Evidence map›Paper›PMID 38833209›Full record

ArticleIn vitro cellular & developmental biology. Animal2024

MiR-483-3p promotes dental pulp stem cells osteogenic differentiation via the MAPK signaling pathway by targeting ARRB2.

Xin Yu, Juan Ge, Huimin Xie, Jialu Qian, Wenqian Xia, Qinghua Wang, Xiaorong Zhou, Yan Zhou

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. 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

8 authors.

Xin Yu *Department of Orthodontics and Periodontology, Affiliated Nantong Stomatological Hospital of Nantong University, 36 South Yuelong Road, Nantong, 226001, China.ORCID http://orcid.org/0000-0002-0818-994X
Juan Ge *Department of Immunology, School of Medicine, Nantong University, Nantong, China.
Huimin XieDepartment of Orthodontics and Periodontology, Affiliated Nantong Stomatological Hospital of Nantong University, 36 South Yuelong Road, Nantong, 226001, China.
Jialu QianDepartment of Clinical Laboratory, The First People's Hospital of Nantong, The Second Affiliated Hospital of Nantong University, Nantong, China.
Wenqian XiaDepartment of Orthodontics and Periodontology, Affiliated Nantong Stomatological Hospital of Nantong University, 36 South Yuelong Road, Nantong, 226001, China.
Qinghua WangLaboratory Animal Center, Nantong University, Nantong, China.
Xiaorong ZhouDepartment of Immunology, School of Medicine, Nantong University, Nantong, China. zhouxiaorong@ntu.edu.cn.
Yan ZhouDepartment of Orthodontics and Periodontology, Affiliated Nantong Stomatological Hospital of Nantong University, 36 South Yuelong Road, Nantong, 226001, China. ntyaner@126.com.

Funding

Nantong Basic Science Research Program JC22022099Nantong University Clinical Medicine Special Project 2022JQ007Nantong University Clinical Medicine Special Project 2023JQ003Science and Technology Project of Nantong City MSZ2023002State Key Laboratory of Oral Disease JSKLOD-KF-2101the Fifth Orthodontic Committee of Jiangsu Stomatological Association Joa-2022-6
6 · The paper itself

Abstract

Human dental pulp stem cells (DPSCs) have become an important component for bone tissue engineering and regenerative medicine due to their ability to differentiate into osteoblast precursors. Two miRNA chip datasets (GSE138180 and E-MTAB-3077) of DPSCs osteogenic differentiation were analyzed respectively to find the expression of miR-483-3p significantly increased in the differentiated groups. We further confirmed that miR-483-3p continued to overexpress during osteogenic differentiation of DPSCs, especially reaching its peak on the 7th day. Moreover, miR-483-3p could significantly promote the expression of osteogenic markers including RUNX2 and OSX, and activate MAPK signaling pathway by inducing phosphorylation of ERK, p38, and JNK. In addition, as a significant gene within the MAPK signaling pathway, ARRB2 was identified as the target gene of miR-483-3p by bioinformatic prediction and experimental verification. In conclusion, we identified miR-483-3p could promote osteogenic differentiation of DPSCs via the MAPK signaling pathway by targeting ARRB2.

Indexed as

Cell DifferentiationDental PulpMAP Kinase Signaling SystemMicroRNAsOsteogenesisStem CellsBase SequenceHumansMicroRNAsMIRN483 microRNA, humanARRB2DPSCsMAPK pathwaymiR-483-3pOsteogenic differentiation

Identifiers

What Socratic 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 Socratic graph.