Evidence map›Paper›PMID 35468096›Full record

ArticleAging2022

Effective biomarkers and therapeutic targets of nerve-immunity interaction in the treatment of depression: an integrated investigation of the miRNA-mRNA regulatory networks.

Zixuan Wu, Zhixiang Cai, Hongshuo Shi, Xuyan Huang, Minjie Cai, Kai Yuan, Peidong Huang, Guoqi Shi, Tao Yan, Zhichao Li

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Zixuan WuGuangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong Province, China.
Zhixiang CaiGuangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong Province, China.
Hongshuo ShiShandong University of Traditional Chinese Medicine, Jinan 250355, Shandong Province, China.
Xuyan HuangGuangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong Province, China.
Minjie CaiGuangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong Province, China.
Kai YuanYunnan University of Chinese Medicine, Kunming 650500, Yunnan Province, China.
Peidong HuangYunnan University of Chinese Medicine, Kunming 650500, Yunnan Province, China.
Guoqi ShiGuangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong Province, China.
Tao YanGuangzhou University of Chinese Medicine, Guangzhou 510006, Guangdong Province, China.
Zhichao LiThe Second Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan 250355, Shandong Province, China.
Guangzhou University of Chinese Medicine · CNYunnan University · CNAffiliated Hospital of Shandong University of Traditional Chinese Medicine · CNShandong University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajor depressive disorder (MDD) is an emotional condition that interferes with sufferers' work and daily life. Numerous studies have found that miRNAs play a significant role in the development of MDD and can be utilized as a biomarker for its diagnosis and therapy. However, there have been few studies on nerve-immunity interaction treatment for the brains of MMD patients.

methodsThe work is performed on microarray data. We analyzed the differences of miRNAs (GSE58105, GSE81152, GSE152267, and GSE182194) and mRNA (GSE19738, GSE32280, GSE44593, GSE53987, and GSE98793) in MDD and healthy samples from GEO datasets. FunRich was used to predict the transcription factors and target genes of the miRNAs, and TF and GO enrichment analyses were performed. Then, by comparing the differential expression of the anticipated target genes and five mRNAs, intersecting mRNAs were discovered. The intersecting genes were submitted to GO and KEGG analyses to determine their functions. These intersecting potential genes and pathways that linked to MDD in neurological and immunological aspects have been identified for future investigation.

resultsWe discovered five hub genes: KCND2, MYT1L, GJA1, CHL1, and SNAP25, which were all up-regulated genes. However, in MMD, the equivalent miRNAs, hsa-miR-206 and hsa-miR-338-3p, were both down-regulated. These miRNAs can activate or inhibit the T cell receptor signal pathway, JAK-STAT and other signal pathways, govern immune-inflammatory response, neuronal remodeling, and mediate the onset and development of MMD Conclusions: The results of a thorough bioinformatics investigation of miRNAs and mRNAs in MDD showed that miR-338-3P and miR-206 might be effective biomarkers and possible therapeutic targets for the treatment of MDD via nerve-immunity interaction.

Indexed as

Major Depressive DisorderMicroRNAsBiomarkersComputational BiologyDepressionGene Expression ProfilingGene Regulatory NetworksHumansRNA, MessengerBiomarkersMicroRNAsMIRN206 microRNA, humanMIRN338 microRNA, humanRNA, MessengerbioinformaticsDE-miRNAsmajor depressive disorder (MMD)microRNAs (miRNAs)regulatory networks

Identifiers

PMID35468096
PMCPMC9085226
OpenAlexW4224627783

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LicenceCC BY
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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.