Evidence map›Paper›PMID 34790800›Full record

ArticleAnnals of translational medicine2021

MiR-139-5p has an antidepressant-like effect by targeting phosphodiesterase 4D to activate the cAMP/PKA/CREB signaling pathway.

Peng Huang, Songren Wei, Meng Luo, Zhuohong Tang, Qingmei Lin, Xing Wang, Mi Luo, Yanjun He, Chuan Wang, Dezhan Wei and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  5. Review
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  7. Article
  8. The role of microRNAs in depression.Frontiers in pharmacology · 2023
    Review
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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

12 authors at 4 institutions in 1 country.

Peng Huang *South Medical University Affiliated Maternal & Child Health Hospital of Foshan, Foshan, China.
Songren Wei *Department of Neuropharmacology and Novel Drug Discovery, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Meng LuoCenter for Bioinformatics, School of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Zhuohong TangSouth Medical University Affiliated Maternal & Child Health Hospital of Foshan, Foshan, China.
Qingmei LinSouth Medical University Affiliated Maternal & Child Health Hospital of Foshan, Foshan, China.
Xing WangSouth Medical University Affiliated Maternal & Child Health Hospital of Foshan, Foshan, China.
Mi LuoSouth Medical University Affiliated Maternal & Child Health Hospital of Foshan, Foshan, China.
Yanjun HeSouth Medical University Affiliated Maternal & Child Health Hospital of Foshan, Foshan, China.
Chuan WangDepartment of Biliary Surgery, The First People's Hospital of Foshan, Foshan, China.
Dezhan WeiSouth Medical University Affiliated Maternal & Child Health Hospital of Foshan, Foshan, China.
Chenglai XiaSouth Medical University Affiliated Maternal & Child Health Hospital of Foshan, Foshan, China.
Jiangping XuDepartment of Neuropharmacology and Novel Drug Discovery, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Foshan Maternity and Child Health Care Hospital · CNSouthern Medical University · CNFirst People's Hospital of Foshan · CNHarbin Institute of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhosphodiesterase 4D (PDE4D) inhibitor is commonly used to treat depression, but side effects seriously decrease its efficacy. PDE4D was a downstream target mRNA of miR-139-5p. Therefore, we examined the effects of hippocampal miR-139-5p gain- and loss-of-function on depression-like behaviors, the expression level of PDE4D, and hippocampus neurogenesis.

methodsBioinformatic analyses were carried out to to screen differential genes. Quantitative real-time polymerase chain reaction (qRT-PCR) and luciferase reporter assay were used to confirm the relationship between miR-139-5p and PDE4D. MiR-139-5p mimics, miR-139-5p inhibitor, or miR-NC were used to explore the function of miR-139-5p in HT-22 cells. We further explored the role of miR-139-5p

resultsHere, we showed that PDE4D messenger RNA (mRNA) was a direct target of microRNA (miR)-139-5p, which was downregulated in a chronic ultra-mild stress (CUMS)-induced depression mouse model. Moreover, in experiments

conclusionsOur findings suggested that miR-139-5p acted like an antidepressant by targeting PDE4D, thereby regulating the cAMP/protein kinase A (PKA)/CREB/BDNF pathway to improve depression.

Indexed as

brain-derived neurotrophic factor (BDNF)cyclic adenosine monophosphate (cAMP)DepressionmiR-139-5pphosphodiesterase 4D (PDE4D)

Identifiers

PMID34790800
PMCPMC8576692
OpenAlexW3209870432

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.