Evidence map›Paper›PMID 22492537›Full record

ArticleChemistry, an Asian journal2012

Self-assembled aptamer-based drug carriers for bispecific cytotoxicity to cancer cells.

Guizhi Zhu, Ling Meng, Mao Ye, Liu Yang, Kwame Sefah, Meghan B O'Donoghue, Yan Chen, Xiangling Xiong, Jin Huang, Erqun Song and 1 more

Abstract read
In one paragraph

Article in Chemistry, an Asian journal, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Novel insights into the role of aptamers in the fight against cancer.Journal of cancer research and clinical oncology · 2019
    Review
  6. Review
  7. Article
  8. Review
  9. Advances in the development of aptamer drug conjugates for targeted drug delivery.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    Review
  10. Aptamer-Mediated Targeted Delivery of Therapeutics: An Update.Pharmaceuticals (Basel, Switzerland) · 2016
    Review
  11. Review
  12. Aptamer-Drug Conjugates.Bioconjugate chemistry · 2015
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Gold-Coated FeAdvanced functional materials · 2014
    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

11 authors.

Guizhi ZhuDepartment of Chemistry, Shands Cancer Center, UF Genetics Institute, University of Florida, Gainesville, Florida 32611-7200, USA.
Ling Meng
Mao Ye
Liu Yang
Kwame Sefah
Meghan B O'Donoghue
Yan Chen
Xiangling Xiong
Jin Huang
Erqun Song
Weihong Tan

Funding

Real-Time and Quantitative Determination of GenesR01GM066137 · NIGMS · UNIVERSITY OF FLORIDA · PI TAN, WEIHONG · 2002 to 2010
$2.2M
Molecular Target for Liver Cancer Diagnosis and TherapyR01CA133086 · NCI · UNIVERSITY OF FLORIDA · PI LIU, CHEN · 2009 to 2013
$1.5M
NCI NIH HHS CA133086NCI NIH HHS R01 CA133086NIGMS NIH HHS GM066137NIGMS NIH HHS R01 GM066137
6 · The paper itself

Abstract

Monovalent aptamers can deliver drugs to target cells by specific recognition. However, different cancer subtypes are distinguished by heterogeneous biomarkers and one single aptamer is unable to recognize all clinical samples from different patients with even the same type of cancers. To address heterogeneity among cancer subtypes for targeted drug delivery, as a model, we developed a drug carrier with a broader recognition range of cancer subtypes. This carrier, sgc8c-sgd5a (SD), was self-assembled from two modified monovalent aptamers. It showed bispecific recognition abilities to target cells in cell mixtures; thus broadening the recognition capabilities of its parent aptamers. The self-assembly of SD simultaneously formed multiple drug loading sites for the anticancer drug doxorubicin (Dox). The Dox-loaded SD (SD-Dox) also showed bispecific abilities for target cell binding and drug delivery. Most importantly, SD-Dox induced bispecific cytotoxicity in target cells in cell mixtures. Therefore, by broadening the otherwise limited recognition capabilities of monovalent aptamers, bispecific aptamer-based drug carriers would facilitate aptamer applications for clinically heterogeneous cancer subtypes that respond to the same cancer therapy.

Indexed as

Drug Delivery SystemsAntibiotics, AntineoplasticAptamers, NucleotideCell Line, TumorCell Membrane PermeabilityCell SurvivalDoxorubicinHumansNeoplasmsAntibiotics, AntineoplasticAptamers, NucleotideDoxorubicin

Identifiers

PMID22492537
PMCPMC3475610

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Registered trials

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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.