Evidence map›Paper›PMID 35842645›Full record

ArticleBMC complementary medicine and therapies2022

Identification of core genes associated with the anti-atherosclerotic effects of Salvianolic acid B and immune cell infiltration characteristics using bioinformatics analysis.

Zheng Jin, Huanyi Zhao, Yuan Luo, Xiushen Li, Jiayan Cui, Jing Yan, Pingzhen Yang

Open access · goldAbstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  8. Salvianolic acid B fromFrontiers in pharmacology · 2022
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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

7 authors at 5 institutions in 1 country.

Zheng JinZhuJiang Hospital of Southern Medical University, Guangzhou, 510285, Guangdong, China.
Huanyi ZhaoFirst Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510405, Guangdong, China.
Yuan LuoGuangzhou University of Chinese Medicine, Guangzhou, 510405, Guangdong, China.
Xiushen LiDepartment of Obstetrics and Gynecology, Shenzhen University General Hospital, Shenzhen, China.
Jiayan CuiZhuJiang Hospital of Southern Medical University, Guangzhou, 510285, Guangdong, China.
Jing YanZhuJiang Hospital of Southern Medical University, Guangzhou, 510285, Guangdong, China. yanve1008@126.com.
Pingzhen YangZhuJiang Hospital of Southern Medical University, Guangzhou, 510285, Guangdong, China. y_pingzhen@126.com.
Southern Medical University · CNZhujiang Hospital · CNFirst Affiliated Hospital of Guangzhou University of Chinese Medicine · CNGuangzhou University of Chinese Medicine · CNShenzhen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtherosclerosis (AS) is the greatest contributor to pathogenesis of atherosclerotic cardiovascular disease (ASCVD), which is associated with increased mortality and reduced quality of life. Early intervention to mitigate AS is key to prevention of ASCVD. Salvianolic acid B (Sal B) is mainly extracted from root and rhizome of Salvia Miltiorrhiza Bunge, and exerts anti-atherosclerotic effect. The purpose of this study was to screen for anti-AS targets of Sal B and to characterize immune cell infiltration in AS.

methodsWe identified targets of Sal B using SEA ( http://sea.bkslab.org/ ) and SIB ( https://www.sib.swiss/ ) databases. GSE28829 and GSE43292 datasets were obtained from Gene Expression Omnibus database. We identified differentially expressed genes (DEGs) and performed enrichment analysis. Weighted gene co-expression network analysis (WGCNA) was used to determine the most relevant module associated with atherosclerotic plaque stability. Intersecting candidate genes were evaluated by generating receiver operating characteristic (ROC) curves and molecular docking. Then, immune cell types were identified using CIBERSOFT and single-sample gene set enrichment analysis (ssGSEA), the relationship between candidate genes and immune cell infiltration was evaluated. Finally, a network-based approach to explore the candidate genes relationship with microRNAs (miRNAs) and Transcription factors (TFs).

resultsMMP9 and MMP12 were been selected as candidate genes from 64 Sal B-related genes, 81 DEGs and turquoise module with 220 genes. ROC curve results showed that MMP9 (AUC = 0.815, P<0.001) and MMP12 (AUC = 0.763, P<0.001) were positively associated with advanced atherosclerotic plaques. The results of immune infiltration showed that B cells naive, B cells memory, Plasma cells, T cells CD8, T cells CD4 memory resting, T cells CD4 memory activated, T cells regulatory (Tregs), T cells gamma delta, NK cells activated, Monocytes, and Macrophages M0 may be involved in development of AS, and the candidate genes MMP9 and MMP12 were associated with these immune cells to different degrees. What' s more, miR-34a-5p and FOXC1, JUN maybe the most important miRNA and TFs.

conclusionThe anti-AS effects of Sal B may be related to MMP9 and MMP12 and associated with immune cell infiltration, which is expected to be used in the early intervention of AS.

Indexed as

AtherosclerosisMicroRNAsPlaque, AtheroscleroticBenzofuransComputational BiologyDepsidesGene Expression ProfilingGene Regulatory NetworksHumansMatrix Metalloproteinase 12Matrix Metalloproteinase 9Molecular Docking SimulationProtein Interaction MapsQuality of LifeBenzofuransDepsidesMatrix Metalloproteinase 12Matrix Metalloproteinase 9MicroRNAssalvianolic acid BAtherosclerosisBioinformatic analysisImmune cell infiltrationSalvianolic acid B

Identifiers

PMID35842645
PMCPMC9288713
OpenAlexW4285587492

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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.