Evidence map›Paper›PMID 41354681›Full record

ArticleNature communications2025

Tissue-resident microbiota impacts colorectal cancer progression and prognosis.

Zhun Shi, Huahui Ren, Cong Lin, Fuqiang Li, Meizhen Wu, Fangming Yang, Tian Luo, Luís Nunes, Anders Isaksson, Klara Hammarström and 10 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
  2. Review
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  9. Article
  10. Programming the tumor microenvironment through microbiome-driven mechanisms.Frontiers in cellular and infection microbiology · 2026
    Review
  11. Review
  12. Review
  13. Article
  14. IntratumoralFrontiers in immunology · 2026
    Article
  15. Article
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Zhun Shi *BGI Genomics, Shenzhen, China.ORCID http://orcid.org/0000-0001-9270-8177
Huahui Ren *BGI Genomics, Shenzhen, China.ORCID http://orcid.org/0000-0003-1154-9448
Cong Lin *HIM-BGI Omics Center, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, BGI Research, Hangzhou, China. lincong@genomics.cn.ORCID http://orcid.org/0009-0002-1494-4427
Fuqiang Li *HIM-BGI Omics Center, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, BGI Research, Hangzhou, China.ORCID http://orcid.org/0000-0002-2085-1457
Meizhen WuBGI Genomics, Shenzhen, China.ORCID http://orcid.org/0009-0001-7702-0080
Fangming YangBGI Genomics, Shenzhen, China.
Tian LuoBGI Genomics, Shenzhen, China.
Luís NunesDepartment of Molecular Oncology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0002-3391-1607
Anders IsakssonScience for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Klara HammarströmScience for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Ting ZhuCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.
Shida ZhuBGI Genomics, Shenzhen, China.
Yiyi ZhongBGI Genomics, Shenzhen, China.
Ingrid LjuslinderDepartment of Radiation Sciences, Oncology, Umeå University, Umeå, Sweden.
Mathias UhlénScience for Life Laboratory, Department of Protein Science, KTH-Royal Institute of Technology, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-4858-8056
Richard PalmqvistDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.ORCID http://orcid.org/0000-0002-9933-2843
Bengt GlimeliusScience for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-5440-791X
Kui WuBGI Genomics, Shenzhen, China. wukui@genomcis.cn.ORCID http://orcid.org/0000-0002-6857-7231
Tobias SjöblomScience for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden. tobias.sjoblom@igp.uu.se.ORCID http://orcid.org/0000-0001-6668-4140
Huanzi ZhongBGI Genomics, Shenzhen, China. zhonghuanzi@genomics.cn.ORCID http://orcid.org/0000-0001-9512-1750

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Colorectal NeoplasmsGastrointestinal MicrobiomeMicrobiotaAgedDisease ProgressionFemaleHumansMaleMiddle AgedMutationPrognosisTranscriptome

Identifiers

PMID41354681
PMCPMC12789584

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.