Evidence map›Paper›PMID 29286300›Full record

ArticleMolecules (Basel, Switzerland)2017

A Peptide Nucleic Acid against MicroRNA miR-145-5p Enhances the Expression of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) in Calu-3 Cells.

Enrica Fabbri, Anna Tamanini, Tiziana Jakova, Jessica Gasparello, Alex Manicardi, Roberto Corradini, Giuseppe Sabbioni, Alessia Finotti, Monica Borgatti, Ilaria Lampronti and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 50 citations in OpenAlex.

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  18. Multifunctional Delivery Systems for Peptide Nucleic Acids.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  19. The Multifaceted Roles of MicroRNAs in Cystic Fibrosis.Diagnostics (Basel, Switzerland) · 2020
    Review
  20. 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

14 authors at 3 institutions in 1 country.

Enrica FabbriDepartment of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy. enrica.fabbri@unife.it.
Anna TamaniniLaboratory of Molecular Pathology, University-Hospital, 37126 Verona, Italy. anna.tamanini@aovr.veneto.it.
Tiziana JakovaDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, 43124 Parma, Italy. tiziana.jakova@studenti.unipr.it.
Jessica GasparelloDepartment of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy. gspjsc@unife.it.
Alex ManicardiDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, 43124 Parma, Italy. Alex.manicardi@ugent.be.ORCID 0000-0003-0083-1392
Roberto CorradiniDepartment of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, 43124 Parma, Italy. roberto.corradini@unipr.it.
Giuseppe SabbioniDepartment of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy. giuseppe.sabbioni@student.unife.it.
Alessia FinottiDepartment of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy. alessia.finotti@unife.it.ORCID 0000-0002-7638-515X
Monica BorgattiDepartment of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy. monica.borgatti@unife.it.
Ilaria LamprontiDepartment of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy. ilaria.lampronti@unife.it.
Silvia MunariLaboratory of Molecular Pathology, University-Hospital, 37126 Verona, Italy. silvia.munari88@gmail.com.
Maria Cristina DechecchiLaboratory of Molecular Pathology, University-Hospital, 37126 Verona, Italy. cristina.dechecchi@ospedaleuniverona.it.
Giulio CabriniLaboratory of Molecular Pathology, University-Hospital, 37126 Verona, Italy. giulio.cabrini@univr.it.
Roberto GambariDepartment of Life Sciences and Biotechnology, University of Ferrara, 44121 Ferrara, Italy. gam@unife.it.
University of Ferrara · ITUniversity of Verona · ITUniversity of Parma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peptide nucleic acids (PNAs) are very useful tools for gene regulation at different levels, but in particular in the last years their use for targeting microRNA (anti-miR PNAs) has provided impressive advancements. In this respect, microRNAs related to the repression of cystic fibrosis transmembrane conductance regulator (CFTR) gene, which is defective in cystic fibrosis, are of great importance in the development of new type of treatments. In this paper we propose the use of an anti-miR PNA for targeting miR-145, a microRNA reported to suppress CFTR expression. Octaarginine-anti-miR PNA conjugates were delivered to Calu-3 cells, exerting sequence dependent targeting of miR-145-5p. This allowed to enhance expression of the miR-145 regulated CFTR gene, analyzed at mRNA (RT-qPCR, Reverse Transcription quantitative Polymerase Chain Reaction) and CFTR protein (Western blotting) level.

Indexed as

3' Untranslated RegionsApoptosisBase SequenceBinding SitesCell LineCell ProliferationCystic Fibrosis Transmembrane Conductance RegulatorEvolution, MolecularGene Expression RegulationHumansMicroRNAsPeptide Nucleic AcidsRNA, MessengerUp-Regulation3' Untranslated RegionsCystic Fibrosis Transmembrane Conductance RegulatorMicroRNAsMIRN145 microRNA, humanPeptide Nucleic AcidsRNA, MessengerCFTRcystic fibrosisdeliverymicroRNAsmiR-145miRNA targetingpeptide nucleic acids

Identifiers

PMID29286300
PMCPMC6017273
OpenAlexW2775867554

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.