Evidence map›Paper›PMID 24663037›Full record

ArticlePloS one2014

Human urine-derived stem cells alone or genetically-modified with FGF2 Improve type 2 diabetic erectile dysfunction in a rat model.

Bin Ouyang, Xiangzhou Sun, Dayu Han, Shenfu Chen, Bing Yao, Yong Gao, Jun Bian, Yanping Huang, Yadong Zhang, Zi Wan and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 3 pooled it
7.6field-weighted citation impact, top 2% 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

66 citing papers in PubMed, 3 syntheses or guidelines pooled it, 120 citations in OpenAlex.

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6 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

16 authors at 5 institutions in 2 countries.

Bin OuyangDepartment of Urology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Xiangzhou SunDepartment of Urology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Dayu HanDepartment of Urology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Shenfu ChenDepartment of Urology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Bing YaoDepartment of Urology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Yong GaoReproductive Medicine Center, the Key Laboratory for Reproductive Medicine of Guangdong Province, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Jun BianDepartment of Urology, the Third Affiliated Hospital of Southern Medical University, Guangzhou, People's Republic of China.
Yanping HuangShanghai Institute of Andrology, Renji Hospital Affiliated Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
Yadong ZhangDepartment of Urology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Zi WanDepartment of Urology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Bin YangDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai, People's Republic of China; Wake Forest Institute of Regenerative Medicine, Wake Forest University, Winston Salem, North Carolina, United States of America.
Haipeng XiaoDepartment of endocrinology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Zhou SongyangKey Laboratory of Gene Engineering of Ministry of Education, School of Life Sciences, Sun Yat-sen University, Guangzhou, People's Republic of China; State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, People's Republic of China; Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas, United States of America.
Guihua LiuDepartment of Andrology, Center for Reproductive Medicine, the Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China; Wake Forest Institute of Regenerative Medicine, Wake Forest University, Winston Salem, North Carolina, United States of America.
Yuanyuan ZhangWake Forest Institute of Regenerative Medicine, Wake Forest University, Winston Salem, North Carolina, United States of America.
Chunhua DengDepartment of Urology, the First Affiliated Hospital of Sun Yat-sen University, Guangzhou, People's Republic of China.
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CNWake Forest University · USShanghai Jiao Tong University · CNThird Affiliated Hospital of Southern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimThe aim of this study was to determine the possibility of improving erectile dysfunction using cell therapy with either human urine-derived stem cells (USCs) or USCs genetically-modified with FGF2 in a type 2 diabetic rat model.

methodsHuman USCs were collected from 3 healthy donors. USCs were transfected with FGF2 (USCs-FGF2). Sixty-five SD male rats were divided into five groups (G). A control group of normal rats (G1, n = 10), and four other test groups of type 2 diabetic erectile dysfunction rats: PBS as a negative control (G2, n = 10), USCs (G3, n = 15), lentivirus-FGF2 (G4, n = 15), and USCs-FGF2 (G5, n = 15). Diabetes was induced in the rats via a high fat diet for 28 days and a subsequent intraperitoneal injection of streptozotocin (35 mg/kg). Erectile dysfunction was screened with apomorphine (100 μg/kg). Cell injections in the test groups (G2-G5) occurred directly into the corpora cavernosa. The implanted cells were tracked at 7 days (n = 5 animals/G) and 28 days (n = 10 animals/G) post injection. Mean arterial pressure (MAP), intracavernosal pressure (ICP), expression of endothelial markers (CD31, VEGF and eNOS), smooth muscle markers (desmin and smoothelin), histological changes and erectile function were assessed for each group.

resultsUSCs expressed mesenchymal stem cell markers, and secreted a number of proangiogenic growth factors. USCs expressed endothelial cell markers (CD31 and vWF) after transfection with FGF2. Implanted USCs or USCs-FGF2 displayed a significantly raised ICP and ICP/MAP ratio (p<0.01) 28 days after intracavernous injection. Although few cell were detected within the implanted sites, histological and western blot analysis demonstrated an increased expression of endothelial and smooth muscle markers within the cavernous tissue following USC or USC-FGF2 injection.

conclusionsThe paracrine effect of USCs or USCs-FGF2 induced improvement of erectile function in type 2 diabetic rats by recruiting resident cells and increasing the endothelial expression and contents of smooth muscle.

Indexed as

Diabetes ComplicationsDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Erectile DysfunctionFibroblast Growth Factor 2Stem CellsStem Cell TransplantationTransduction, GeneticAdultAnimalsHeterograftsHumansMaleRatsRats, Sprague-DawleyFibroblast Growth Factor 2

Identifiers

PMID24663037
PMCPMC3963968
OpenAlexW2064070589

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.