Evidence map›Paper›PMID 29073080›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Maladaptive DNA repair is the ultimate contributor to the death of trimethoprim-treated cells under aerobic and anaerobic conditions.

Xavier Giroux, Wei-Lin Su, Marie-Florence Bredeche, Ivan Matic

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

43 citing papers in PubMed, 72 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Xavier GirouxFaculté de Médecine Paris Descartes, INSERM U1001, Sorbonne Paris Cité, Université Paris Descartes, 75014 Paris, France.
Wei-Lin SuFaculté de Médecine Paris Descartes, INSERM U1001, Sorbonne Paris Cité, Université Paris Descartes, 75014 Paris, France.
Marie-Florence BredecheFaculté de Médecine Paris Descartes, INSERM U1001, Sorbonne Paris Cité, Université Paris Descartes, 75014 Paris, France.
Ivan MaticFaculté de Médecine Paris Descartes, INSERM U1001, Sorbonne Paris Cité, Université Paris Descartes, 75014 Paris, France; ivan.matic@inserm.fr.
Inserm · FRDélégation Paris 5 · FRSorbonne Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bactericidal effects of antibiotics are undoubtedly triggered by target-specific interactions, but there is growing evidence that an important aspect of cytotoxicity results from treatment-induced metabolic perturbations. In this study, we characterized molecular mechanisms whereby trimethoprim treatment results in cell death, using

Indexed as

AerobiosisAnaerobiosisAnti-Infective Agents, UrinaryDeoxyguanosineDNA, BacterialDNA DamageDNA MethylationDNA RepairDNA ReplicationEscherichia coliGene Expression Regulation, BacterialReactive Oxygen SpeciesSOS Response, GeneticsThymidineTrimethoprimAnti-Infective Agents, UrinaryDeoxyguanosineDNA, BacterialReactive Oxygen SpeciesThymidineTrimethoprimantibioticDNA repairnitrate respirationoxidative stresstrimethoprim

Identifiers

PMID29073080
PMCPMC5664507
OpenAlexW2763080719

What OpenQuestion holds

Textmetadata
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.