Evidence map›Paper›PMID 27829839›Full record

ReviewStem cells international2016

Therapeutic Potential of Stem Cells Strategy for Cardiovascular Diseases.

Chang Youn Lee, Ran Kim, Onju Ham, Jihyun Lee, Pilseog Kim, Seokyeon Lee, Sekyung Oh, Hojin Lee, Minyoung Lee, Jongmin Kim and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Stem cells international, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Regenerative Therapy for Cardiomyopathies.Journal of cardiovascular translational research · 2018
    Review
  12. Article
  13. Review
  14. Article
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

11 authors at 7 institutions in 2 countries.

Chang Youn LeeDepartment of Integrated Omics for Biomedical Sciences, Graduate School, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-759, Republic of Korea.
Ran KimDepartment of Biology Education, College of Education, Pusan National University, Busan 609-735, Republic of Korea.ORCID 0000-0001-5048-5235
Onju HamInstitute for Bio-Medical Convergence, Catholic Kwandong University International St. Mary's Hospital, Incheon 404-834, Republic of Korea.ORCID 0000-0003-3910-7211
Jihyun LeeDepartment of Biology Education, College of Education, Pusan National University, Busan 609-735, Republic of Korea.
Pilseog KimDepartment of Biology Education, College of Education, Pusan National University, Busan 609-735, Republic of Korea.ORCID 0000-0003-4653-5230
Seokyeon LeeDepartment of Biology Education, College of Education, Pusan National University, Busan 609-735, Republic of Korea.ORCID 0000-0002-5460-1747
Sekyung OhDepartment of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA.
Hojin LeeDepartment of Pharmacology, Yale University School of Medicine, New Haven, CT 06520, USA.
Minyoung LeeDepartment of Molecular Physiology, College of Pharmacy, Kyungpook National University, Daegu 702-701, Republic of Korea.
Jongmin KimDepartment of Life Systems, Sookmyung Women's University, 52 Hyochangwon-gil, Yongsan-gu, Seoul 140-742, Republic of Korea.
Woochul ChangDepartment of Biology Education, College of Education, Pusan National University, Busan 609-735, Republic of Korea.ORCID 0000-0001-7367-2586
Pusan National University · KRCatholic Kwandong University International St. Mary's Hospital · KRKyungpook National University · KRSookmyung Women's University · KRStanford University · USYale University · USYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite development of medicine, cardiovascular diseases (CVDs) are still the leading cause of mortality and morbidity worldwide. Over the past 10 years, various stem cells have been utilized in therapeutic strategies for the treatment of CVDs. CVDs are characterized by a broad range of pathological reactions including inflammation, necrosis, hyperplasia, and hypertrophy. However, the causes of CVDs are still unclear. While there is a limit to the currently available target-dependent treatments, the therapeutic potential of stem cells is very attractive for the treatment of CVDs because of their paracrine effects, anti-inflammatory activity, and immunomodulatory capacity. Various studies have recently reported increased therapeutic potential of transplantation of microRNA- (miRNA-) overexpressing stem cells or small-molecule-treated cells. In addition to treatment with drugs or overexpressed miRNA in stem cells, stem cell-derived extracellular vesicles also have therapeutic potential because they can deliver the stem cell-specific RNA and protein into the host cell, thereby improving cell viability. Here, we reported the state of stem cell-based therapy for the treatment of CVDs and the potential for cell-free based therapy.

Identifiers

PMID27829839
PMCPMC5088322
OpenAlexW2536181362

What Socratic holds

Textmetadata
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 Socratic graph.