Evidence map›Paper›PMID 25393766›Full record

ArticleAngewandte Chemie (International ed. in English)2015

Biocompatible infinite-coordination-polymer nanoparticle-nucleic-acid conjugates for antisense gene regulation.

Colin M Calabrese, Timothy J Merkel, William E Briley, Pratik S Randeria, Suguna P Narayan, Jessica L Rouge, David A Walker, Alexander W Scott, Chad A Mirkin

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Trial
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  8. Review
  9. Tumor cell lysate-loaded immunostimulatory spherical nucleic acids as therapeutics for triple-negative breast cancer.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. Article
  11. Article
  12. FeJournal of the American Chemical Society · 2019
    Article
  13. Article
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  15. Molecular spherical nucleic acids.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. 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

9 authors.

Colin M Calabrese *Department of Chemistry Northwestern University, Evanston, IL (USA).
Timothy J MerkelInternational Institute for Nanotechnology Northwestern University, Evanston, IL (USA).
William E BrileyInterdepartmental Biological Sciences Northwestern University, Evanston, IL (USA).
Pratik S RanderiaDepartment of Biomedical Engineering Northwestern University, Evanston, IL (USA).
Suguna P NarayanDepartment of Biomedical Engineering Northwestern University, Evanston, IL (USA).
Jessica L RougeInternational Institute for Nanotechnology Northwestern University, Evanston, IL (USA).
David A WalkerInternational Institute for Nanotechnology Northwestern University, Evanston, IL (USA).
Alexander W ScottDepartment of Biomedical Engineering Northwestern University, Evanston, IL (USA).
Chad A Mirkin *Department of Chemistry Northwestern University, Evanston, IL (USA).

Funding

Theranostic Magnetic Nanostructures for the Molecular Imaging of CancerU54CA151880 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A. · 2010 to 2014
$11.5M
NCI NIH HHS 3U54CA151880NCI NIH HHS U54 CA151880
6 · The paper itself

Abstract

Herein, we report the synthesis of DNA-functionalized infinite-coordination-polymer (ICP) nanoparticles as biocompatible gene-regulation agents. ICP nanoparticles were synthesized from ferric nitrate and a ditopic 3-hydroxy-4-pyridinone (HOPO) ligand bearing a pendant azide. Addition of Fe(III) to a solution of the ligand produced nanoparticles, which were colloidally unstable in the presence of salts. Conjugation of DNA to the Fe(III)-HOPO ICP particles by copper-free click chemistry afforded colloidally stable nucleic-acid nanoconstructs. The DNA-ICP particles, when cross-linked through sequence-specific hybridization, exhibited narrow, highly cooperative melting transitions consistent with dense DNA surface loading. The ability of the DNA-ICP particles to enter cells and alter protein expression was also evaluated. Our results indicate that these novel particles carry nucleic acids into mammalian cells without the need for transfection agents and are capable of efficient gene knockdown.

Indexed as

Antisense Elements (Genetics)Biocompatible MaterialsGene Expression RegulationHeLa CellsHumansMicroscopy, Atomic ForceNanoparticlesNucleic AcidsPolymersSpectrophotometry, UltravioletAntisense Elements (Genetics)Biocompatible MaterialsNucleic AcidsPolymersantisense gene regulationcoordination polymersgene knockdownironnanoparticles

Identifiers

PMID25393766
PMCPMC4314394

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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.