Evidence map›Paper›PMID 29149759›Full record

ArticleRedox biology2018

DUSP1 alleviates cardiac ischemia/reperfusion injury by suppressing the Mff-required mitochondrial fission and Bnip3-related mitophagy via the JNK pathways.

Qinhua Jin, Ruibing Li, Nan Hu, Ting Xin, Pingjun Zhu, Shunying Hu, Sai Ma, Hong Zhu, Jun Ren, Hao Zhou

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 258 papers.

0numbers the graph read from it
0cells of the map it votes in
258citing papers in PubMed
21.3field-weighted citation impact, top 1% 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

258 citing papers in PubMed, 455 citations in OpenAlex.

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  17. Mitochondrial Quality Control and Cell Death.International journal of molecular sciences · 2025
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198 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

10 authors at 2 institutions in 2 countries.

Qinhua JinChinese PLA General Hospital, Medical School of Chinese PLA, Beijing 100853, China.
Ruibing LiChinese PLA General Hospital, Medical School of Chinese PLA, Beijing 100853, China; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.
Nan HuCenter for Cardiovascular Research and Alternative Medicine, Wyoming University, Laramie, WY 82071, USA.
Ting XinChinese PLA General Hospital, Medical School of Chinese PLA, Beijing 100853, China; Department of Cardiology, Tianjin First Central Hospital, Tianjin 300192, China.
Pingjun ZhuChinese PLA General Hospital, Medical School of Chinese PLA, Beijing 100853, China.
Shunying HuChinese PLA General Hospital, Medical School of Chinese PLA, Beijing 100853, China.
Sai MaCenter for Cardiovascular Research and Alternative Medicine, Wyoming University, Laramie, WY 82071, USA.
Hong ZhuCenter for Cardiovascular Research and Alternative Medicine, Wyoming University, Laramie, WY 82071, USA.
Jun RenCenter for Cardiovascular Research and Alternative Medicine, Wyoming University, Laramie, WY 82071, USA.
Hao ZhouChinese PLA General Hospital, Medical School of Chinese PLA, Beijing 100853, China; Center for Cardiovascular Research and Alternative Medicine, Wyoming University, Laramie, WY 82071, USA. Electronic address: zhouhao301@outlook.com.
Chinese PLA General Hospital · CNUniversity of Wyoming · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial fission and selective mitochondrial autophagy (mitophagy) form an essential axis of mitochondrial quality control that plays a critical role in the development of cardiac ischemia-reperfusion (IR) injury. However, the precise upstream molecular mechanism of fission/mitophagy remains unclear. Dual-specificity protein phosphatase1 (DUSP1) regulates cardiac metabolism, but its physiological contribution in the reperfused heart, particularly its influence on mitochondrial homeostasis, is unknown. Here, we demonstrated that cardiac DUSP1 was downregulated following acute cardiac IR injury. In vivo, compared to wild-type mice, DUSP1 transgenic mice (DUSP1

Indexed as

MAP Kinase Signaling SystemMitochondrial DynamicsMitophagyAnimalsDual Specificity Phosphatase 1Membrane ProteinsMice, TransgenicMitochondria, HeartMitochondrial ProteinsMyocardial Reperfusion InjuryMyocardiumBNip3 protein, mouseDual Specificity Phosphatase 1Dusp1 protein, mouseMembrane Proteinsmitochondrial fission factor, mouseMitochondrial ProteinsBnip3Cardiac IR injuryDUSP1JNKMffMitochondrial fissionMitophagy

Identifiers

PMID29149759
PMCPMC5691221
OpenAlexW2768024671

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.