Evidence map›Paper›PMID 32404351›Full record

ArticleDiabetes2020

Endothelial Overexpression of Metallothionein Prevents Diabetes-Induced Impairment in Ischemia Angiogenesis Through Preservation of HIF-1α/SDF-1/VEGF Signaling in Endothelial Progenitor Cells.

Kai Wang, Xiaozhen Dai, Junhong He, Xiaoqing Yan, Chengkui Yang, Xia Fan, Shiyue Sun, Jing Chen, Jianxiang Xu, Zhongbin Deng and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 59 citations in OpenAlex.

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  17. Endothelial progenitor cells in pregnancy-related diseases.Clinical science (London, England : 1979) · 2023
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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

20 authors at 5 institutions in 2 countries.

Kai WangDepartment of Pediatrics, Endocrinology and Metabolism, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xiaozhen DaiSchool of Bioscience and Technology, Chengdu Medical College, Chengdu, China.
Junhong HePediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY.
Xiaoqing YanChinese-American Research Institute for Diabetic Complications, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Chengkui YangPediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY.
Xia FanChinese-American Research Institute for Diabetic Complications, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Shiyue SunChinese-American Research Institute for Diabetic Complications, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, China.
Jing ChenPediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY.
Jianxiang XuPediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY.
Zhongbin DengDepartment of Medicine, School of Medicine, University of Louisville, Louisville, KY.
Jiawei FanSchool of Bioscience and Technology, Chengdu Medical College, Chengdu, China.
Xiaohuan YuanPediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY.
Hairong LiuExperimental Research Center, the First Affiliated Hospital, Chengdu Medical College, Chengdu, Sichuan, China.
Edward C CarlsonDepartment of Biomedical Sciences, University of North Dakota, Grand Forks, ND.
Feixia ShenDepartment of Pediatrics, Endocrinology and Metabolism, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Kupper A WintergerstPediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY.
Daniel J ConklinDepartment of Medicine, School of Medicine, University of Louisville, Louisville, KY.
Paul N EpsteinPediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY.ORCID 0000-0002-8385-9982
Chaosheng LuDepartment of Pediatrics, Endocrinology and Metabolism, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Yi TanPediatric Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY y0tan002@louisville.edu.ORCID 0000-0002-9798-6237
University of Louisville · USWenzhou Medical University · CNChengdu Medical College · CNFirst Affiliated Hospital of Chengdu Medical College · CNUniversity of North Dakota · US

Funding

Project 5 - Metabolomic Analysis of AtherothrombosisP20GM103492 · NIGMS · UNIVERSITY OF LOUISVILLE · PI DEFILIPPIS, ANDREW · 2012 to 2017
$13.8M
TBDP30GM127607 · NIGMS · UNIVERSITY OF LOUISVILLE · PI HILL, BRADFORD GUY · 2018 to 2022
$6.3M
CSN8 regulation of S1P-enriched extracellular vesicles to modulate NAFLD by gut-liver axisR01DK115406 · NIDDK · UNIVERSITY OF LOUISVILLE · PI DENG, ZHONG-BIN · 2018 to 2022
$2.0M
Gut extracellular vesicles promote alcohol-induced liver injury via TLR4-regulated miRNAsR21AA025724 · NIAAA · UNIVERSITY OF LOUISVILLE · PI DENG, ZHONG-BIN · 2018 to 2019
$558k
Intestinal epithelial cells-derived exosomal miRNAs regulate liver inflammation in obesityR21AI128206 · NIAID · UNIVERSITY OF LOUISVILLE · PI DENG, ZHONG-BIN · 2017 to 2018
$424k
NIAAA NIH HHS R21 AA025724NIAID NIH HHS R21 AI128206NIDDK NIH HHS R01 DK115406NIGMS NIH HHS P20 GM103492NIGMS NIH HHS P30 GM127607
6 · The paper itself

Abstract

Diabetes-induced oxidative stress is one of the major contributors to dysfunction of endothelial progenitor cells (EPCs) and impaired endothelial regeneration. Thus, we tested whether increasing antioxidant protein metallothionein (MT) in EPCs promotes angiogenesis in a hind limb ischemia (HLI) model in endothelial MT transgenic (JTMT) mice with high-fat diet- and streptozocin-induced diabetes. Compared with littermate wild-type (WT) diabetic mice, JTMT diabetic mice had improved blood flow recovery and angiogenesis after HLI. Similarly, transplantation of JTMT bone marrow-derived mononuclear cells (BM-MNCs) stimulated greater blood flow recovery in

Indexed as

AnimalsBlotting, WesternCell SurvivalChemokine CXCL12Diabetes Mellitus, ExperimentalEndothelial Progenitor CellsEnzyme-Linked Immunosorbent AssayFemaleHindlimbHypoxia-Inducible Factor 1, alpha SubunitIschemiaLeukocytes, MononuclearMaleMetallothioneinMiceNeovascularization, PathologicChemokine CXCL12Hypoxia-Inducible Factor 1, alpha SubunitMetallothioneinRNA, Small InterferingVascular Endothelial Growth Factor A

Identifiers

PMID32404351
PMCPMC7519474
OpenAlexW3024667974

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.