Tissue-resident microbiota impacts colorectal cancer progression and prognosis

To deepen the understanding of tissue-resident microbiota in colorectal cancer (CRC), we analyzed whole-genome and transcriptome data from 937 patients. We identified 249 genera and 361 species commonly present in both tumors and adjacent normal tissues (NATs). Distinct microbial signatures were associated with anatomical location, tumor stages, hypermutation status, mutations in CRC driver and DNA damage repair genes, as well as consensus molecular subtypes (CMSs). Notably, the presence of the pks island and elevated abundance of Enterobacteriaceae were linked to poor prognosis specifically in CMS2 tumors. Finally, microbial risk scores derived from taxa present in tumor or NATs predicted patient prognosis independently of established clinico-molecular factors. Prognostic taxa were strongly associated with tumor transcriptomic pathways related to hypoxia, immune response, and metabolic status. These findings revealed the heterogeneity of tissue-resident microbiota and their critical role in CRC progression, highlighting potential avenues for targeted intervention.

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Publication Details

Journal
Nature Communications
Published
2025-12-07
DOI
https://doi.org/10.1038/s41467-025-67047-2
Primary Topic
Gut microbiota and health
Type
article
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article

Tissue-resident microbiota impacts colorectal cancer progression and prognosis

Shida Zhu, Tian Luo, Tobias Sjöblom, Richard Palmqvist et al.
Nature Communications
Gut microbiota and health
article

Tissue-resident microbiota impacts colorectal cancer progression and prognosis

Shida Zhu, Tian Luo, Tobias Sjöblom, Richard Palmqvist, Anders Isaksson, Kui Wu, Ingrid Ljuslinder, Bengt Glimelius, Mathias Uhlén, Luís Nunes, Huahui Ren, Ting Zhu, Yiyi Zhong, Klara Hammarström, Meizhen Wu, Huanzi Zhong, Fuqiang Li, Zhun Shi, Cong Lin, Fangming Yang
article en

Abstract

To deepen the understanding of tissue-resident microbiota in colorectal cancer (CRC), we analyzed whole-genome and transcriptome data from 937 patients. We identified 249 genera and 361 species commonly present in both tumors and adjacent normal tissues (NATs). Distinct microbial signatures were associated with anatomical location, tumor stages, hypermutation status, mutations in CRC driver and DNA damage repair genes, as well as consensus molecular subtypes (CMSs). Notably, the presence of the pks island and elevated abundance of Enterobacteriaceae were linked to poor prognosis specifically in CMS2 tumors. Finally, microbial risk scores derived from taxa present in tumor or NATs predicted patient prognosis independently of established clinico-molecular factors. Prognostic taxa were strongly associated with tumor transcriptomic pathways related to hypoxia, immune response, and metabolic status. These findings revealed the heterogeneity of tissue-resident microbiota and their critical role in CRC progression, highlighting potential avenues for targeted intervention.

Nature CommunicationsVol. 17(1)
BGI Group (China) (CN), Uppsala University (SE), Oslo University Hospital (NO), Chinese Academy of Sciences (CN), Science for Life Laboratory (SE), Karolinska Institutet (SE), MD Precision (Canada) (CA), University of Chinese Academy of Sciences (CN), BGI Genomics, KTH Royal Institute of Technology (SE), Umeå University (SE)
Openalex Percentile: Top 64%
Gut microbiota and health
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