Fusobacterium nucleatum Abundance is Associated with Cachexia in Colorectal Cancer Patients: The ColoCare Study
- PMID: 39587707
- PMCID: PMC11588854
- DOI: 10.1002/cam4.70431
Fusobacterium nucleatum Abundance is Associated with Cachexia in Colorectal Cancer Patients: The ColoCare Study
Abstract
Background: Cachexia accounts for about 20% of all cancer-related deaths and indicates poor prognosis. The impact of Fusobacterium nucleatum (Fn), a microbial risk factor for colorectal cancer (CRC), on the development of cachexia in CRC has not been established.
Methods: We evaluated the association between Fn abundance in pre-surgical stool samples and onset of cachexia at 6 months post-surgery in n = 87 patients with stages I-III CRC in the ColoCare Study.
Results: High fecal Fn abundance compared to negative/low fecal Fn abundance was associated with 4-fold increased risk of cachexia onset at 6 months post-surgery (OR = 4.82, 95% CI = 1.15, 20.10, p = 0.03).
Conclusion: Our findings suggest that high fecal Fn abundance was associated with an increased risk of cachexia at 6 months post-surgery in CRC patients. This is the first study to link Fn abundance with cachexia in CRC patients, offering novel insights into biological mechanisms and potential management of cancer cachexia. Due to the small sample size, our results should be interpreted with caution. Future studies with larger sample sizes are needed to validate these findings.
Keywords: Fusobacterium nucleatum; cachexia; colorectal cancer.
© 2024 The Author(s). Cancer Medicine published by John Wiley & Sons Ltd.
Conflict of interest statement
C.M.U. has as cancer center director oversight over research funded by several pharmaceutical companies, but has not received funding directly herself. The remaining authors declare no conflict of interest.
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References
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- LeBlanc T. W., Nipp R. D., Rushing C. N., et al., “Correlation Between the International Consensus Definition of the Cancer Anorexia‐Cachexia Syndrome (CACS) and Patient‐Centered Outcomes in Advanced Non‐small Cell Lung Cancer,” Journal of Pain and Symptom Management 49, no. 4 (2015): 680–689, 10.1016/j.jpainsymman.2014.09.008. - DOI - PubMed
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- R01 CA207371/CA/NCI NIH HHS/United States
- German Cancer Research Center
- R01 CA254108/CA/NCI NIH HHS/United States
- the Rahel-Goitein-Straus-Program, Medical Faculty Heidelberg University
- Huntsman Cancer Foundation
- R01 CA189184/CA/NCI NIH HHS/United States
- R01 AG083580/AG/NIA NIH HHS/United States
- ERA-NET (European Research Area Network) on Translational Cancer Research (TRANSCAN) project
- U01 CA206110/CA/NCI NIH HHS/United States
- the German Ministry of Education and Research project PerMiCCion (01KD2101D)
- Stiftung LebensBlicke, Matthias Lackas Stiftung, Claussen-Simon Stiftung
- K07 CA222060/CA/NCI NIH HHS/United States
- the German Consortium of Translational Cancer Research, (DKTK)
- R01 CA211705/CA/NCI NIH HHS/United States
- University of Utah Immunology, Inflammation, and Infectious Disease Initiative
- Cancer Control and Population Health Sciences (CCPS) at the University of Utah
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