Evidence map›Paper›PMID 30896075›Full record

ArticleCell proliferation2019

Single cell-derived clonally expanded mesenchymal progenitor cells from somatic cell nuclear transfer-derived pluripotent stem cells ameliorate the endometrial function in the uterus of a murine model with Asherman's syndrome.

Sung-Min Jun, Mira Park, Ji Yoon Lee, Sookyung Jung, Jeoung Eun Lee, Sung Han Shim, Haengseok Song, Dong Ryul Lee

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  15. An update on stem cell therapy for Asherman syndrome.Journal of assisted reproduction and genetics · 2020
    Review
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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

8 authors at 1 institution in 1 country.

Sung-Min JunCHA Advanced Research Institute, Seongnam, Korea.
Mira ParkDepartment of Biomedical Science, CHA University, Seongnam, Korea.
Ji Yoon LeeDepartment of Biomedical Science, CHA University, Seongnam, Korea.
Sookyung JungCHA Advanced Research Institute, Seongnam, Korea.
Jeoung Eun LeeCHA Advanced Research Institute, Seongnam, Korea.
Sung Han ShimDepartment of Biomedical Science, CHA University, Seongnam, Korea.
Haengseok SongDepartment of Biomedical Science, CHA University, Seongnam, Korea.
Dong Ryul LeeCHA Advanced Research Institute, Seongnam, Korea.ORCID http://orcid.org/0000-0003-1534-4810
CHA University · KR

Funding

NRF of Republic of Korea 2015M3A9C6028961NRF of Republic of Korea 2017M3A9C6061284NRF of Republic of Korea 2017M3A9F8072235
6 · The paper itself

Abstract

objectivesBecause primary mesenchymal progenitor cells (adult-MPCs) have various functions that depend on the tissue origin and donor, de novo MPCs from human pluripotent stem cells (hPSCs) would be required in regenerative medicine. However, the characteristics and function of MPCs derived from reprogrammed hPSCs have not been well studied. Thus, we show that functional MPCs can be successfully established from a single cell-derived clonal expansion following MPC derivation from somatic cell nuclear transfer-derived (SCNT)-hPSCs, and these cells can serve as therapeutic contributors in an animal model of Asherman's syndrome (AS). MATERIALS AND

methodsWe developed single cell-derived clonal expansion following MPC derivation from SCNT-hPSCs to offer a pure population and a higher biological activity. Additionally, we investigated the therapeutic effects of SCNT-hPSC-MPCs in model mice of Asherman's syndrome (AS), which is characterized by synechiae or fibrosis with endometrial injury.

resultsTheir humoral effects in proliferating host cells encouraged angiogenesis and decreased pro-inflammatory factors via a host-dependent mechanism, resulting in reduction in AS. We also addressed that cellular activities such as the cell proliferation and population doubling of SCNT-hPSC-MPCs resemble those of human embryonic stem cell-derived MPCs (hESC-MPCs) and are much higher than those of adult-MPCs.

conclusionsSomatic cell nuclear transfer-derived-hPSCs-MPCs could be an advanced therapeutic strategy for specific diseases in the field of regenerative medicine.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsCell DifferentiationCell ProliferationCellular Reprogramming TechniquesClone CellsDisease Models, AnimalEndometriumFemaleGynatresiaHumansMiceMice, Inbred ICRNeovascularization, PhysiologicNuclear Transfer TechniquesPluripotent Stem CellsangiogenesisAsherman’s Syndromehuman pluripotent stem cellsmesenchymal progenitor cellssomatic cell nuclear transfer

Identifiers

PMID30896075
PMCPMC6536448
OpenAlexW2922796664

What OpenQuestion 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 OpenQuestion graph.