Evidence map›Paper›PMID 25835969›Full record

ReviewTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

Transcription factor decoy: a pre-transcriptional approach for gene downregulation purpose in cancer.

Seyed Mohammad Ali Hosseini Rad, Lida Langroudi, Fatemeh Kouhkan, Laleh Yazdani, Alireza Nouri Koupaee, Sara Asgharpour, Zahra Shojaei, Taravat Bamdad, Ehsan Arefian

Abstract readReview
PubMed Publisher
In one paragraph

Review in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Expanding Catch and Release DNA Decoy (CRDD) Technology with Pyrimidine Mimics.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022
    Article
  5. Review
  6. Decoy Technology as a Promising Therapeutic Tool for Atherosclerosis.International journal of molecular sciences · 2021
    Review
  7. Article
  8. Nuclear Receptors, Ligands and the Mammalian B Cell.International journal of molecular sciences · 2020
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. MicroRNAs modulating angiogenesis: miR-129-1 and miR-133 act as angio-miR in HUVECs.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  17. Article
  18. NF-κB as a Therapeutic Target in Inflammatory-Associated Bone Diseases.Advances in protein chemistry and structural biology
    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

9 authors.

Seyed Mohammad Ali Hosseini RadDepartment of Molecular Biology and Genetic Engineering, Stem Cell Technology Research Center, 1997775555, Tehran, Iran, a.hoseini.rad@gmail.com.
Lida Langroudi
Fatemeh Kouhkan
Laleh Yazdani
Alireza Nouri Koupaee
Sara Asgharpour
Zahra Shojaei
Taravat Bamdad
Ehsan Arefian

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene therapy as a therapeutic approach has been the dream for many scientists around the globe. Many strategies have been proposed and applied for this purpose, yet the void for a functional safe method is still apparent. Since most of the diseases are caused by undesirable upregulation (oncogenes) or downregulation (tumor suppressor genes) of genes, major gene therapy's techniques affect gene expression. Most of the methods are used in post-transcriptional level such as RNA inhibitory (RNAi) and splice-switching oligonucleotides (SSOs). RNAi blocks messenger RNA (mRNA) translation by mRNA degradation or interruption between attachments of mRNA with ribosomes' subunits. However, one of the novel methods is the usage of transcription factor targeted decoys. DNA decoys are the new generation of functional gene downregulatory oligonucleotides which compete with specific binding sites of transcription factors. Considering the exponential growth of this technique in both in vitro and in vivo studies, in this paper, we aim to line out the description, design, and application of decoys in research and therapy.

Indexed as

Genetic TherapyTranscription, GeneticBinding SitesGene Expression Regulation, NeoplasticHumansNeoplasmsNF-kappa BOligodeoxyribonucleotidesRNA InterferenceRNA, MessengerTranscription FactorsNF-kappa BOligodeoxyribonucleotidesRNA, MessengerTranscription Factors

Identifiers

What OpenQuestion holds

Textmetadata
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.