Evidence map›Paper›PMID 28317877›Full record

ArticleScientific reports2017

Transcription factor NF-kappa B represses ANT1 transcription and leads to mitochondrial dysfunctions.

Chen Zhang, Hui Jiang, Pin Wang, Heng Liu, Xiulian Sun

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

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  5. Novel gene signatures predicting and immune infiltration analysis in Parkinson's disease: based on combining random forest with artificial neural network.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
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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

5 authors at 2 institutions in 1 country.

Chen ZhangDepartment of Neurology, Qilu Hospital of Shandong University, No. 107 West Wenhua Road, Jinan, 250012, Shandong Province, China.
Hui JiangDepartment of Pediatrics, 2nd Hospital of Shandong University, No. 44 West Wenhua Road, Jinan, 250011, Shandong Province, China.
Pin WangOtolaryngology Key, Lab of Ministry of Health, No. 44 West Wenhua Road, Jinan, China.
Heng LiuOtolaryngology Key, Lab of Ministry of Health, No. 44 West Wenhua Road, Jinan, China.
Xiulian SunBrain Research Institute, Qilu Hospital of Shandong University, No.107 West Wenhua Road, Jinan, 250012, Shandong Province, China.
Qilu Hospital of Shandong University · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondria are intracellular organelles involved in cell survival and death, and dysfunctions of mitochondria are related to neurodegenerative diseases. As the most abundant protein in the mitochondrial inner membrane, adenine nucleotide translocator 1 (ANT1) plays a critical role in mitochondrial function, including the exchange of adenosine triphosphate/adenosine diphosphate (ATP/ADP) in mitochondria, basal proton leak and mitochondrial permeability transition pore (mPTP). Here, we show that ANT1 transcription is regulated by transcription factor NF-kappa B (NF-κB). NF-κB is bound to two NF-κB responsive elements (NREs) located at +1 to +20 bp and +41 to +61 bp in the ANT1 promoter. An NF-κB signalling stimulator, tumour necrosis factor alpha (TNFα), suppresses ANT1 mRNA and protein expression. Activation of NF-κB by TNFα impairs ATP/ADP exchange and decreases ATP production in mitochondria. Activation of NF-κB by TNFα decreases calcium induced mPTP opening, elevates mitochondrial potential and increases reactive oxygen species (ROS) production in both T98G human glioblastoma cells and rat cortical neurons. These results demonstrate that NF-κB signalling may repress ANT1 gene transcription and impair mitochondrial functions.

Indexed as

Transcription, GeneticAdenine Nucleotide Translocator 1Adenosine DiphosphateAdenosine TriphosphateBase SequenceCalciumHEK293 CellsHumansMembrane Potential, MitochondrialMitochondriaMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreNF-kappa BPromoter Regions, GeneticReactive Oxygen SpeciesResponse ElementsAdenine Nucleotide Translocator 1Adenosine DiphosphateAdenosine TriphosphateCalciumMitochondrial Membrane Transport ProteinsMitochondrial Permeability Transition PoreNF-kappa BReactive Oxygen SpeciesSLC25A4 protein, human

Identifiers

PMID28317877
PMCPMC5357787
OpenAlexW2602809814

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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.