Evidence map›Paper›PMID 25164363›Full record

ArticleScientific reports2014

A novel molecule Me6TREN promotes angiogenesis via enhancing endothelial progenitor cell mobilization and recruitment.

Haixu Chen, Sihan Wang, Jing Zhang, Xiangliang Ren, Rui Zhang, Wei Shi, Yang Lv, Yong Zhou, Xinlong Yan, Lin Chen and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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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

16 authors at 2 institutions in 1 country.

Haixu Chen1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Sihan Wang1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Jing Zhang1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Xiangliang Ren1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Rui Zhang1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Wei Shi1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Yang Lv1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Yong ZhouLaboratory of Blood-borne Virus, Beijing Institute of Transfusion Medicine, Beijing 100850, China.
Xinlong Yan1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Lin Chen1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Lijuan He1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Bowen Zhang1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Xue Nan1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Wen Yue1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Yanhua Li1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Xuetao Pei1] Stem Cell and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing 100850, China [2] South China Research Center for Stem Cell &Regenerative Medicine, AMMS, Guangzhou 510005, China.
Center for High Pressure Science & Technology Advanced Research · CNGuangzhou Blood Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Critical limb ischaemia is the most severe clinical manifestation of peripheral arterial disease. The circulating endothelial progenitor cells (EPCs) play important roles in angiogenesis and ischemic tissue repair. The increase of circulating EPC numbers by using mobilization agents is critical for obtaining a better therapeutic outcome in patients with ischemic disease. Here, we firstly report a novel small molecule, Me6TREN (Me6), can efficiently mobilize EPCs into the blood circulation. Single injection of Me6 induced a long-lasting increase in circulating Flk-1(+) Sca-1(+) EPC numbers. In a mouse hind limb ischemia (HLI) model, local intramuscular transplantation of these Me6-mobilized cells accelerated the blood flow restoration in the ischemic muscles. More importantly, systemic administration of Me6 notably increased the capillary density, arteriole density and regenerative muscle weight in the ischemic tissue of HLI. Mechanistically, we found Me6 reduced stromal cell-derived factor-1α level in bone marrow by up-regulation of matrix metallopeptidase-9 expression, which allowed the dissemination of EPCs into peripheral blood. These data indicate that Me6 may represent a potentially useful therapy for ischemic disease via enhancing autologous EPC recruitment and promote angiogenesis.

Indexed as

Angiogenesis Inducing AgentsAnimalsApoptosisCell MovementCell ProliferationCells, CulturedChemokine CXCL12Endothelial Progenitor CellsEnzyme InductionEthylaminesHindlimbHuman Umbilical Vein Endothelial CellsIschemiaMaleMatrix Metalloproteinase 9Mice, Inbred C57BLAngiogenesis Inducing AgentsChemokine CXCL12EthylaminesMatrix Metalloproteinase 9Mmp9 protein, mousetris(2-(dimethylamino)ethyl)amine

Identifiers

PMID25164363
PMCPMC5385830
OpenAlexW2056153152

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.