Evidence map›Paper›PMID 27716787›Full record

ArticlePloS one2016

Fluoxetine Increases the Expression of miR-572 and miR-663a in Human Neuroblastoma Cell Lines.

Mahesh Mundalil Vasu, Ayyappan Anitha, Taro Takahashi, Ismail Thanseem, Keiko Iwata, Tetsuya Asakawa, Katsuaki Suzuki

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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  5. Review
  6. Article
  7. Article
  8. Article
  9. miRNAs in depression vulnerability and resilience: novel targets for preventive strategies.Journal of neural transmission (Vienna, Austria : 1996) · 2019
    Review
  10. Review
  11. Article
  12. MiR-489 suppresses tumor growth and invasion by targeting HDAC7 in colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2018
    Article
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 2 institutions in 1 country.

Mahesh Mundalil VasuDepartment of Psychiatry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Ayyappan AnithaDepartment of Neurogenetics, Institute for Communicative and Cognitive Neurosciences (ICCONS), Kerala, India.
Taro TakahashiDepartment of Child and Adolescent Psychiatry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Ismail ThanseemDepartment of Neurogenetics, Institute for Communicative and Cognitive Neurosciences (ICCONS), Kerala, India.
Keiko IwataResearch Center for Child Mental Development, University of Fukui, Fukui, Japan.
Tetsuya AsakawaDepartment of Psychiatry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Katsuaki SuzukiDepartment of Biofunctional Imaging, Preeminent Medical Photonics Education and Research Center, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Hamamatsu University School of Medicine · JPUniversity of Fukui · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence suggests neuroprotective effects of fluoxetine, a selective serotonin reuptake inhibitor (SSRI), on the developed neurons in the adult brain. In contrast, the drug may be deleterious to immature or undifferentiated neural cells, although the mechanism is unclear. Recent investigations have suggested that microRNAs (miRNA) may be critical for effectiveness of psychotropic drugs including SSRI. We investigated whether fluoxetine could modulate expressions of neurologically relevant miRNAs in two neuroblastoma SK-N-SH and SH-SY5Y cell lines. Initial screening results revealed that three (miR-489, miR-572 and miR-663a) and four (miR-320a, miR-489, miR-572 and miR-663a) miRNAs were up-regulated in SK-N-SH cells and SH-SY5Y cells, respectively, after 24 hours treatment of fluoxetine (1-25 μM). Cell viability was reduced according to the dose of fluoxetine. The upregulation of miR-572 and miR-663a was consistent in both the SH-SY5Y and SK-N-SH cells, confirmed by a larger scale culture condition. Our data is the first in vitro evidence that fluoxetine could increase the expression of miRNAs in undifferentiated neural cells, and that putative target genes of those miRNAs have been shown to be involved in fundamental neurodevelopmental processes.

Indexed as

Cell DifferentiationCell Line, TumorCell SurvivalFluoxetineGene Expression Regulation, NeoplasticHumansMicroRNAsNeuroblastomaNeurogenesisUp-RegulationFluoxetineMicroRNAsMIRN-572 microRNA, humanMIRN663 microRNA, human

Identifiers

PMID27716787
PMCPMC5055328
OpenAlexW2529259238

What OpenQuestion holds

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LicenceCC BY
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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.