Evidence map›Paper›PMID 28460056›Full record

ArticleHuman molecular genetics2017

Dimethyl fumarate mediates Nrf2-dependent mitochondrial biogenesis in mice and humans.

Genki Hayashi, Mittal Jasoliya, Sunil Sahdeo, Francesco Saccà, Chiara Pane, Alessandro Filla, Angela Marsili, Giorgia Puorro, Roberta Lanzillo, Vincenzo Brescia Morra and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Human molecular genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

90 citing papers in PubMed, 129 citations in OpenAlex.

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30 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

11 authors at 3 institutions in 2 countries.

Genki HayashiDepartment of Molecular Biosciences, University of California, Davis, 95616 CA, USA.
Mittal JasoliyaDepartment of Molecular Biosciences, University of California, Davis, 95616 CA, USA.
Sunil SahdeoJanssen Pharmaceuticals, 3210 Merryfield Row, San Diego, 92121 CA, USA.
Francesco SaccàDepartment of Neurosciences, Odontostomatological and Reproductive Sciences, University Federico II, Naples 80131, Italy.
Chiara PaneDepartment of Neurosciences, Odontostomatological and Reproductive Sciences, University Federico II, Naples 80131, Italy.
Alessandro FillaDepartment of Neurosciences, Odontostomatological and Reproductive Sciences, University Federico II, Naples 80131, Italy.
Angela MarsiliDepartment of Neurosciences, Odontostomatological and Reproductive Sciences, University Federico II, Naples 80131, Italy.
Giorgia PuorroDepartment of Neurosciences, Odontostomatological and Reproductive Sciences, University Federico II, Naples 80131, Italy.
Roberta LanzilloDepartment of Neurosciences, Odontostomatological and Reproductive Sciences, University Federico II, Naples 80131, Italy.
Vincenzo Brescia MorraDepartment of Neurosciences, Odontostomatological and Reproductive Sciences, University Federico II, Naples 80131, Italy.
Gino CortopassiDepartment of Molecular Biosciences, University of California, Davis, 95616 CA, USA.
Federico II University Hospital · ITUniversity of California, Davis · USJanssen (United States) · US

Funding

TRANSLOCATION OF p66Shc: KINETICS, FUNCTION, APOPTOSISP01AG025532 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KIM, KYOUNGMI · 2007 to 2017
$12.1M
MITOCHONDRIAL MECHANISMS IN OPTIC NEUROPATHYR01EY012245 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI CORTOPASSI, GINO A · 2000 to 2016
$5.1M
Predoctoral Training in Pharmacological SciencesT32GM099608 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2021
$2.2M
Mitochondrial Iron-Sulfur cluster mechanisms and therapy in Friedreich's ataxiaR01NS077777 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI CORTOPASSI, GINO A · 2011 to 2015
$1.8M
NEI NIH HHS R01 EY012245NIA NIH HHS P01 AG025532NIGMS NIH HHS T32 GM099608NINDS NIH HHS R01 NS077777
6 · The paper itself

Abstract

The induction of mitochondrial biogenesis could potentially alleviate mitochondrial and muscle disease. We show here that dimethyl fumarate (DMF) dose-dependently induces mitochondrial biogenesis and function dosed to cells in vitro, and also dosed in vivo to mice and humans. The induction of mitochondrial gene expression is more dependent on DMF's target Nrf2 than hydroxycarboxylic acid receptor 2 (HCAR2). Thus, DMF induces mitochondrial biogenesis primarily through its action on Nrf2, and is the first drug demonstrated to increase mitochondrial biogenesis with in vivo human dosing. This is the first demonstration that mitochondrial biogenesis is deficient in Multiple Sclerosis patients, which could have implications for MS pathophysiology and therapy. The observation that DMF stimulates mitochondrial biogenesis, gene expression and function suggests that it could be considered for mitochondrial disease therapy and/or therapy in muscle disease in which mitochondrial function is important.

Indexed as

Dimethyl FumarateNF-E2-Related Factor 2AnimalsCell Culture TechniquesFibroblastsHumansMiceMitochondriaMultiple SclerosisNeuroprotective AgentsOrganelle BiogenesisDimethyl FumarateNeuroprotective AgentsNFE2L2 protein, humanNfe2l2 protein, mouseNF-E2-Related Factor 2

Identifiers

PMID28460056
PMCPMC6251607
OpenAlexW2607554518

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.