Evidence map›Paper›PMID 35499794›Full record

ArticleMolecular neurobiology2022

Hotair and Malat1 Long Noncoding RNAs Regulate Bdnf Expression and Oligodendrocyte Precursor Cell Differentiation.

Fatemeh Khani-Habibabadi, Leila Zare, Mohammad Ali Sahraian, Mohammad Javan, Mehrdad Behmanesh

Abstract read
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Article in Molecular neurobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 19 citations in OpenAlex.

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  12. The multifaceted functions of long non-coding RNAExpert reviews in molecular medicine · 2024
    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

5 authors at 2 institutions in 1 country.

Fatemeh Khani-HabibabadiDepartment of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, P.O. Box: 14115-154, Iran.
Leila ZareDepartment of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, P.O. Box: P.O. Box 14115-331, Iran.
Mohammad Ali SahraianMS Research Center, Neuroscience Institute, Tehran University of Medical Science, Tehran, Iran.
Mohammad JavanDepartment of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, P.O. Box: P.O. Box 14115-331, Iran. mjavan@modares.ac.ir.
Mehrdad BehmaneshDepartment of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, P.O. Box: 14115-154, Iran. behmanesh@modares.ac.ir.ORCID http://orcid.org/0000-0002-3901-304X
Tarbiat Modares University · IRUniversity of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain-derived neurotrophic factor (BDNF) is a member of the neurotrophins family with well-known roles in neural development, differentiation, survival, and synaptic plasticity; however, it has not been explained thoroughly how the expression of this critical gene is regulated. To reveal some aspects of Bdnf gene regulation, here it was explored whether metastasis-associated lung adenocarcinoma transcript 1 (Malat1) and HOX transcript antisense RNA (Hotair) lncRNAs play roles in the regulation of Bdnf expression level, the effect of fingolimod treatment on downstream pathways, and oligodendrocyte precursor cell (OPC) maturation. First, in rat primary glial culture, the effect of Hotair and Malat1 was investigated on Bdnf expression using downregulation by specific DNAzymes. Then, immunostaining and RT-qPCR assays were employed to assess the functions of fingolimod and lncRNAs on OPC maturation. The results demonstrated that Bdnf was significantly correlated to Hotair and Malat1 lncRNAs in glial cells. Also, a strong correlation was observed between these two lncRNAs in glial culture and isolated OPCs. Fingolimod treatment coordinated lncRNAs' role on Bdnf expression in glial cells and enhanced OPC myelination three times compared to control. Furthermore, results suggested that Malat1 may have a role in the last stages of the intrinsic oligodendrocyte (OL) myelination regardless of fingolimod treatment. As BDNF is involved in brain development, survival, and functions, understanding the regulatory mechanism behind BDNF expression leads to a better comprehension of the pathogenesis of the neurodegenerative disorder and designing more effective treatments.

Indexed as

Oligodendrocyte Precursor CellsAnimalsBrain-Derived Neurotrophic FactorFingolimod HydrochlorideOligodendrogliaRatsRNA, Long NoncodingBrain-Derived Neurotrophic FactorFingolimod HydrochlorideHOTAIR long untranslated RNA, ratMALAT1 long noncoding RNA, ratRNA, Long NoncodingBrain-derived neurotrophic factorFingolimodLong noncoding RNAsMyelinOligodendrocyte precursor cells

Identifiers

PMID35499794
OpenAlexW4225284443

What OpenQuestion holds

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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.