Evidence map›Paper›PMID 28437065›Full record

ArticleACS chemical biology2017

A Macrocyclic Peptide Ligand Binds the Oncogenic MicroRNA-21 Precursor and Suppresses Dicer Processing.

Matthew D Shortridge, Matthew J Walker, Tom Pavelitz, Yu Chen, Wen Yang, Gabriele Varani

Abstract read
In one paragraph

Article in ACS chemical biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

46 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
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  8. Article
  9. Structure of pre-miR-31 reveals an active role in Dicer-TRBP complex processing.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Structure of pre-miR-31 reveals an active role in Dicer processing.bioRxiv : the preprint server for biology · 2023
    Article
  14. Article
  15. Article
  16. RNA-Binding Macrocyclic Peptides.Frontiers in molecular biosciences · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. Article
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

6 authors at 1 institution in 1 country.

Matthew D ShortridgeDepartment of Chemistry, University of Washington, Seattle , Box 351700, Seattle, Washington 98195, United States.ORCID 0000-0003-2825-6836
Matthew J WalkerDepartment of Chemistry, University of Washington, Seattle , Box 351700, Seattle, Washington 98195, United States.
Tom PavelitzDepartment of Chemistry, University of Washington, Seattle , Box 351700, Seattle, Washington 98195, United States.
Yu ChenDepartment of Chemistry, University of Washington, Seattle , Box 351700, Seattle, Washington 98195, United States.
Wen YangDepartment of Chemistry, University of Washington, Seattle , Box 351700, Seattle, Washington 98195, United States.
Gabriele VaraniDepartment of Chemistry, University of Washington, Seattle , Box 351700, Seattle, Washington 98195, United States.
University of Washington · US

Funding

Regulation of microRNA processingR01GM103834 · NIGMS · UNIVERSITY OF WASHINGTON · PI VARANI, GABRIELE · 2014 to 2017
$1.1M
NIGMS NIH HHS R01 GM103834
6 · The paper itself

Abstract

MicroRNAs (miRNAs) help orchestrate cellular growth and survival through post-transcriptional mechanisms. The dysregulation of miRNA biogenesis can lead to cellular growth defects and chemotherapeutic resistance and plays a direct role in the development of many chronic diseases. Among these RNAs, miR-21 is consistently overexpressed in most human cancers, leading to the down-regulation of key tumor-suppressing and pro-apoptotic factors, suggesting that inhibition of miR-21 biogenesis could reverse these negative effects. However, targeted inhibition of miR-21 using small molecules has had limited success. To overcome difficulties in targeting RNA secondary structure with small molecules, we developed a class of cyclic β-hairpin peptidomimetics which bind to RNA stem-loop structures, such as miRNA precursors, with potent affinity and specificity. We screened an existing cyclic peptide library and discovered a lead structure which binds to pre-miR21 with K

Indexed as

AnimalsAnticarcinogenic AgentsCell LineDEAD-box RNA HelicasesHumansLigandsMicroRNAsPeptide LibraryPeptides, CyclicPeptidomimeticsProtein BindingRibonuclease IIIRNA Processing, Post-TranscriptionalSubstrate SpecificityAnticarcinogenic AgentsDEAD-box RNA HelicasesDICER1 protein, humanLigandsMicroRNAsMIRN21 microRNA, humanPeptide LibraryPeptides, CyclicPeptidomimeticsRibonuclease III

Identifiers

PMID28437065
PMCPMC5512579
OpenAlexW2608938455

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.