Evidence map›Paper›PMID 28348719›Full record

ArticleOxidative medicine and cellular longevity2017

BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage.

Li-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, Kousar Rizwana, Jia-Hong Lu, Jian-Guang Tang, Bo Jiang, Xiang-Min Shen, Ji-Feng Guo, Bei-Sha Tang and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  8. PARK7/DJ-1 as a Therapeutic Target in Gut-Brain Axis Diseases.International journal of molecular sciences · 2022
    Review
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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

12 authors at 3 institutions in 5 countries.

Li-Xia QinDepartment of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0002-3050-3181
Jie-Qiong TanThe State Key Laboratory of Medical Genetics and School of Life Science, Central South University, Changsha, Hunan, China.
Hai-Nan ZhangDepartment of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China.
Kousar RizwanaDepartment of Biology, Allama Iqbal Open University, Islamabad, Pakistan.
Jia-Hong LuState Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao, China.
Jian-Guang TangDepartment of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China.
Bo JiangDepartment of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China.
Xiang-Min ShenDepartment of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China.
Ji-Feng GuoThe State Key Laboratory of Medical Genetics and School of Life Science, Central South University, Changsha, Hunan, China; Department of Neurology, Xiangya Hospital, Central South University, Changsha, China; Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, China; Neurodegenerative Disorders Research Center, Central South University, Changsha, China.
Bei-Sha TangThe State Key Laboratory of Medical Genetics and School of Life Science, Central South University, Changsha, Hunan, China; Department of Neurology, Xiangya Hospital, Central South University, Changsha, China; Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, China; Neurodegenerative Disorders Research Center, Central South University, Changsha, China.
Li-Ming TanDepartment of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China.
Chun-Yu WangDepartment of Neurology, The Second Xiangya Hospital, Central South University, Changsha, China.ORCID 0000-0003-1629-0885
Central South University · CNAllama Iqbal Open University · PKUniversity of Macau · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Loss-of-function mutations in gene encoding DJ-1 contribute to the pathogenesis of autosomal recessive early-onset familial forms of Parkinson's disease (PD). DJ-1 is a multifunctional protein and plays a protective role against oxidative stress-induced mitochondrial damage and cell death, but the exact mechanism underlying this is not yet clearly understood. Here, using coimmunoprecipitation (Co-IP) and immunofluorescence methods, we prove that Bcl-2-associated athanogene 5 (BAG5), a BAG family member, interacts with DJ-1 in mammalian cells. Moreover, we show that BAG5 could decrease stability of DJ-1 and weaken its role in mitochondrial protection probably by influencing dimerization in stress condition. Our study reveals the relationship of BAG5 and DJ-1 suggesting a potential role for BAG5 in the pathogenesis of PD through its functional interactions with DJ-1.

Indexed as

Oxidative StressAdaptor Proteins, Signal TransducingApoptosisHEK293 CellsHSP70 Heat-Shock ProteinsHumansImmunoprecipitationMembrane Potential, MitochondrialMicroscopy, FluorescenceMitochondriaNeuroprotective AgentsProtein Deglycase DJ-1Reactive Oxygen SpeciesRNA InterferenceRNA, Small InterferingRotenoneAdaptor Proteins, Signal TransducingBAG5 protein, humanHSP70 Heat-Shock ProteinsNeuroprotective AgentsProtein Deglycase DJ-1Reactive Oxygen SpeciesRNA, Small InterferingRotenone

Identifiers

PMID28348719
PMCPMC5352890
OpenAlexW2594512546

What OpenQuestion holds

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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.