Evidence map›Paper›PMID 31653075›Full record

ArticleInternational journal of molecular sciences2019

Dynamic Regulation of miRNA Expression by Functionally Enhanced Placental Mesenchymal Stem Cells PromotesHepatic Regeneration in a Rat Model with Bile Duct Ligation.

Jae Yeon Kim, Ji Hye Jun, Soo Young Park, Seong Wook Yang, Si Hyun Bae, Gi Jin Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

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  13. Application of Perinatal Derivatives in Ovarian Diseases.Frontiers in bioengineering and biotechnology · 2022
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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

6 authors at 3 institutions in 1 country.

Jae Yeon KimDepartment of Biomedical Science, CHA University, Seongnam 13488, Korea. janejykim92@gmail.com.
Ji Hye JunDepartment of Biomedical Science, CHA University, Seongnam 13488, Korea. jihyejun1015@gmail.com.
Soo Young ParkDepartment of Biomedical Science, CHA University, Seongnam 13488, Korea. soobookpark@gmail.com.
Seong Wook YangDepartment of Systems Biology, College of Life Science and Biotechnology, Yonsei University, Seoul 120749, Korea. yangsw@yonsei.ac.kr.
Si Hyun BaeDepartment of Internal Medicine, Catholic University Medical College, Seoul 03312, Korea. baesh@catholic.ac.kr.
Gi Jin KimDepartment of Biomedical Science, CHA University, Seongnam 13488, Korea. gjkim@cha.ac.kr.
CHA University · KRCatholic University of Korea · KRYonsei University · KR

Funding

Korea Health Industry Development Institute HI17C1050
6 · The paper itself

Abstract

Placenta-derived mesenchymal stem cells (PD-MSCs) were highlighted as therapeutic sources in several degenerative diseases. Recently, microRNAs (miRNAs)were found to mediate one of the therapeutic mechanisms of PD-MSCs in regenerative medicine. To enhance the therapeutic effects of PD-MSCs, we established functionally enhanced PD-MSCs with phosphatase of regenerating liver-1 overexpression (PRL-1(+)). However, the profile and functions of miRNAs induced by PRL-1(+) PD-MSCs in a rat model with hepatic failure prepared by bile duct ligation (BDL) remained unclear. Hence, the objectives of the present study were to analyze the expression of miRNAs and investigate their therapeutic mechanisms for hepatic regeneration via PRL-1(+) in a rat model with BDL. We selected candidate miRNAs based on microarray analysis. Under hypoxic conditions, compared with migrated naïve PD-MSCs, migrated PRL-1(+) PD-MSCs showed improved integrin-dependent migration abilitythrough Ras homolog (RHO) family-targeted miRNA expression (e.g., hsa-miR-30a-5p, 340-5p, and 146a-3p). Moreover, rno-miR-30a-5p and 340-5p regulated engraftment into injured rat liver by transplantedPRL-1(+) PD-MSCs through the integrin family. Additionally, an increase inplatelet-derived growth factor receptor A (PDGFRA) by suppressing rno-miR-27a-3p improved vascular structure in rat liver tissues after PRL-1(+) PD-MSC transplantation. Furthermore, decreased rno-miR-122-5p was significantly correlated with increased proliferation of hepatocytes in liver tissues by PRL-1(+) PD-MSCs byactivating the interleukin-6 (IL-6) signaling pathway through the repression of rno-miR-21-5p. Taken together, these findings improve the understandingof therapeutic mechanisms based on miRNA-mediated stem-cell therapy in liver diseases.

Indexed as

Mesenchymal Stem Cell TransplantationRegenerationAnimalsCell HypoxiaCells, CulturedDisease Models, AnimalFemaleHumansImmediate-Early ProteinsInterleukin-6LiverLiver FailureMesenchymal Stem CellsMicroRNAsPlacentaPregnancyImmediate-Early ProteinsInterleukin-6MicroRNAsProtein Tyrosine PhosphatasesPtp4a1 protein, ratReceptor, Platelet-Derived Growth Factor alphaLiver failuremicroRNAs (miRNAs)phosphatase of regenerating liver-1 (PRL-1)placenta-derived mesenchymal stem cells (PD-MSCs)regenerative medicinestem-cell homingvascular remodeling

Identifiers

PMID31653075
PMCPMC6862171
OpenAlexW2956029287

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.