Evidence map›Paper›PMID 26985893›Full record

ArticleInternational journal of molecular sciences2016

A RNA-DNA Hybrid Aptamer for Nanoparticle-Based Prostate Tumor Targeted Drug Delivery.

John C Leach, Andrew Wang, Kaiming Ye, Sha Jin

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Biotechnology reports (Amsterdam, Netherlands) · 2024
    Review
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  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
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  13. Aptamers, the Nucleic Acid Antibodies, in Cancer Therapy.International journal of molecular sciences · 2020
    Review
  14. Article
  15. Review
  16. Review
  17. DNA Nanotechnology for Cancer Diagnosis and Therapy.International journal of molecular sciences · 2018
    Review
  18. Review
  19. Article
  20. Advances in the development of aptamer drug conjugates for targeted drug delivery.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    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 at 2 institutions in 1 country.

John C LeachDepartment of Biomedical Engineering, College of Engineering, University of Arkansas, Fayetteville, AR 72701, USA. jcleach@uams.edu.
Andrew WangOcean Nanotech, 2143 Worth Lane, Springdale, AR 72764, USA. awang@oceannanotech.com.
Kaiming YeDepartment of Biomedical Engineering, College of Engineering, University of Arkansas, Fayetteville, AR 72701, USA. kye@binghamton.edu.
Sha JinDepartment of Biomedical Engineering, College of Engineering, University of Arkansas, Fayetteville, AR 72701, USA. sjin@binghamton.edu.
University of Arkansas at Fayetteville · USOcean NanoTech (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The side effects of radio- and chemo-therapy pose long-term challenges on a cancer patient's health. It is, therefore, highly desirable to develop more effective therapies that can specifically target carcinoma cells without damaging normal and healthy cells. Tremendous efforts have been made in the past to develop targeted drug delivery systems for solid cancer treatment. In this study, a new aptamer, A10-3-J1, which recognizes the extracellular domain of the prostate specific membrane antigen (PSMA), was designed. A super paramagnetic iron oxide nanoparticle-aptamer-doxorubicin (SPIO-Apt-Dox) was fabricated and employed as a targeted drug delivery platform for cancer therapy. This DNA RNA hybridized aptamer antitumor agent was able to enhance the cytotoxicity of targeted cells while minimizing collateral damage to non-targeted cells. This SPIO-Apt-Dox nanoparticle has specificity to PSMA⁺ prostate cancer cells. Aptamer inhibited nonspecific uptake of membrane-permeable doxorubic to the non-target cells, leading to reduced untargeted cytotoxicity and endocytic uptake while enhancing targeted cytotoxicity and endocytic uptake. The experimental results indicate that the drug delivery platform can yield statistically significant effectiveness being more cytotoxic to the targeted cells as opposed to the non-targeted cells.

Indexed as

Antigens, SurfaceAntineoplastic AgentsAptamers, NucleotideCell Line, TumorCell ProliferationCell SurvivalDNADoxorubicinDrug Delivery SystemsGlutamate Carboxypeptidase IIHumansMagnetite NanoparticlesMaleProstatic NeoplasmsRNAAntigens, SurfaceAntineoplastic AgentsAptamers, NucleotideDNADoxorubicinFOLH1 protein, humanGlutamate Carboxypeptidase IIMagnetite NanoparticlesRNAaptamernanoparticleprostate cancertargeted drug delivery

Identifiers

PMID26985893
PMCPMC4813238
OpenAlexW2302415057

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.