Evidence map›Paper›PMID 35289721›Full record

ArticleRNA biology2022

Genetic tools for the stable overexpression of circular RNAs.

Nicol Mecozzi, Arianna Nenci, Olga Vera, Ilah Bok, Aimee Falzone, Gina M DeNicola, Florian A Karreth

Open access · goldAbstract read
In one paragraph

Article in RNA biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Acta pharmaceutica Sinica. B · 2026
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  7. The therapeutic potential of circular RNAs.Nature reviews. Genetics · 2025
    Review
  8. Article
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  13. Nanoparticles-Delivered Circular RNA Strategy as a Novel Antitumor Approach.International journal of molecular sciences · 2024
    Review
  14. Optimal design of synthetic circular RNAs.Experimental & molecular medicine · 2024
    Review
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  17. 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 3 institutions in 1 country.

Nicol MecozziDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID 0000-0001-6161-5074
Arianna NenciGene Targeting Core Facility, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Olga VeraDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID 0000-0002-1878-4945
Ilah BokDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID 0000-0001-8958-5161
Aimee FalzoneDepartment of Cancer Physiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Gina M DeNicolaDepartment of Cancer Physiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID 0000-0001-6611-6696
Florian A KarrethDepartment of Molecular Oncology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.ORCID 0000-0002-2350-9809
Moffitt Cancer Center · USUniversity of South Florida · USTarget (United States) · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
Investigation of NRF2-Dependent Metabolic LiabilitiesR37CA230042 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI DENICOLA, GINA MARIE · 2018 to 2024
$2.8M
Chromosome 1q ceRNAs in Melanoma Progression and MetastasisR01CA259046 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI KARRETH, FLORIAN · 2021 to 2025
$2.3M
An ESC-GEMM platform for rapid melanoma mouse modelingR03CA227349 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI KARRETH, FLORIAN · 2018 to 2019
$172k
NCI NIH HHS P30 CA076292NCI NIH HHS R01 CA259046NCI NIH HHS R03 CA227349NCI NIH HHS R37 CA230042
6 · The paper itself

Abstract

Circular RNAs (circRNAs) are a class of non-coding RNAs featuring a covalently closed ring structure formed through backsplicing. circRNAs are broadly expressed and contribute to biological processes through a variety of functions. Standard gain-of-function and loss-of-function approaches to study gene functions have significant limitations when studying circRNAs. Overexpression studies in particular suffer from the lack of efficient genetic tools. While mammalian expression plasmids enable transient circRNA overexpression in cultured cells, most cell biological studies require long-term ectopic expression. Here we report the development and characterization of genetic tools enabling stable circRNA overexpression

Indexed as

MicroRNAsRNA, CircularAnimalsMammalsMiceRNARNA SplicingRNA, ViralMicroRNAsRNARNA, CircularRNA, ViralCircular RNAESC-GEMMmelanomamouse modelpiggyBacsleeping beautytransposon

Identifiers

PMID35289721
PMCPMC8928841
OpenAlexW4221011787

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.