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Detection of Fusobacterium nucleatum in Patients with Colitis-Associated Colorectal Cancer

Fusobacterium nucleatum is supposed to play a critical role in the development of colorectal cancer. The species has also been associated with ulcerative colitis (UC) that can progress into colorectal cancer, however, the involvement of bacteria in this process remains unclear. We analysed 177 colon...

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Autores principales: Dregelies, Theresa, Haumaier, Franziska, Sterlacci, William, Backert, Steffen, Vieth, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356651/
https://www.ncbi.nlm.nih.gov/pubmed/37468740
http://dx.doi.org/10.1007/s00284-023-03398-7
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author Dregelies, Theresa
Haumaier, Franziska
Sterlacci, William
Backert, Steffen
Vieth, Michael
author_facet Dregelies, Theresa
Haumaier, Franziska
Sterlacci, William
Backert, Steffen
Vieth, Michael
author_sort Dregelies, Theresa
collection PubMed
description Fusobacterium nucleatum is supposed to play a critical role in the development of colorectal cancer. The species has also been associated with ulcerative colitis (UC) that can progress into colorectal cancer, however, the involvement of bacteria in this process remains unclear. We analysed 177 colon biopsies obtained from patients during screening, including 20 healthy controls, 56 UC cases and 69 cases at different stages of progression to colitis-associated cancer (CAC); 32 samples of sporadic colorectal carcinoma (sCRC) were also included. The presence of F. nucleatum was detected by quantitative real-time PCR (qPCR). Our data show an association between the presence of the bacteria and the progression of carcinogenesis in UC patients. In 39.5% of CAC samples F. nucleatum was detected, compared to only 1.8% in UC cases. The bacteria were detected in 6.3% of samples with initial neoplastic transformation, so-called low-grade dysplasia (LGD), whereas high-grade dysplasia (HGD) resulted in 33.3% of samples positive for F. nucleatum. The fraction of F. nucleatum-positive samples from sCRC cases was 56.3%, which was not significantly different to the CAC group. We conclude that F. nucleatum is associated with the occurrence and progression of colon carcinogenesis, rather than with UC itself. SUPPLEMENTARY INFORMATION: The online version of this article contains supplementary material available 10.1007/s00284-023-03398-7.
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spelling pubmed-103566512023-07-21 Detection of Fusobacterium nucleatum in Patients with Colitis-Associated Colorectal Cancer Dregelies, Theresa Haumaier, Franziska Sterlacci, William Backert, Steffen Vieth, Michael Curr Microbiol Article Fusobacterium nucleatum is supposed to play a critical role in the development of colorectal cancer. The species has also been associated with ulcerative colitis (UC) that can progress into colorectal cancer, however, the involvement of bacteria in this process remains unclear. We analysed 177 colon biopsies obtained from patients during screening, including 20 healthy controls, 56 UC cases and 69 cases at different stages of progression to colitis-associated cancer (CAC); 32 samples of sporadic colorectal carcinoma (sCRC) were also included. The presence of F. nucleatum was detected by quantitative real-time PCR (qPCR). Our data show an association between the presence of the bacteria and the progression of carcinogenesis in UC patients. In 39.5% of CAC samples F. nucleatum was detected, compared to only 1.8% in UC cases. The bacteria were detected in 6.3% of samples with initial neoplastic transformation, so-called low-grade dysplasia (LGD), whereas high-grade dysplasia (HGD) resulted in 33.3% of samples positive for F. nucleatum. The fraction of F. nucleatum-positive samples from sCRC cases was 56.3%, which was not significantly different to the CAC group. We conclude that F. nucleatum is associated with the occurrence and progression of colon carcinogenesis, rather than with UC itself. SUPPLEMENTARY INFORMATION: The online version of this article contains supplementary material available 10.1007/s00284-023-03398-7. Springer US 2023-07-19 2023 /pmc/articles/PMC10356651/ /pubmed/37468740 http://dx.doi.org/10.1007/s00284-023-03398-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Dregelies, Theresa
Haumaier, Franziska
Sterlacci, William
Backert, Steffen
Vieth, Michael
Detection of Fusobacterium nucleatum in Patients with Colitis-Associated Colorectal Cancer
title Detection of Fusobacterium nucleatum in Patients with Colitis-Associated Colorectal Cancer
title_full Detection of Fusobacterium nucleatum in Patients with Colitis-Associated Colorectal Cancer
title_fullStr Detection of Fusobacterium nucleatum in Patients with Colitis-Associated Colorectal Cancer
title_full_unstemmed Detection of Fusobacterium nucleatum in Patients with Colitis-Associated Colorectal Cancer
title_short Detection of Fusobacterium nucleatum in Patients with Colitis-Associated Colorectal Cancer
title_sort detection of fusobacterium nucleatum in patients with colitis-associated colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356651/
https://www.ncbi.nlm.nih.gov/pubmed/37468740
http://dx.doi.org/10.1007/s00284-023-03398-7
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