer.

Author supplied keywords

Cite

CITATION STYLE

APA

Ahmed, D. S., Isnard, S., Lin, J., Routy, B., & Routy, J. P. (2021, January 1). GDF15/GFRAL pathway as a metabolic signature for cachexia in patients with cancer. Journal of Cancer. Ivyspring International Publisher. https://doi.org/10.7150/jca.50376

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free