Evidence map›Paper›PMID 29891903›Full record

ArticleNature communications2018

Modular cell-internalizing aptamer nanostructure enables targeted delivery of large functional RNAs in cancer cell lines.

David Porciani, Leah N Cardwell, Kwaku D Tawiah, Khalid K Alam, Margaret J Lange, Mark A Daniels, Donald H Burke

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Article
  3. MultiplexedNucleic acid therapeutics · 2024
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
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  11. Article
  12. Review
  13. Review
  14. Cancer immunomodulation using bispecific aptamers.Molecular therapy. Nucleic acids · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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 2 institutions in 1 country.

David PorcianiDepartment of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA. porcianid@missouri.edu.ORCID http://orcid.org/0000-0001-7803-6546
Leah N CardwellDepartment of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA.
Kwaku D TawiahBond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Khalid K AlamBond Life Sciences Center, University of Missouri, Columbia, MO, 65211, USA.
Margaret J LangeDepartment of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA.
Mark A DanielsDepartment of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA.
Donald H BurkeDepartment of Molecular Microbiology & Immunology, University of Missouri, Columbia, MO, 65212, USA. burkedh@missouri.edu.ORCID http://orcid.org/0000-0001-6513-8391
University of Missouri · USNorthwestern University · US

Funding

Gene Therapy for HIV Using Aptamers that Target Reverse TranscriptaseR01AI074389 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI BURKE, DONALD H · 2008 to 2017
$4.5M
Strain-specific and pan-filoviral aptamer recognition of Ebola virus glycoproteinsR21AI121938 · NIAID · UNIVERSITY OF MISSOURI-COLUMBIA · PI BURKE, DONALD H · 2016 to 2017
$427k
NIAID NIH HHS R01 AI074389NIAID NIH HHS R21 AI121938U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AI074389
6 · The paper itself

Abstract

Large RNAs and ribonucleoprotein complexes have powerful therapeutic potential, but effective cell-targeted delivery tools are limited. Aptamers that internalize into target cells can deliver siRNAs (<15 kDa, 19-21 nt/strand). We demonstrate a modular nanostructure for cellular delivery of large, functional RNA payloads (50-80 kDa, 175-250 nt) by aptamers that recognize multiple human B cell cancer lines and transferrin receptor-expressing cells. Fluorogenic RNA reporter payloads enable accelerated testing of platform designs and rapid evaluation of assembly and internalization. Modularity is demonstrated by swapping in different targeting and payload aptamers. Both modules internalize into leukemic B cell lines and remained colocalized within endosomes. Fluorescence from internalized RNA persists for ≥2 h, suggesting a sizable window for aptamer payloads to exert influence upon targeted cells. This demonstration of aptamer-mediated, cell-internalizing delivery of large RNAs with retention of functional structure raises the possibility of manipulating endosomes and cells by delivering large aptamers and regulatory RNAs.

Indexed as

AnimalsAptamers, NucleotideCell Line, TumorDogsDrug Delivery SystemsEndocytosisEndosomesFluorescent DyesHumansLeukemia, B-CellMicroscopy, ConfocalNanostructuresNanotechnologyNucleic Acid ConformationAptamers, NucleotideFluorescent Dyes

Identifiers

PMID29891903
PMCPMC5995956
OpenAlexW2805807586

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.