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Updated: Aug 11, 2026

The Colon-26 Carcinoma Tumor-bearing Mouse as a Model for the Study of Cancer Cachexia
Published on: November 30, 2016
Novel Antibodies for Managing Cachexia
Cameron Oswalt1,2, Jeffrey Crawford1,2
11Division of Medical Oncology, Department of Medicine, Duke University Health System, Durham, North Carolina, USA; email: cameron.oswalt@duke.edu, jeffrey.a.crawford@duke.edu.
Cachexia, a syndrome of weight loss and muscle wasting, is mediated by the GDF-15/GFRAL pathway. Inhibiting this pathway with therapies like ponsegromab shows promise for treating cachexia symptoms.
Area of Science:
- Biomedical research
- Translational medicine
- Oncology
Background:
- Cachexia is a complex syndrome causing weight loss and muscle wasting, often linked to chronic diseases like cancer.
- Current cachexia treatments are limited, necessitating novel therapeutic strategies.
- The Growth Differentiation Factor 15 (GDF-15)-Glial cell-derived neurotrophic factor family receptor alpha-like (GFRAL) signaling pathway is a key mediator of cachexia.
Purpose of the Study:
- To investigate the therapeutic potential of targeting the GDF-15/GFRAL pathway for cachexia.
- To evaluate the efficacy of ponsegromab, a GDF-15 inhibitor, in managing cachexia-related symptoms.
Main Methods:
- Clinical investigation of ponsegromab, a monoclonal antibody targeting GDF-15.
- Assessment of body weight changes and other cachexia symptoms in patients with cancer.
Main Results:
- Ponsegromab treatment demonstrated improvements in body weight and other cachexia symptoms in cancer patients.
- The GDF-15/GFRAL axis inhibition emerged as a promising therapeutic avenue for cachexia.
- Development of anti-GDF-15 and anti-GFRAL therapies is ongoing.
Conclusions:
- Targeting the GDF-15/GFRAL pathway represents a significant advancement in cachexia treatment.
- Further research and clear trial endpoints are crucial for developing effective cachexia therapies.
- The systemic impact of cachexia and potential therapeutic applications are broad.
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