Evidence map›Paper›PMID 25377905›Full record

ArticleChemistry, an Asian journal2015

Aptamer CaCO3 nanostructures: a facile, pH-responsive, specific platform for targeted anticancer theranostics.

Cuisong Zhou, Tao Chen, Cuichen Wu, Guizhi Zhu, Liping Qiu, Cheng Cui, Weijia Hou, Weihong Tan

Open access · greenAbstract read
In one paragraph

Article in Chemistry, an Asian journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. pH-dependent and cathepsin B activable CaCOInternational journal of nanomedicine · 2019
    Article
  7. Aptamer-based targeted therapy.Advanced drug delivery reviews · 2018
    Review
  8. Review
  9. Article
  10. Article
  11. Core-shell NaGdFScientific reports · 2017
    Article
  12. Advances in the development of aptamer drug conjugates for targeted drug delivery.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    Review
  13. Article
  14. Article
  15. Review
  16. Aptamer-Drug Conjugates.Bioconjugate chemistry · 2015
    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

8 authors at 4 institutions in 2 countries.

Cuisong ZhouCollege of Chemistry, Sichuan University, Chengdu, 610064 (P.R. China); Department of Chemistry and Physiology and Functional Genomics, Center for Research at the Bio/Nano Interface, Shands Cancer Center, University of Florida, Gainesville, FL 32611-7200 (USA), Fax: (+1) 352-846-2410.
Tao Chen
Cuichen Wu
Guizhi Zhu
Liping Qiu
Cheng Cui
Weijia Hou
Weihong Tan
University of Florida · USHunan University · CNInterface (United States) · USUniversity of Florida Health · US

Funding

Development of molecular probes for biomedical applicationsR01GM079359 · NIGMS · UNIVERSITY OF FLORIDA · PI TAN, WEIHONG · 2007 to 2016
$2.3M
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 GM079359NIGMS NIH HHS R01 GM079359
6 · The paper itself

Abstract

The application of cancer theranostics depends on the development of multifunctional nanostructured platforms for accurate cell targeting and controlled drug release, imaging, and therapy. Herein, a comprehensive, easily fabricated anticancer theranostic platform with a high drug-loading capacity, termed an aptamer-functionalized calcium carbonate (CaCO3 ) nanostructure (apt-CCN), is reported. Flow cytometry and confocal fluorescence microscopy studies demonstrate that apt-CCNs can specifically bind to target cancer cells, but not to control cells, and that they possess highly efficient internalization to target cancer cells. This smart nanostructure selectively reaches the lysosomes through receptor-mediated endocytosis and is responsive to the relatively low lysosome pH (4.5-5.5), which facilitates the release of doxorubicin. The apt-CCN platform offers targeted and efficient drug transport, as well as target-specific delivery of imaging agents for cancer diagnosis and therapy.

Indexed as

Antineoplastic AgentsAptamers, NucleotideCalcium CarbonateCell Line, TumorCell SurvivalDoxorubicinDrug CarriersHumansHydrogen-Ion ConcentrationLysosomesMicroscopy, ConfocalNanostructuresAntineoplastic AgentsAptamers, NucleotideCalcium CarbonateDoxorubicinDrug Carriersaptamerscancerdrug deliverynanostructurestheranostics

Identifiers

PMID25377905
PMCPMC4323099
OpenAlexW2055509681

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.