Evidence map›Paper›PMID 37779148›Full record

ArticleExperimental & molecular medicine2023

Vascular regeneration and skeletal muscle repair induced by long-term exposure to SDF-1α derived from engineered mesenchymal stem cells after hindlimb ischemia.

Jin-Ju Kim, Jae-Hyun Park, Hyeok Kim, Woo-Sup Sim, Seokbeom Hong, Yeon-Jik Choi, Hyo-Jin Kim, Soon Min Lee, Dongha Kim, Sun-Woong Kang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Experimental & molecular medicine, 2023. 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
2.6field-weighted citation impact, top 10% 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, 9 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

Jin-Ju KimDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, Seoul, South Korea.ORCID http://orcid.org/0000-0001-8535-4964
Jae-Hyun ParkDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, Seoul, South Korea.
Hyeok KimDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, Seoul, South Korea.ORCID http://orcid.org/0000-0001-9184-5882
Woo-Sup SimDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, Seoul, South Korea.
Seokbeom HongDepartment of Thoracic and Cardiovascular Surgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Yeon-Jik ChoiDivision of Cardiology, Department of Internal Medicine, Eunpyeong St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Hyo-Jin KimSL BIGEN, Inc., Kyonggi-do, South Korea.
Soon Min LeeSL BIGEN, Inc., Kyonggi-do, South Korea.
Dongha KimDepartment of Anatomy, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Sun-Woong KangResearch Group for Biomimetic Advanced Technology, Korea Institute of Toxicology 7 (KIT), Daejeon, South Korea.ORCID http://orcid.org/0000-0001-8862-2151
Kiwon BanDepartment of Biomedical Sciences, City University of Hong Kong, Kowloon Tong, Hong Kong. kiwonban@cityu.edu.hk.ORCID http://orcid.org/0000-0003-0805-5439
Hun-Jun ParkDepartment of Biomedicine & Health Sciences, The Catholic University of Korea, Seoul, South Korea. cardioman@catholic.ac.kr.ORCID http://orcid.org/0000-0001-8009-9546
The Catholic University of Korea Seoul St. Mary's Hospital · KRCatholic University of Korea · KRCity University of Hong Kong · HKKorea Institute of Toxicology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite recent progress in medical and endovascular therapy, the prognosis for patients with critical limb ischemia (CLI) remains poor. In response, various stem cells and growth factors have been assessed for use in therapeutic neovascularization and limb salvage in CLI patients. However, the clinical outcomes of cell-based therapeutic angiogenesis have not provided the promised benefits, reinforcing the need for novel cell-based therapeutic angiogenic strategies to cure untreatable CLI. In the present study, we investigated genetically engineered mesenchymal stem cells (MSCs) derived from human bone marrow that continuously secrete stromal-derived factor-1α (SDF1α-eMSCs) and demonstrated that intramuscular injection of SDF1α-eMSCs can provide long-term paracrine effects in limb ischemia and effectively contribute to vascular regeneration as well as skeletal muscle repair through increased phosphorylation of ERK and Akt within the SDF1α/CXCR4 axis. These results provide compelling evidence that genetically engineered MSCs with SDF-1α can be an effective strategy for successful limb salvage in limb ischemia.

Indexed as

Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationAnimalsChemokine CXCL12HindlimbHumansIschemiaMuscle, SkeletalNeovascularization, PhysiologicChemokine CXCL12

Identifiers

PMID37779148
PMCPMC10618463
OpenAlexW4387229820

What OpenQuestion holds

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LicenceCC BY
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.