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Heart failure-induced microbial dysbiosis contributes to colonic tumour formation in mice

(2024) CARDIOVASCULAR RESEARCH. 120(6). p.612-622
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Abstract
Introduction Heart failure (HF) and cancer are the leading causes of death worldwide. Epidemiological studies revealed that HF patients are prone to develop cancer. Preclinical studies provided some insights into this connection, but the exact mechanisms remain elusive. In colorectal cancer (CRC), gut microbial dysbiosis is linked to cancer progression and recent studies have shown that HF patients display microbial dysbiosis.Aims This current study focussed on the effects of HF-induced microbial dysbiosis on colonic tumour formation.Methods and results C57BL/6J mice were subjected to myocardial infarction (MI), with sham surgery as control. After six weeks faeces were collected, processed for 16 s rRNA sequencing, and pooled for faecal microbiota transplantation. CRC tumour growth was provoked in germ-free mice by treating them with Azoxymethane/Dextran sodium sulphate. The CRC mice were transplanted with faeces from MI or sham mice. MI-induced HF resulted in microbial dysbiosis, characterized by a decreased alpha-diversity and microbial alterations on the genus level, several of which have been associated with CRC. We then performed faecal microbiota transplantation with faeces from HF mice in CRC mice, which resulted in a higher endoscopic disease score and an increase in the number of tumours in CRC mice.Conclusion We demonstrated that MI-induced HF contributes to colonic tumour formation by altering the gut microbiota composition, providing a mechanistic explanation for the observed association between HF and increased risk for cancer. Targeting the microbiome may present as a tool to mitigate HF-associated co-morbidities, especially cancer. Graphical abstract
Keywords
Tumour formation, Microbiome, Heart failure, Faecal microbiota transplantation, Cancer, GUT MICROBIOTA, FECAL MICROBIOTA, CANCER, SIGNATURE, GROWTH

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MLA
de Wit, Sanne, et al. “Heart Failure-Induced Microbial Dysbiosis Contributes to Colonic Tumour Formation in Mice.” CARDIOVASCULAR RESEARCH, vol. 120, no. 6, 2024, pp. 612–22, doi:10.1093/cvr/cvae038.
APA
de Wit, S., Geerlings, L., Shi, C., Dronkers, J., Schouten, E. M., Blancke, G., … de Boer, R. A. (2024). Heart failure-induced microbial dysbiosis contributes to colonic tumour formation in mice. CARDIOVASCULAR RESEARCH, 120(6), 612–622. https://doi.org/10.1093/cvr/cvae038
Chicago author-date
Wit, Sanne de, Lotte Geerlings, Canxia Shi, Just Dronkers, Elisabeth M. Schouten, Gillian Blancke, Vanessa Andries, et al. 2024. “Heart Failure-Induced Microbial Dysbiosis Contributes to Colonic Tumour Formation in Mice.” CARDIOVASCULAR RESEARCH 120 (6): 612–22. https://doi.org/10.1093/cvr/cvae038.
Chicago author-date (all authors)
de Wit, Sanne, Lotte Geerlings, Canxia Shi, Just Dronkers, Elisabeth M. Schouten, Gillian Blancke, Vanessa Andries, Tess Yntema, Wouter C. Meijers, Debby P. Y. Koonen, Lars Vereecke, Herman H. W. Sillje, Joseph-Pierre Aboumsallem, and Rudolf A. de Boer. 2024. “Heart Failure-Induced Microbial Dysbiosis Contributes to Colonic Tumour Formation in Mice.” CARDIOVASCULAR RESEARCH 120 (6): 612–622. doi:10.1093/cvr/cvae038.
Vancouver
1.
de Wit S, Geerlings L, Shi C, Dronkers J, Schouten EM, Blancke G, et al. Heart failure-induced microbial dysbiosis contributes to colonic tumour formation in mice. CARDIOVASCULAR RESEARCH. 2024;120(6):612–22.
IEEE
[1]
S. de Wit et al., “Heart failure-induced microbial dysbiosis contributes to colonic tumour formation in mice,” CARDIOVASCULAR RESEARCH, vol. 120, no. 6, pp. 612–622, 2024.
@article{01HV14H4YV3S9HHNVEWY311ZNQ,
  abstract     = {{Introduction Heart failure (HF) and cancer are the leading causes of death worldwide. Epidemiological studies revealed that HF patients are prone to develop cancer. Preclinical studies provided some insights into this connection, but the exact mechanisms remain elusive. In colorectal cancer (CRC), gut microbial dysbiosis is linked to cancer progression and recent studies have shown that HF patients display microbial dysbiosis.Aims This current study focussed on the effects of HF-induced microbial dysbiosis on colonic tumour formation.Methods and results C57BL/6J mice were subjected to myocardial infarction (MI), with sham surgery as control. After six weeks faeces were collected, processed for 16 s rRNA sequencing, and pooled for faecal microbiota transplantation. CRC tumour growth was provoked in germ-free mice by treating them with Azoxymethane/Dextran sodium sulphate. The CRC mice were transplanted with faeces from MI or sham mice. MI-induced HF resulted in microbial dysbiosis, characterized by a decreased alpha-diversity and microbial alterations on the genus level, several of which have been associated with CRC. We then performed faecal microbiota transplantation with faeces from HF mice in CRC mice, which resulted in a higher endoscopic disease score and an increase in the number of tumours in CRC mice.Conclusion We demonstrated that MI-induced HF contributes to colonic tumour formation by altering the gut microbiota composition, providing a mechanistic explanation for the observed association between HF and increased risk for cancer. Targeting the microbiome may present as a tool to mitigate HF-associated co-morbidities, especially cancer.

 Graphical abstract}},
  author       = {{de Wit, Sanne and  Geerlings, Lotte and  Shi, Canxia and  Dronkers, Just and  Schouten, Elisabeth M. and Blancke, Gillian and Andries, Vanessa and  Yntema, Tess and  Meijers, Wouter C. and  Koonen, Debby P. Y. and Vereecke, Lars and  Sillje, Herman H. W. and  Aboumsallem, Joseph-Pierre and  de Boer, Rudolf A.}},
  issn         = {{0008-6363}},
  journal      = {{CARDIOVASCULAR RESEARCH}},
  keywords     = {{Tumour formation,Microbiome,Heart failure,Faecal microbiota transplantation,Cancer,GUT MICROBIOTA,FECAL MICROBIOTA,CANCER,SIGNATURE,GROWTH}},
  language     = {{eng}},
  number       = {{6}},
  pages        = {{612--622}},
  title        = {{Heart failure-induced microbial dysbiosis contributes to colonic tumour formation in mice}},
  url          = {{http://doi.org/10.1093/cvr/cvae038}},
  volume       = {{120}},
  year         = {{2024}},
}

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