Evidence map›Paper›PMID 35139764›Full record

ArticleBioengineered2022

Improving the repair mechanism and miRNA expression profile of tibial defect in rats based on silent information regulator 7 protein analysis of mesenchymal stem cells.

Rui Chen, Haizhou Huang, Li Liang, Weibin Zhang, Yingjie Zheng, Dehong Fu, Shibang Lin

Abstract read
In one paragraph

Article in Bioengineered, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Rui Chen
Haizhou Huang
Li LiangOrthopaedic Trauma, Maoming People's Hospital, Maoming City, China.
Weibin ZhangOrthopaedic Trauma, Maoming People's Hospital, Maoming City, China.
Yingjie ZhengOrthopaedic Trauma, Maoming People's Hospital, Maoming City, China.
Dehong FuOrthopaedic Trauma, Maoming People's Hospital, Maoming City, China.
Shibang LinOrthopaedic Trauma, Maoming People's Hospital, Maoming City, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to verify the role of Silent Information Regulator 7 (SIRT7) in improving the repair mechanism of bone marrow mesenchymal stem cells (BMMSCs) and the expression of microribonucleic acid (miRNA). Human BMMSCs were extracted from patients with femoral fractures, and the proliferation activity of human BMMSCs before and after knockout SIRT7 and the expression levels of bone-related genes and proteins were compared. Thirty-two 8-week-old male Sprague-Dawley (SD) rats were randomly divided into a blank group, a chitosan scaffold group, a control group, and a silence information regulator knockout group 7 (n = 8). In addition to the blank group, the chitosan scaffold, the green fluorescent protein (GFP) transfected stem cell composite chitosan scaffold, and the SIRT7 knockout stem cell composite chitosan scaffold were implanted in the other three groups, respectively. The X-rays and small animal in vivo three-dimensional tomography (Micro-CT) were adopted to quantitatively analyze the volume fraction, the number of trabeculae, and the connection density. Compared with the other three groups, the bone defect was formed more in the medullary mesenchymal stem cell knockout group, and the bone volume fraction, number of trabeculae and connection density were significantly increased (

Indexed as

ChitosanMesenchymal Stem CellsMicroRNAsAnimalsCells, CulturedHumansMaleRatsRats, Sprague-DawleyTissue EngineeringChitosanMicroRNAsMIRN98 microRNA-98, ratMIRN98 microRNA, humanBMMSCsmiRNASIRT7 proteintibial defecttibial defect model

Identifiers

PMID35139764
PMCPMC8973621

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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.