Evidence map›Paper›PMID 23020598›Full record

ArticleJournal of the American Chemical Society2012

Antibody-linked spherical nucleic acids for cellular targeting.

Ke Zhang, Liangliang Hao, Sarah J Hurst, Chad A Mirkin

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
–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

59 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Formation and cellular uptake of Bleomycin saccharide decorated molecular spherical nucleic acids evaluated by time-resolved fluorescence spectroscopy.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. DNA Transformations for Diagnosis and Therapy.Advanced functional materials · 2021
    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

4 authors.

Ke ZhangDepartment of Chemistry and the International Institute for Nanotechnology, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, USA.
Liangliang Hao
Sarah J Hurst
Chad A Mirkin

Funding

Theranostic Magnetic Nanostructures for the Molecular Imaging of CancerU54CA151880 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WOLOSCHAK, GAYLE E. · 2010 to 2014
$11.5M
The Role of Keratinocytes as Independent ThermosensorsP30AR057216 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PEREZ WHITE, BETHANY E · 2009 to 2018
$6.0M
Topical Delivery of siRNA Nanconjugates: Suppressing Epidermal HyperplasiaR01AR060810 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A., PALLER, AMY S · 2012 to 2015
$1.3M
siRNA-gold nanoparticle mediated ganglioside depletion for diabetic wound healingR21AR062898 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A., PALLER, AMY S · 2012 to 2013
$455k
NCI NIH HHS U54 CA151880NIAMS NIH HHS P30 AR057216NIAMS NIH HHS R01 AR060810NIAMS NIH HHS R01AR060810NIAMS NIH HHS R21 AR062898NIAMS NIH HHS R21AR062898
6 · The paper itself

Abstract

Spherical nucleic acid (SNA) constructs are promising new single entity gene regulation materials capable of both cellular transfection and gene knockdown, but thus far are promiscuous structures, exhibiting excellent genetic but little cellular selectivity. In this communication, we describe a strategy to impart targeting capabilities to these constructs through noncovalent functionalization with a complementary antibody-DNA conjugate. As a proof-of-concept, we designed HER2-targeting SNAs and demonstrated that such structures exhibit cell type selectivity in terms of their uptake, and significantly greater gene knockdown in cells overexpressing the target antigen as compared to the analogous antibody-free and off-target materials.

Indexed as

Antibodies, MonoclonalCell Line, TumorDNA, AntisenseErb-b2 Receptor Tyrosine KinasesGene Knockdown TechniquesHumansImmunoconjugatesModels, MolecularAntibodies, MonoclonalDNA, AntisenseErb-b2 Receptor Tyrosine KinasesImmunoconjugates

Identifiers

PMID23020598
PMCPMC3501255

What OpenQuestion holds

Textmetadata
LicenceTDM
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.