Evidence map›Paper›PMID 34834316›Full record

ReviewPharmaceutics2021

miRNA Delivery by Nanosystems: State of the Art and Perspectives.

Fernanda C Moraes, Chantal Pichon, Didier Letourneur, Frédéric Chaubet

Abstract readReview
In one paragraph

Review in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–field-weighted citation impact
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

42 citing papers in PubMed.

  1. Review
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  14. MiRNA-based drugs: challenges and delivery strategies.Applied microbiology and biotechnology · 2025
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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

4 authors.

Fernanda C MoraesLVTS, INSERM U1148, Université Sorbonne Paris Nord, Université de Paris, 75018 Paris, France.
Chantal PichonCentre de Biophysique Moléculaire, CNRS UPR4301, Université d'Orléans, 45071 Orléans, France.ORCID 0000-0003-3161-3937
Didier LetourneurLVTS, INSERM U1148, Université Sorbonne Paris Nord, Université de Paris, 75018 Paris, France.ORCID 0000-0003-2197-9468
Frédéric ChaubetLVTS, INSERM U1148, Université Sorbonne Paris Nord, Université de Paris, 75018 Paris, France.ORCID 0000-0001-7375-0425

Funding

National Council for Scientific and Technological Development 201245/2017-5
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are short (~21-23 nucleotides), non-coding endogenous RNA molecules that modulate gene expression at the post-transcriptional level via the endogenous RNA interference machinery of the cell. They have emerged as potential biopharmaceuticals candidates for the treatment of various diseases, including cancer, cardiovascular and metabolic diseases. However, in order to advance miRNAs therapeutics into clinical settings, their delivery remains a major challenge. Different types of vectors have been investigated to allow the delivery of miRNA in the diseased tissue. In particular, non-viral delivery systems have shown important advantages such as versatility, low cost, easy fabrication and low immunogenicity. Here, we present a general overview of the main types of non-viral vectors developed for miRNA delivery, with their advantages, limitations and future perspectives.

Indexed as

miRNA deliverynanoparticlesnon-viral vectors

Identifiers

PMID34834316
PMCPMC8619868

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.