GDF15 neutralization restores muscle function and physical performance in a mouse model of cancer cachexia

Ja Young Kim-Muller(Pfizer (United States)), LouJin Song(Pfizer (United States)), Brianna LaCarubba Paulhus(Pfizer (United States)), Evanthia Pashos(Pfizer (United States)), Xiangping Li(Pfizer (United States)), Anthony Rinaldi(Pfizer (United States)), Stephanie Joaquim(Pfizer (United States)), John C. Stansfield(Pfizer (United States)), Jiangwei Zhang(Pfizer (United States)), Andrew Robertson(Pfizer (United States)), Jincheng Pang(Pfizer (United States)), Alan Opsahl(Pfizer (United States)), Magalie Boucher(Pfizer (United States)), Danna M. Breen(Pfizer (United States)), Katherine Hales(Pfizer (United States)), Abdul Q. Sheikh(Pfizer (United States)), Zhidan Wu(Pfizer (United States)), Bei B. Zhang(Pfizer (United States))
Cell Reports
January 1, 2023
Cited by 92Open Access
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Abstract

Cancer cachexia is a disorder characterized by involuntary weight loss and impaired physical performance. Decline in physical performance of patients with cachexia is associated with poor quality of life, and currently there are no effective pharmacological interventions that restore physical performance. Here we examine the effect of GDF15 neutralization in a mouse model of cancer-induced cachexia (TOV21G) that manifests weight loss and muscle function impairments. With comprehensive assessments, our results demonstrate that cachectic mice treated with the anti-GDF15 antibody mAB2 exhibit body weight gain with near-complete restoration of muscle mass and markedly improved muscle function and physical performance. Mechanistically, the improvements induced by GDF15 neutralization are primarily attributed to increased caloric intake, while altered gene expression in cachectic muscles is restored in caloric-intake-dependent and -independent manners. The findings indicate potential of GDF15 neutralization as an effective therapy to enhance physical performance of patients with cachexia.


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