Evidence map›Paper›PMID 31546749›Full record

ArticleInternational journal of molecular sciences2019

Efficient Epidermal Growth Factor Receptor Targeting Oligonucleotide as a Potential Molecule for Targeted Cancer Therapy.

Tao Wang, Svetlana Philippovich, Jun Mao, Rakesh N Veedu

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  4. Article
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  7. Exosomes and exosome composite scaffolds in periodontal tissue engineering.Frontiers in bioengineering and biotechnology · 2023
    Review
  8. Composites of Nucleic Acids and Boron Clusters (CInternational journal of molecular sciences · 2021
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Aptamers in Non-Small Cell Lung Cancer Treatment.Molecules (Basel, Switzerland) · 2020
    Review
  15. Article
  16. Article
  17. 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 2 countries.

Tao WangCentre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth 6150, Australia. Tao.Wang@murdoch.edu.au.
Svetlana PhilippovichCentre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth 6150, Australia. 32351588@student.murdoch.edu.au.
Jun MaoCollege of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China. maojun1116@163.com.
Rakesh N VeeduCentre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth 6150, Australia. R.Veedu@murdoch.edu.au.ORCID 0000-0003-2192-9532
Murdoch University · AUDalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) is associated with the progression of a wide range of cancers including breast, glioma, lung, and liver cancer. The observation that EGFR inhibition can limit the growth of EGFR positive cancers has led to the development of various EGFR inhibitors including monoclonal antibodies and small-molecule inhibitors. However, the reported toxicity and drug resistance greatly compromised the clinical outcome of such inhibitors. As a type of chemical antibodies, nucleic acid aptamer provides an opportunity to overcome the obstacles faced by current EGFR inhibitors. In this study, we have developed and investigated the therapeutic potential of a 27mer aptamer CL-4RNV616 containing 2'-O-Methyl RNA and DNA nucleotides. Our results showed that CL-4RNV616 not only displayed enhanced stability in human serum, but also effectively recognized and inhibited the proliferation of EGFR positive Huh-7 liver cancer, MDA-MB-231 breast cancer, and U87MG glioblastoma cells, with an IC50 value of 258.9 nM, 413.7 nM, and 567.9 nM, respectively. Furthermore, TUNEL apoptosis assay revealed that CL-4RNV616 efficiently induced apoptosis of cancer cells. In addition, clinical breast cancer biopsy-based immunostaining assay demonstrated that CL-4RNV616 had a comparable detection efficacy for EGFR positive breast cancer with commonly used commercial antibodies. Based on the results, we firmly believe that CL-4RNV616 could be useful in the development of targeted cancer therapeutics and diagnostics.

Indexed as

Antineoplastic AgentsAptamers, NucleotideCell Line, TumorCell SurvivalDose-Response Relationship, DrugErbB ReceptorsHumansOligonucleotidesProtein StabilityRecombinant ProteinsAntineoplastic AgentsAptamers, NucleotideEGFR protein, humanErbB ReceptorsOligonucleotidesRecombinant ProteinsaptamersChemically-modified oligonucleotidesnucleic acids

Identifiers

PMID31546749
PMCPMC6801465
OpenAlexW2974184090

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.