Evidence map›Paper›PMID 28761088›Full record

ArticleScientific reports2017

Shift of EMT gradient in 3D spheroid MSCs for activation of mesenchymal niche function.

Sohee Jeon, Ho-Sun Lee, Ga-Young Lee, Gyeongsin Park, Tae-Min Kim, Jihye Shin, Cheolju Lee, Il-Hoan Oh

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

24 citing papers in PubMed, 41 citations in OpenAlex.

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  20. Five Decades Later, Are Mesenchymal Stem Cells Still Relevant?Frontiers in bioengineering and biotechnology · 2020
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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 2 institutions in 1 country.

Sohee JeonCatholic High-Performance Cell Therapy Center, The Catholic University of Korea, College of Medicine, Seoul, 137-701, Korea.
Ho-Sun LeeCatholic High-Performance Cell Therapy Center, The Catholic University of Korea, College of Medicine, Seoul, 137-701, Korea.
Ga-Young LeeCatholic High-Performance Cell Therapy Center, The Catholic University of Korea, College of Medicine, Seoul, 137-701, Korea.
Gyeongsin ParkDepartment of Pathology, Seoul St. Mary's Hospital, The Catholic University of Korea, College of Medicine, Seoul, 137-701, Korea.
Tae-Min KimDepartment of Medical Bioinformatics, The Catholic University of Korea, College of Medicine, Seoul, 137-701, Korea.
Jihye ShinCenter for Theragnosis, Biomedical Research Institute, Korea Institute of Science and Technology, Seoul, 02792, Korea.
Cheolju LeeCenter for Theragnosis, Biomedical Research Institute, Korea Institute of Science and Technology, Seoul, 02792, Korea.
Il-Hoan OhCatholic High-Performance Cell Therapy Center, The Catholic University of Korea, College of Medicine, Seoul, 137-701, Korea. iho@catholic.ac.kr.
Catholic University of Korea · KRKorea Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the wide use of mesenchymal stromal cells (MSCs) for paracrine support in clinical trials, their variable and heterogeneous supporting activity pose major challenges. While three-dimensional (3D) MSC cultures are emerging as alternative approaches, key changes in cellular characteristics during 3D-spheroid formation remain unclear. Here, we show that MSCs in 3D spheroids undergo further progression towards the epithelial-mesenchymal transition (EMT), driven by upregulation of EMT-promoting microRNAs and suppression of EMT-inhibitory miRNAs. The shift of EMT in MSCs is associated with widespread histone modifications mimicking the epigenetic reprogramming towards enhanced chromatin dynamics and stem cell-like properties, but without changes in their surface phenotype. Notably, these molecular shifts towards EMT in 3D MSCs caused enhanced stem cell niche activity, resulting in higher stimulation of hematopoietic progenitor self-renewal and cancer stem cell metastasis. Moreover, miRNA-mediated induction of EMT in 2D MSCs were sufficient to mimic the enhanced niche activity of 3D spheroid MSCs. Thus, the molecular hierarchy in the EMT gradient among phenotypically indistinguishable MSCs revealed the previously unrecognized functional parameters in MSCs, and the EMT-enhanced "naïve" mesenchymal state represents an 'activated mesenchymal niche' in 3D spheroid MSCs.

Indexed as

Epithelial-Mesenchymal TransitionStem Cell NicheAnimalsCell Line, TumorCellular ReprogrammingFemaleHistone CodeHumansHuman Umbilical Vein Endothelial CellsMesenchymal Stem CellsMiceMice, Inbred NODMice, SCIDMicroRNAsSpheroids, CellularMicroRNAs

Identifiers

PMID28761088
PMCPMC5537359
OpenAlexW2737265510

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.