Evidence map›Paper›PMID 23834155›Full record

ReviewCurrent drug targets2013

Nuclear export mediated regulation of microRNAs: potential target for drug intervention.

Irfana Muqbil, Bin Bao, Abdul Badi Abou-Samra, Ramzi M Mohammad, Asfar S Azmi

Open access · greenAbstract readReview
In one paragraph

Review in Current drug targets, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. MicroRNAs in diabetes mellitus.Journal of diabetes and metabolic disorders · 2025
    Review
  3. Review
  4. Review
  5. Treatment of multiple myeloma with selinexor: a review.Therapeutic advances in hematology · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Targeting Nuclear Exporter Protein XPO1/CRM1 in Gastric Cancer.International journal of molecular sciences · 2019
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Exportin-5 Functions as an Oncogene and a Potential Therapeutic Target in Colorectal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Article
  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

5 authors at 2 institutions in 2 countries.

Irfana MuqbilDepartment of Biochemistry Faculty of Life Sciences, AMU Aligarh, 202002 UP, India.
Bin Bao
Abdul Badi Abou-Samra
Ramzi M Mohammad
Asfar S Azmi
Hamad Medical Corporation · QAWayne State University · US

Funding

Differential Network Interrogations of Epithelial to Mesenchymal TransitionR21CA175974 · NCI · WAYNE STATE UNIVERSITY · PI MOHAMMAD, RAMZI M., REDDY, CHANDAN · 2013 to 2014
$359k
Development of Small Molecule Crm-1 Inhibitor for Pancreatic Cancer TherapyR21CA169848 · NCI · WAYNE STATE UNIVERSITY · PI MOHAMMAD, RAMZI M. · 2012 to 2013
$354k
NCI NIH HHS 1R21CA17597401NCI NIH HHS R21 1R21CA16984801NCI NIH HHS R21 CA169848NCI NIH HHS R21 CA175974
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are short non-coding RNAs that have been recognized to regulate the expression of uncountable number of genes. Their aberrant expression has been found to be linked to the pathology of many diseases including cancer. There is a drive to develop miRNA targeted therapeutics for different diseases especially cancer. Nevertheless, reining in these short non-coding RNAs is not as straightforward as originally thought. This is in view of the recent discoveries that miRNAs are under epigenetic regulations at multiple levels. Exportin 5 protein (XPO5) nuclear export mediated regulation of miRNAs is one such important epigenetic mechanism. XPO5 is responsible for exporting precursor miRNAs through the nuclear membrane to the cytoplasm, and is thus a critical step in miRNA biogenesis. A number of studies have shown that variations in components of the miRNA biogenesis pathways, particularly the aberrant expression of XPO5, increase the risk of developing cancer. In addition to XPO5, the Exportin 1 protein (XPO1) or chromosome region maintenance 1 (CRM1) can also carry miRNA export function. These findings are supported by pathway analyses that reveal certain miRNAs as direct interaction partners of CRM1. An in depth understanding of miRNA export mediated regulatory mechanisms is important for the successful design of clinically viable therapeutics. In this review, we describe the current knowledge on the mechanisms of miRNA nuclear transport mediated regulation and propose strategies to selectively block this important mechanism in cancer.

Indexed as

Active Transport, Cell NucleusAnimalsAntineoplastic AgentsCell NucleusCytoplasmEpigenesis, GeneticExportin 1 ProteinGene Expression Regulation, NeoplasticHumansKaryopherinsMicroRNAsMolecular Targeted TherapyNeoplasmsReceptors, Cytoplasmic and NuclearRNA-Binding ProteinsAntineoplastic AgentsExportin 1 ProteinKaryopherinsMicroRNAsReceptors, Cytoplasmic and NuclearRNA-Binding ProteinsXPO5 protein, human

Identifiers

PMID23834155
PMCPMC4167361
OpenAlexW2061492517

What OpenQuestion holds

Textmetadata
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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.