Evidence map›Paper›PMID 36765047›Full record

ArticleNature communications2023

Bile salt hydrolase in non-enterotoxigenic Bacteroides potentiates colorectal cancer.

Lulu Sun, Yi Zhang, Jie Cai, Bipin Rimal, Edson R Rocha, James P Coleman, Chenran Zhang, Robert G Nichols, Yuhong Luo, Bora Kim and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 3 pooled it
24.6field-weighted citation impact, top 1% of its field
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

87 citing papers in PubMed, 3 syntheses or guidelines pooled it, 107 citations in OpenAlex.

  1. Pooled it
  2. Systematic review: The gut microbiota as a link between colorectal cancer and obesity.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Pooled it
  3. Pooled it
  4. Review
  5. Novel bacteriumGut microbes · 2026
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. NontoxigenicMicroorganisms · 2026
    Review
  12. Article
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  15. Article
  16. Article
  17. Review
  18. Gut Microbiota-Driven Pathways Linking Chronic Stress to Tumor Progression.International journal of biological sciences · 2026
    Review
  19. Review
  20. Article

27 more citing papers are in PubMed but not listed here.

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

17 authors at 4 institutions in 2 countries.

Lulu Sun *Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.ORCID 0000-0001-8876-5099
Yi Zhang *Department of General Surgery, Cancer Center, Peking University Third Hospital, Beijing, 100191, China.
Jie CaiLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Bipin RimalCenter for Molecular Toxicology and Carcinogenesis, Department of Veterinary & Biomedical Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
Edson R RochaDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC, 27834, USA.
James P ColemanDepartment of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, NC, 27834, USA.
Chenran ZhangLaboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Robert G NicholsCenter for Molecular Toxicology and Carcinogenesis, Department of Veterinary & Biomedical Sciences, Pennsylvania State University, University Park, PA, 16802, USA.
Yuhong LuoLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.ORCID 0000-0001-8273-8380
Bora KimLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Yaozong ChenLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.ORCID 0000-0001-5380-2339
Kristopher W KrauszLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.
Curtis C HarrisLaboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA.ORCID 0000-0001-5268-0181
Andrew D PattersonCenter for Molecular Toxicology and Carcinogenesis, Department of Veterinary & Biomedical Sciences, Pennsylvania State University, University Park, PA, 16802, USA. adp117@psu.edu.ORCID 0000-0003-2073-0070
Zhipeng ZhangDepartment of General Surgery, Cancer Center, Peking University Third Hospital, Beijing, 100191, China. zhangzhipeng06@126.com.
Shogo TakahashiLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA. shogo.takahashi@nih.gov.ORCID 0000-0002-3831-5353
Frank J GonzalezLaboratory of Metabolism, Center for Cancer Research, National Cancer Institute, Bethesda, MD, 20892, USA. gonzalef@mail.nih.gov.ORCID 0000-0002-7990-2140
National Cancer Institute · USPennsylvania State University · USEast Carolina University · USPeking University · CN

Funding

Xenobiotic receptorsZIABC005562 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GONZALEZ, FRANK J · 2009 to 2025
$26.9M
Precision Medicine of CancerZIABC011492 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HARRIS, CURTIS · 2013 to 2025
$23.2M
Xenobiotic ReceptorsZIABC005708 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GONZALEZ, FRANK J · 2009 to 2025
$16.4M
R01: FXR and the Gut Microbiome as Modulators of Non-Alcoholic Fatty Liver DiseaseU01DK119702 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI PATTERSON, ANDREW · 2019 to 2023
$1.5M
Intramural NIH HHS ZIA BC005562NIDDK NIH HHS U01 DK119702
6 · The paper itself

Abstract

Bile salt hydrolase (BSH) in Bacteroides is considered a potential drug target for obesity-related metabolic diseases, but its involvement in colon tumorigenesis has not been explored. BSH-expressing Bacteroides is found at high abundance in the stools of colorectal cancer (CRC) patients  with overweight and in the feces of a high-fat diet (HFD)-induced CRC mouse model. Colonization of B. fragilis 638R, a strain with low BSH activity, overexpressing a recombinant bsh gene from B. fragilis NCTC9343 strain, results in increased unconjugated bile acids in the colon and accelerated progression of CRC under HFD treatment. In the presence of high BSH activity, the resultant elevation of unconjugated deoxycholic acid and lithocholic acid activates the G-protein-coupled bile acid receptor, resulting in increased β-catenin-regulated chemokine (C-C motif) ligand 28 (CCL28) expression in colon tumors. Activation of the β-catenin/CCL28 axis leads to elevated intra-tumoral immunosuppressive CD25

Indexed as

Colonic NeoplasmsColorectal NeoplasmsAmidohydrolasesAnimalsBacteroidesbeta CateninBile Acids and SaltsCarcinogenesisMiceObesityAmidohydrolasesbeta CateninBile Acids and Saltscholoylglycine hydrolase

Identifiers

PMID36765047
PMCPMC9918522
OpenAlexW4319959122

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.