Evidence map›Paper›PMID 33553168›Full record

ArticleFrontiers in cell and developmental biology2020

Mst1 Knockout Alleviates Mitochondrial Fission and Mitigates Left Ventricular Remodeling in the Development of Diabetic Cardiomyopathy.

Xinyu Feng, Shanjie Wang, Xingjun Yang, Jie Lin, Wanrong Man, Yuan Dong, Yan Zhang, Zhijing Zhao, Haichang Wang, Dongdong Sun

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Review
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  9. Mitochondrial Dysfunction in HFpEF: Potential Interventions Through Exercise.Journal of cardiovascular translational research · 2025
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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

10 authors.

Xinyu FengHeart Hospital, Xi'an International Medical Center, Xi'an, China.
Shanjie WangDepartment of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xingjun YangDepartment of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Jie LinDepartment of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Wanrong ManDepartment of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yuan DongDepartment of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yan ZhangDepartment of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Zhijing ZhaoDepartment of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Haichang WangHeart Hospital, Xi'an International Medical Center, Xi'an, China.
Dongdong SunHeart Hospital, Xi'an International Medical Center, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The disruption of mitochondrial dynamics is responsible for the development of diabetic cardiomyopathy (DCM). However, the mechanisms that regulate the balance of mitochondrial fission and fusion are not well-understood. Wild-type, Mst1 transgenic and Mst1 knockout mice were induced with experimental diabetes by streptozotocin injection. In addition, primary neonatal cardiomyocytes were isolated and cultured to simulate diabetes to explore the mechanisms. Echocardiograms and hemodynamic measurements revealed that Mst1 knockout alleviated left ventricular remodeling and cardiac dysfunction in diabetic mice. Mst1 knockdown significantly decreased the number of TUNEL-positive cardiomyocytes subjected to high-glucose (HG) medium culture. Immunofluorescence study indicated that Mst1 overexpression enhanced, while Mst1 knockdown mitigated mitochondrial fission in DCM. Mst1 participated in the regulation of mitochondrial fission by upregulating the expression of Drp1, activating Drp1

Indexed as

DCMDiabetic CardiomyopathyMammalian Sterile 20-like Kinase 1Mitochondrial DysfunctionMitochondrial FissionMitochondrial FusionMst1

Identifiers

PMID33553168
PMCPMC7859113

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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.