Evidence map›Paper›PMID 19823169›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2009

Using an RNA aptamer probe for flow cytometry detection of CD30-expressing lymphoma cells.

Peng Zhang, Nianxi Zhao, Zihua Zeng, Yongdong Feng, Ching-Hsuan Tung, Chung-Che Chang, Youli Zu

Open access · hybridAbstract readValidation Study
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

33 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Aptamer-based approaches forResearch in pharmaceutical sciences · 2020
    Review
  9. Article
  10. Silencing RORγt in Human CD4Scientific reports · 2019
    Article
  11. Article
  12. Article
  13. Aptamers as Diagnostic Tools in Cancer.Pharmaceuticals (Basel, Switzerland) · 2018
    Review
  14. Aptamer-based targeted therapy.Advanced drug delivery reviews · 2018
    Review
  15. Affinity capture of aflatoxin BMikrochimica acta · 2018
    Article
  16. Review
  17. Review
  18. Aptamer-Drug Conjugates.Bioconjugate chemistry · 2015
    Review
  19. Review
  20. 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

7 authors at 2 institutions in 2 countries.

Peng ZhangDepartment of Pathology, The Methodist Hospital and The Methodist Hospital Research Institute, Houston, TX 77030, USA.
Nianxi Zhao
Zihua Zeng
Yongdong Feng
Ching-Hsuan Tung
Chung-Che Chang
Youli Zu
Houston Methodist · USMethodist Hospital · US

Funding

A bifunctional nanomedicine for both specific imaging and targeting therapy of anR01CA151955 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI ZU, YOULI · 2010 to 2014
$1.5M
Role of MAP kinases in anaplastic large cell lymphomaK22CA113493 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI ZU, YOULI · 2007 to 2009
$454k
NCI NIH HHS 5K22CA113493NCI NIH HHS K22 CA113493NCI NIH HHS R01 CA151955
6 · The paper itself

Abstract

Aptamers are small molecular ligands composed of short oligonucleotides that bind targets with high affinity. In contrast to antibodies, as synthetic oligonucleotides, aptamers have lower production costs and elicit no antigenic reactions. Therefore, aptamers are potential agents for disease diagnosis and treatment. In this study, we validate a fluorescently labeled RNA aptamer, which has been reported to bind specifically to mouse CD30 proteins in solution, for human CD30 protein recognition on intact cells. The aptamer probe was tested with cultured anaplastic large cell lymphoma and Hodgkin's lymphoma cells that express high levels of CD30. Flow cytometry and fluorescence microscopy showed specific and sensitive binding of the aptamer probe to CD30-expressing lymphoma cells at low concentrations (0.3 nM). Studies performed on multiple cell lines and nuclear cells from healthy donors confirmed that the CD30 aptamer and anti-CD30 antibody, the standard clinical probe, recognized the same set of cells. The potential application of multicolor flow cytometry analysis using the CD30 aptamer probe and antibodies was also shown. In conclusion, the developed CD30 aptamer probe could act as a replacement and/or a supplement for antibodies in the diagnosis of the CD30-expressing lymphomas.

Indexed as

Aptamers, NucleotideMolecular Probe TechniquesAnimalsAntibodiesCell Line, TumorFlow CytometryHumansImmunophenotypingKi-1 AntigenLymphomaMiceSensitivity and SpecificityAntibodiesAptamers, NucleotideKi-1 Antigen

Identifiers

PMID19823169
PMCPMC3763839
OpenAlexW2135493243

What OpenQuestion holds

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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.