Evidence map›Paper›PMID 33664385›Full record

ArticleCommunications biology2021

Entropy-driven binding of gut bacterial β-glucuronidase inhibitors ameliorates irinotecan-induced toxicity.

Hsien-Ya Lin, Chia-Yu Chen, Ting-Chien Lin, Lun-Fu Yeh, Wei-Che Hsieh, Shijay Gao, Pierre-Alain Burnouf, Bing-Mae Chen, Tung-Ju Hsieh, Punsaldulam Dashnyam and 4 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 34 citations in OpenAlex.

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  12. Targeted inhibition of Gus-expressingActa pharmaceutica Sinica. B · 2024
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  17. A Review of Gut Microbiota-Derived Metabolites in Tumor Progression and Cancer Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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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

14 authors at 4 institutions in 1 country.

Hsien-Ya Lin *Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-3922-1797
Chia-Yu Chen *Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-1324-1394
Ting-Chien Lin *Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Lun-Fu YehInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Wei-Che HsiehInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Shijay GaoInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Pierre-Alain BurnoufInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Bing-Mae ChenInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Tung-Ju HsiehInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Punsaldulam DashnyamInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Yen-Hsi KuoInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Zhijay TuInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-3531-9439
Steve R RofflerInstitute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan. sroff@ibms.sinica.edu.tw.ORCID 0000-0003-2543-7295
Chun-Hung LinInstitute of Biological Chemistry, Academia Sinica, Taipei, Taiwan. chunhung@gate.sinica.edu.tw.ORCID 0000-0002-6795-8825
Institute of Biological Chemistry, Academia Sinica · TWNational Taiwan University · TWInstitute of Biomedical Sciences, Academia Sinica · TWKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Irinotecan inhibits cell proliferation and thus is used for the primary treatment of colorectal cancer. Metabolism of irinotecan involves incorporation of β-glucuronic acid to facilitate excretion. During transit of the glucuronidated product through the gastrointestinal tract, an induced upregulation of gut microbial β-glucuronidase (GUS) activity may cause severe diarrhea and thus force many patients to stop treatment. We herein report the development of uronic isofagomine (UIFG) derivatives that act as general, potent inhibitors of bacterial GUSs, especially those of Escherichia coli and Clostridium perfringens. The best inhibitor, C6-nonyl UIFG, is 23,300-fold more selective for E. coli GUS than for human GUS (K

Indexed as

IrinotecanAnimalsBacteriaCell LineColonDiarrheaDisease Models, AnimalEnzyme InhibitorsFemaleGastrointestinal MicrobiomeGlucuronidaseHumansImino PyranosesMiceMice, Inbred BALB CUronic AcidsEnzyme InhibitorsGlucuronidaseImino PyranosesIrinotecanisofagomineUronic Acids

Identifiers

PMID33664385
PMCPMC7933434
OpenAlexW3135748610

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.