Evidence map›Paper›PMID 29249185›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2018

MiR-145 regulates osteogenic differentiation of human adipose-derived mesenchymal stem cells through targeting FoxO1.

Wei Hao, Hongzhi Liu, Lugang Zhou, Yujie Sun, Hao Su, Jianqiang Ni, Tian He, Peng Shi, Xin Wang

Open access · bronzeAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 40 citations in OpenAlex.

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  6. Bone marrow stromal cells (BMSCs CD45Journal of cellular and molecular medicine · 2021
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  8. Molecular medicine reports · 2021
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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

9 authors at 1 institution in 1 country.

Wei HaoDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.
Hongzhi LiuDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.
Lugang ZhouDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.
Yujie SunDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.
Hao SuDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.
Jianqiang NiDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.
Tian HeDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.
Peng ShiDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.
Xin WangDepartment of Orthopaedics and Traumatology, YanTai YuHuangDing Hospital, Shandong 264000, China.ORCID 0000-0001-9333-4218
Yuhuangding Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we aimed to investigate the expression of miR-145 before and after hASCs osteogenic differentiation. We also intended to explore the influence of the target relationship between miR-145 and FoxO1 on osteogenic differentiation. Dual-luciferase reporter gene assay and real-time PCR were used to confirm the target relationship between miR-145 and FoxO1. Furthermore, the modulatory effects of miR-145 and FoxO1 on hASCs osteoinductive differentiation were measured by real-time PCR , Western blot, ALP staining, ARS staining, and cell immunofluorescence assay. After osteogenic differentiation, miR-145 was gradually down-regulated, while FoxO1 was up-regulated in hASCs. MiR-145 could directly target FoxO1 3'UTR. FoxO1 was negatively regulated by miR-145. After osteoinductive differentiation, BSP, Ocn, and OPN expression was lowered with the overexpression of miR-145 or the knockdown of FoxO1. Furthermore, ALP and ARS staining assay results showed weakened ALP activity and extracellular matrix calcification. When overexpressing miR-145 and FoxO1 simultaneously, no obvious change in ALP activity and extracellular matrix calcification was seen. MiR-145 could suppress hASCs osteoinductive differentiation by suppressing FoxO1 directly. Impact statement Researching on ASCs was a promising strategy to study osteogenic differentiation. The regulatory role of miR-145 on hASCs osteogenic differentiation remained partially explored. Our study revealed a novel mechanism of the osteogenic differentiation process and suggested that miR-145 and its target gene FoxO1 may be potential targets for the therapy of human osteogenic-related disorders.

Indexed as

Cell DifferentiationOsteogenesisBlotting, WesternCells, CulturedFluorescent Antibody TechniqueForkhead Box Protein O1Gene Expression ProfilingGenes, ReporterHumansLuciferasesMesenchymal Stem CellsMicroRNAsReal-Time Polymerase Chain ReactionForkhead Box Protein O1FOXO1 protein, humanLuciferasesMicroRNAsMIRN145 microRNA, humanFoxO1human adipose-derived stem cellsmiR-145osteogenic differentiation

Identifiers

PMID29249185
PMCPMC6022928
OpenAlexW2779482294

What OpenQuestion holds

Textmetadata
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.