Evidence map›Paper›PMID 31664817›Full record

ReviewACS nano2019

Aptamers as Modular Components of Therapeutic Nucleic Acid Nanotechnology.

Martin Panigaj, M Brittany Johnson, Weina Ke, Jessica McMillan, Ekaterina A Goncharova, Morgan Chandler, Kirill A Afonin

Abstract readReview
In one paragraph

Review in ACS nano, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

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  19. Mechanisms, Techniques and Devices of Airborne Virus Detection: A Review.International journal of environmental research and public health · 2023
    Review
  20. Article

1 more citing papers are in PubMed but not listed here.

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.

Martin PanigajNanoscale Science Program, Department of Chemistry , University of North Carolina at Charlotte , Charlotte , North Carolina 28223 , United States.
M Brittany JohnsonDepartment of Biological Sciences , University of North Carolina at Charlotte , Charlotte , North Carolina 28223 , United States.
Weina KeNanoscale Science Program, Department of Chemistry , University of North Carolina at Charlotte , Charlotte , North Carolina 28223 , United States.
Jessica McMillanNanoscale Science Program, Department of Chemistry , University of North Carolina at Charlotte , Charlotte , North Carolina 28223 , United States.
Ekaterina A GoncharovaNanoscale Science Program, Department of Chemistry , University of North Carolina at Charlotte , Charlotte , North Carolina 28223 , United States.
Morgan ChandlerNanoscale Science Program, Department of Chemistry , University of North Carolina at Charlotte , Charlotte , North Carolina 28223 , United States.
Kirill A AfoninNanoscale Science Program, Department of Chemistry , University of North Carolina at Charlotte , Charlotte , North Carolina 28223 , United States.ORCID 0000-0002-6917-3183

Funding

Characterization of various multifunctional nucleic acid nanoparticles and understanding their immunotoxicityR01GM120487 · NIGMS · UNIVERSITY OF NORTH CAROLINA CHARLOTTE · PI AFONIN, KIRILL A · 2017 to 2020
$1.5M
NIGMS NIH HHS R01 GM120487
6 · The paper itself

Abstract

Nucleic acids play a central role in all domains of life, either as genetic blueprints or as regulators of various biochemical pathways. The chemical makeup of ribonucleic acid (RNA) or deoxyribonucleic acid (DNA), generally represented by a sequence of four monomers, also provides precise instructions for folding and higher-order assembly of these biopolymers that, in turn, dictate biological functions. The sequence-based specific 3D structures of nucleic acids led to the development of the directed evolution of oligonucleotides, SELEX (systematic evolution of ligands by exponential enrichment), against a chosen target molecule. Among the variety of functions, selected oligonucleotides named aptamers also allow targeting of cell-specific receptors with antibody-like precision and can deliver functional RNAs without a transfection agent. The advancements in the field of customizable nucleic acid nanoparticles (NANPs) opened avenues for the design of nanoassemblies utilizing aptamers for triggering or blocking cell signaling pathways or using aptamer-receptor combinations to activate therapeutic functionalities. A recent selection of fluorescent aptamers enables real-time tracking of NANP formation and interactions. The aptamers are anticipated to contribute to the future development of technologies, enabling an efficient assembly of functional NANPs in mammalian cells or

Indexed as

Aptamers, NucleotideNanoparticlesAnimalsCell Line, TumorDrug Delivery SystemsHumansImmunotherapyMiceNanomedicineNeoplasmsNucleic AcidsSELEX Aptamer TechniqueAptamers, NucleotideNucleic AcidsaptamersexosomesimmunotherapyNANPsnucleic acid deliveryRNA nanotechnologySELEXtherapeutic nucleic acids

Identifiers

PMID31664817
PMCPMC7382785

What OpenQuestion holds

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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.