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Pooled analysis of 3,741 stool metagenomes from 18 cohorts for cross-stage and strain-level reproducible microbial biomarkers of colorectal cancer

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Author
Piccinno, Gianmarco
Thompson, Kelsey N.
Manghi, Paolo
Ghazi, Andrew R.
Thomas, Andrew Maltez
Blanco-Miguez, Aitor
Asnicar, Francesco
Mladenovic, Katarina
Pinto, Federica
Armanini, Federica
Puncochar, Michal
Piperni, Elisa
Heidrich, Vitor
Fackelmann, Gloria
Ferrero, Giulio
Tarallo, Sonia
Nguyen, Long H.
Yan, Yan
Keles, Nazim A.
Tuna, Bilge G.
Vymetálková, VeronikaORCiD Profile - 0000-0001-6870-6788WoS Profile - H-3167-2014Scopus Profile - 55964160100
Trompetto, Mario
Liška, VáclavORCiD Profile - 0000-0002-5226-0280WoS Profile - Q-4402-2017Scopus Profile - 8705914800
Hucl, Tomáš
Vodička, PavelORCiD Profile - 0000-0003-2376-1243WoS Profile - H-3370-2014Scopus Profile - 7004841464
Bencsikova, Beatrix
Carnogurska, Martina
Popovici, Vlad
Marmorino, Federica
Cremolini, Chiara
Pardini, Barbara
Cordero, Francesca
Song, Mingyang
Chan, Andrew T.
Derosa, Lisa
Zitvogel, Laurence
Huttenhower, Curtis
Naccarati, Alessio
Budinska, Eva
Segata, Nicola

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Publication date
2025
Published in
Nature Medicine
Volume / Issue
31 (7)
ISBN / ISSN
ISSN: 1078-8956
ISBN / ISSN
eISSN: 1546-170X
Funding Information
MSM//EH22_008/0004644
MSM//LX22NPO5102
FN//I-FNP-04
Metadata
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  • 1. Faculty of Medicine
  • Faculty of Medicine in Pilsen

This publication has a published version with DOI 10.1038/s41591-025-03693-9

Abstract
Associations between the gut microbiome and colorectal cancer (CRC) have been uncovered, but larger and more diverse studies are needed to assess their potential clinical use. We expanded upon 12 metagenomic datasets of patients with CRC (n = 930), adenomas (n = 210) and healthy control individuals (n = 976; total n = 2,116) with 6 new cohorts (n = 1,625) providing granular information on cancer stage and the anatomic location of tumors. We improved CRC prediction accuracy based solely on gut metagenomics (average area under the curve = 0.85) and highlighted the contribution of 19 newly profiled species and distinct Fusobacterium nucleatum clades. Specific gut species distinguish left-sided versus right-sided CRC (area under the curve = 0.66) with an enrichment of oral-typical microbes. We identified strain-specific CRC signatures with the commensal Ruminococcus bicirculans and Faecalibacterium prausnitzii showing subclades associated with late-stage CRC. Our analysis confirms that the microbiome can be a clinical target for CRC screening and characterizes it as a biomarker for CRC progression.
Keywords
Diagnostic markers, Metagenomics, Microbiome
Permanent link
https://hdl.handle.net/20.500.14178/3267
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WOS:001501019200001
SCOPUS:2-s2.0-105007151306
PUBMED:40461820
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Full text of this result is licensed under: Creative Commons Uveďte původ 4.0 International

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