Evidence map›Paper›PMID 37855249›Full record

ArticleJournal of cellular and molecular medicine2023

Let-7a promotes periodontal bone regeneration of bone marrow mesenchymal stem cell aggregates via the Fas/FasL-autophagy pathway.

Shiyao Yang, Jing Gao, Meng Chen, Yuting Sun, Xin Qiao, Hongchen Mao, Li Guo, Yang Yu, Deqin Yang

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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.

Shiyao YangDepartment of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.
Jing GaoDepartment of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.
Meng ChenDepartment of Oral and Maxillofacial Surgery, Daping Hospital, Army Medical University, Chongqing, China.
Yuting SunDepartment of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.
Xin QiaoDepartment of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.
Hongchen MaoDepartment of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.
Li GuoDepartment of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.
Yang YuDepartment of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.ORCID 0000-0001-8646-8963
Deqin YangDepartment of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.ORCID 0000-0002-2579-8384

Funding

National Natural Science Foundation of China 31970783National Natural Science Foundation of China 32270888National Natural Science Foundation of China 81800979Program for Top talent Distinguished Professor from Chongqing Medical University [2021] 215Program for Youth Innovation in Future Medicine from Chongqing Medical University W0060
6 · The paper itself

Abstract

Periodontal bone regeneration using bone marrow mesenchymal stem cell (BMMSC) transplantation is a promising method; however, the method for osteogenic differentiation of BMMSCs needs to be improved. In this research, we sought to identify the roles of let-7a in the osteogenesis of BMMSCs and to provide a potential method for periodontal bone regeneration. Our previous study revealed that Fas/FasL is a target of let-7a. In this study, we demonstrated that let-7a overexpression significantly enhanced BMMSC-CAs osteogenesis both in vitro and in vivo. Mechanistically, upregulation of Fas/FasL using the rfas/rfaslg plasmid obstructed the osteogenesis of BMMSCs by inhibiting autophagy. Furthermore, we confirmed that overexpression of let-7a activated autophagy and alleviated the inhibited osteogenesis by the autophagy inhibitor 3-MA and the rfas/rfaslg plasmid of BMMSCs. In general, our findings showed that let-7a promoted the osteogenesis of BMMSCs through the Fas/FasL-autophagy pathway, suggesting that the application of let-7a in BMMSC-CAs based periodontal bone regeneration could be a promising strategy.

Indexed as

Bone RegenerationMesenchymal Stem CellsMicroRNAsOsteogenesisAnimalsAutophagyBone Marrow CellsCell DifferentiationCells, CulturedFas Ligand Proteinfas ReceptorRatsUp-RegulationFaslg protein, ratFas Ligand ProteinFas protein, ratfas ReceptorMicroRNAsmirnlet7 microRNA, mouseMIRNLET7 microRNA, ratBMMSCscell-aggregatesFas/FasLmicroRNAperiodontal regeneration

Identifiers

PMID37855249
PMCPMC10746947

What OpenQuestion holds

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Registered trials

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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.