Evidence map›Paper›PMID 34830106›Full record

ArticleInternational journal of molecular sciences2021

A Yeast-Based Repurposing Approach for the Treatment of Mitochondrial DNA Depletion Syndromes Led to the Identification of Molecules Able to Modulate the dNTP Pool.

Giulia di Punzio, Micol Gilberti, Enrico Baruffini, Tiziana Lodi, Claudia Donnini, Cristina Dallabona

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  4. Genes · 2021
    Review
  5. 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

6 authors at 1 institution in 1 country.

Giulia di PunzioDepartment of Chemistry Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.ORCID 0000-0002-7705-2971
Micol GilbertiDepartment of Chemistry Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.
Enrico BaruffiniDepartment of Chemistry Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.ORCID 0000-0002-8280-7849
Tiziana LodiDepartment of Chemistry Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.
Claudia DonniniDepartment of Chemistry Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.ORCID 0000-0002-4901-2358
Cristina DallabonaDepartment of Chemistry Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.ORCID 0000-0003-4397-9143
University of Parma · IT

Funding

'Departments of Excellence' program COMP-HUB InitiativeItalian Ministry of Health GR-2016-02361449Telethon Foundation GGP15041Telethon Foundation GGP19287AUniversity of Parma BARUFFINI_2019_FIL_PROGETTI_B_CARIPR_COFIN
6 · The paper itself

Abstract

Mitochondrial DNA depletion syndromes (MDS) are clinically heterogenous and often severe diseases, characterized by a reduction of the number of copies of mitochondrial DNA (mtDNA) in affected tissues. In the context of MDS, yeast has proved to be both an excellent model for the study of the mechanisms underlying mitochondrial pathologies and for the discovery of new therapies via high-throughput assays. Among the several genes involved in MDS, it has been shown that recessive mutations in MPV17 cause a hepatocerebral form of MDS and Navajo neurohepatopathy. MPV17 encodes a non selective channel in the inner mitochondrial membrane, but its physiological role and the nature of its cargo remains elusive. In this study we identify ten drugs active against MPV17 disorder, modelled in yeast using the homologous gene

Indexed as

DNA, FungalDNA, MitochondrialHeredodegenerative Disorders, Nervous SystemLiver DiseasesMembrane ProteinsMitochondriaMitochondrial DiseasesMitochondrial ProteinsPeripheral Nervous System DiseasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsHumansNucleotidesSyndromeDNA, FungalDNA, MitochondrialMembrane ProteinsMitochondrial ProteinsMPV17 protein, humanNucleotidesSaccharomyces cerevisiae ProteinsSYM1 protein, S cerevisiaedrug repurposingMIP1mitochondrial DNA depletion syndromes (MDS)mitochondrial dNTP poolMPV17POLGRNR2RRM2BSYM1yeast

Identifiers

PMID34830106
PMCPMC8621932
OpenAlexW3211344624

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.