New models for cancer cachexia and their application to drug discovery
CC remains clinically challenging and requires improved translational research and therapeutic strategies. Improved preclinical models, such as personalized patient-derived xenograft models incorporating patient-specific immune profiles and microbiota, hold promise for precision medicine. Identification of standardized extracellular vesicle (EV) derived biomarkers and effective targeting of EV signaling pathways are critical research directions. In addition, clinical validation of appetite regulators such as glucagon-like peptide-1 and growth differentiation factor-15, along with comprehensive approaches integrating diet, exercise, and targeted pharmacological interventions, will be pivotal. Finally, multidisciplinary collaboration is essential to translate these findings into meaningful therapies that will ultimately improve patient prognosis and quality of life.
Authors
- Markus S. Anker (ORCID: https://orcid.org/0000-0002-4406-8555)
- Stephan von Haehling (ORCID: https://orcid.org/0000-0002-9818-042X)
- Ryosuke Sato (ORCID: https://orcid.org/0000-0003-0724-7842)
- Jochen Springer (ORCID: https://orcid.org/0000-0002-1225-0117)
Institutions
- Humboldt-Universität zu Berlin (DE)
- Universitätsmedizin Göttingen (DE)
- German Centre for Cardiovascular Research (DE)
- Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE)
- Deutsches Herzzentrum München (DE)
- Berlin Heart (Germany) (DE)
- University of Glasgow (GB)
Publication Details
- Journal
- Expert Opinion on Drug Discovery
- Published
- 2025-10-03
- DOI
- https://doi.org/10.1080/17460441.2025.2562020
- Primary Topic
- Vitamin C and Antioxidants Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00