Evidence map›Paper›PMID 42446156›Full record

ArticleJournal of cellular and molecular medicine2026

Myeloid-Derived Growth Factor Improves Endothelial Progenitor Cell Function and Angiogenesis in Mice With Diabetic Hindlimb Ischemia by Activating Akt/HIF-1α Signalling Pathway.

Wen Mei, Biying Meng, Bilin Zhang, Yi Shu, Haizhao Luo, Jingwen Ye, Yijiang Hou, Biao Zhu, Jiajia Zhang

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Wen MeiDepartment of Endocrinology, School of Medicine, the Sixth Affiliated Hospital of South China University of Technology (Nanhai District People's Hospital of Foshan), Foshan, China.
Biying MengDepartment of Endocrinology, General Hospital of Central Theater Command, Wuhan, China.
Bilin ZhangDepartment of Endocrinology, General Hospital of Central Theater Command, Wuhan, China.
Yi ShuDepartment of Endocrinology, School of Medicine, the Sixth Affiliated Hospital of South China University of Technology (Nanhai District People's Hospital of Foshan), Foshan, China.ORCID 0000-0002-5047-0276
Haizhao LuoDepartment of Endocrinology, School of Medicine, the Sixth Affiliated Hospital of South China University of Technology (Nanhai District People's Hospital of Foshan), Foshan, China.ORCID 0009-0003-2984-8398
Jingwen YeDepartment of Endocrinology, School of Medicine, the Sixth Affiliated Hospital of South China University of Technology (Nanhai District People's Hospital of Foshan), Foshan, China.ORCID 0000-0002-8744-0687
Yijiang HouDepartment of Endocrinology, General Hospital of Central Theater Command, Wuhan, China.
Biao ZhuDepartment of Stomatology, Fuxing Hospital, Capital Medical University, Beijing, China.ORCID 0000-0003-3794-1499
Jiajia ZhangDepartment of Endocrinology, General Hospital of Central Theater Command, Wuhan, China.ORCID 0009-0008-9665-7432

Funding

National Natural Science Foundation of China NSFC 82300931Natural Science Foundation of Hubei Province of China 2024AFB1072the Medical Science and Technology Research Foundation of Guangdong Province A2023325
6 · The paper itself

Abstract

Myeloid-derived growth factor (MYDGF) offers new insights into inflammation and endothelial function, yet its role in endothelial progenitor cells (EPCs) and diabetes-related hindlimb ischemia (DLI) remains unclear. In this study, we found that MYDGF depletion impaired the angiogenic function of EPCs, leading to reduced vascularisation and decreased blood flow in diabetic mice with hindlimb ischemia. Conversely, treatment with adeno-associated virus-mediated MYDGF restored vascularisation and improved blood perfusion. In vitro, treatment with recombinant MYDGF attenuated EPC dysfunction, apoptosis and inflammatory responses. Mechanistic studies revealed that these protective effects were mediated via the AKT/HIF-1α pathway, and silencing HIF-1α abrogated the benefits of MYDGF both in vivo and in vitro. Together, these findings identified MYDGF as a potential therapeutic target for DLI.

Indexed as

AngiogenesisDiabetes Mellitus, ExperimentalEndothelial Progenitor CellsHindlimbHypoxia-Inducible Factor 1, alpha SubunitIschemiaNeovascularization, PhysiologicProto-Oncogene Proteins c-aktSignal TransductionAnimalsApoptosisMaleMiceMice, Inbred C57BLHypoxia-Inducible Factor 1, alpha SubunitProto-Oncogene Proteins c-aktangiogenesisdiabetic limb ischemiaendothelial progenitor cellsmyeloid‐derived growth factor

Identifiers

PMID42446156
PMCPMC13367132

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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.