Evidence map›Paper›PMID 36099417›Full record

ArticleNucleic acids research2022

A toolkit for the identification of NEAT1_2/paraspeckle modulators.

Haiyan An, Karen T Elvers, Jason A Gillespie, Kimberley Jones, John R Atack, Olivera Grubisha, Tatyana A Shelkovnikova

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. RNA Triple Helices: From Structures and Mechanisms to Therapeutic Targets.International journal of biological sciences · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Article
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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

7 authors at 1 institution in 1 country.

Haiyan AnMedicines Discovery Institute, School of Biosciences, Cardiff University, Cardiff CF10 3AT, UK.
Karen T ElversMedicines Discovery Institute, School of Biosciences, Cardiff University, Cardiff CF10 3AT, UK.
Jason A GillespieMedicines Discovery Institute, School of Biosciences, Cardiff University, Cardiff CF10 3AT, UK.
Kimberley JonesMedicines Discovery Institute, School of Biosciences, Cardiff University, Cardiff CF10 3AT, UK.
John R AtackMedicines Discovery Institute, School of Biosciences, Cardiff University, Cardiff CF10 3AT, UK.
Olivera GrubishaMedicines Discovery Institute, School of Biosciences, Cardiff University, Cardiff CF10 3AT, UK.
Tatyana A ShelkovnikovaMedicines Discovery Institute, School of Biosciences, Cardiff University, Cardiff CF10 3AT, UK.ORCID 0000-0003-1367-5309
Cardiff University · GB

Funding

Biotechnology and Biological Sciences Research CouncilMotor Neurone Disease Association SHELKOVNIKOVA/OCT17/968-799MRF_ MRF-060-0001-RG-SHELK
6 · The paper itself

Abstract

Paraspeckles are ribonucleoprotein granules assembled by NEAT1_2 lncRNA, an isoform of Nuclear Paraspeckle Assembly Transcript 1 (NEAT1). Dysregulation of NEAT1_2/paraspeckles has been linked to multiple human diseases making them an attractive drug target. However currently NEAT1_2/paraspeckle-focused translational research and drug discovery are hindered by a limited toolkit. To fill this gap, we developed and validated a set of tools for the identification of NEAT1_2 binders and modulators comprised of biochemical and cell-based assays. The NEAT1_2 triple helix stability element was utilized as the target in the biochemical assays, and the cellular assay ('ParaQuant') was based on high-content imaging of NEAT1_2 in fixed cells. As a proof of principle, these assays were used to screen a 1,200-compound FDA-approved drug library and a 170-compound kinase inhibitor library and to confirm the screening hits. The assays are simple to establish, use only commercially-available reagents and are scalable for higher throughput. In particular, ParaQuant is a cost-efficient assay suitable for any cells growing in adherent culture and amenable to multiplexing. Using ParaQuant, we identified dual PI3K/mTOR inhibitors as potent negative modulators of paraspeckles. The tools we describe herein should boost paraspeckle studies and help guide the search, validation and optimization of NEAT1_2/paraspeckle-targeted small molecules.

Indexed as

Cell NucleusParaspecklesRNA, Long NoncodingDrug DiscoveryHumansProtein Kinase InhibitorsNEAT1 long non-coding RNA, humanProtein Kinase InhibitorsRNA, Long Noncoding

Identifiers

PMID36099417
PMCPMC9723620
OpenAlexW4295758346

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.