Evidence map›Paper›PMID 30589396›Full record

ArticleCell cycle (Georgetown, Tex.)2018

MiR-221 is involved in depression by regulating Wnt2/CREB/BDNF axis in hippocampal neurons.

Nan Lian, Qihui Niu, Yang Lei, Xue Li, Youhui Li, Xueqin Song

Registry-linked trialAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04998097 (Changes in Serum miRNA and BDNF Levels in Bipolar II Depression Treated by Theta-burst Stimulation), which is not on this map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 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.

NCT04998097 naunknown statusnot on this mapstarted 2022, after this paper: background citation

Changes in Serum miRNA and BDNF Levels in Bipolar II Depression Treated by Theta-burst Stimulation: A Randomized Sham-controlled Exploratory Study

TypeinterventionalSponsorKaohsiung Veterans General Hospital.Ran2022 to 2024Enrolled60ConditionsBipolar II Disorder, Most Recent Episode Major DepressiveArmsrepetitive transcranial magnetic stimulation (rTMS), sham repetitive transcranial magnetic stimulation (rTMS)
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Role of microRNAs in the pathophysiology of addiction.Wiley interdisciplinary reviews. RNA · 2021
    Pooled it
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  20. MicroRNAs, Multiple Sclerosis, and Depression.International journal of molecular sciences · 2021
    Review
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

6 authors.

Nan Liana Department of Psychiatry , The First Affiliated Hospital of Zhengzhou University , Zhengzhou Henan , China.
Qihui Niua Department of Psychiatry , The First Affiliated Hospital of Zhengzhou University , Zhengzhou Henan , China.
Yang Leia Department of Psychiatry , The First Affiliated Hospital of Zhengzhou University , Zhengzhou Henan , China.
Xue Lia Department of Psychiatry , The First Affiliated Hospital of Zhengzhou University , Zhengzhou Henan , China.
Youhui Lia Department of Psychiatry , The First Affiliated Hospital of Zhengzhou University , Zhengzhou Henan , China.
Xueqin Songa Department of Psychiatry , The First Affiliated Hospital of Zhengzhou University , Zhengzhou Henan , China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study was to investigate the mechanism of miR-221 in depression.

methodsThe molecules expressions were measured by qRT-PCR and western blot. The sucrose preference test (SPT), forced swimming test (FST) and tail suspension test (TST) were used to detect depressive-like symptoms. MTT assay and flow cytometric was used to measure the proliferation and apoptosis of hippocampal neuronal.

resultsMiR-221 expression in the cerebrospinal fluid and serum of major depressive disorder patients and the hippocampus of chronic unpredictable mild stress (CUMS) mice were increased, while the expression of Wnt2, p-CREB and BDNF were decreased. Additionally, silence of miR-221 increased sucrose preference of CUMS mice and shortened the immobility time of CUMS mice in SPT and FST. MiR-221 could targeted regulate Wnt2, and knockdown of Wnt2 reversed the effect of miR-221 inhibitor on the proliferation and apoptosis of hippocampal neurons and countered the promoting effect of miR-221 inhibitor on the expression of Wnt2, p-CREB and BDNF.

conclusionMiR-221 could promote the development of depression by regulating Wnt2/CREB/BDNF axis.

Indexed as

AdultAnimalsAntagomirsApoptosisBrain-Derived Neurotrophic FactorCase-Control StudiesCREB-Binding ProteinFemaleHumansMajor Depressive DisorderMaleMiceMice, Inbred C57BLMicroRNAsNeuronsRNA InterferenceAntagomirsBrain-Derived Neurotrophic FactorCREB-Binding ProteinMicroRNAsMIRN221 microRNA, mouseRNA, Small InterferingWnt2 ProteinMajor depressive disordermiR-221Wnt2/CREB/BDNF

Identifiers

PMID30589396
PMCPMC6343714

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.