Evidence map›Paper›PMID 32036231›Full record

ReviewCurrent opinion in chemical biology2020

Progress toward the development of the small molecule equivalent of small interfering RNA.

Matthew D Disney, Blessy M Suresh, Raphael I Benhamou, Jessica L Childs-Disney

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in chemical biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. [Targeting chimera technology: A new tool for undruggable in breast cancer].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Review
  2. The miRNomics of antiretroviral therapy-induced obesity.Functional & integrative genomics · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. DNA-encoded library versus RNA-encoded library selection enables design of an oncogenic noncoding RNA inhibitor.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Therapeutics in the Pipeline TargetingPharmacological reviews · 2022
    Review
  9. Article
  10. Review
  11. Review
  12. Drugging the "undruggable" microRNAs.Cellular and molecular life sciences : CMLS · 2021
    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 1 institution in 1 country.

Matthew D DisneyScripps Research, Department of Chemistry, 110 Scripps Way, Jupiter, FL, 33458, USA. Electronic address: disney@scripps.edu.
Blessy M SureshScripps Research, Department of Chemistry, 110 Scripps Way, Jupiter, FL, 33458, USA.
Raphael I BenhamouScripps Research, Department of Chemistry, 110 Scripps Way, Jupiter, FL, 33458, USA.
Jessica L Childs-DisneyScripps Research, Department of Chemistry, 110 Scripps Way, Jupiter, FL, 33458, USA.
Scripps Research Institute · US

Funding

Validation of r(G4C2)exp-binding small molecules in vivo and c9FTD/ALS biomarker developmentP01NS099114 · NINDS · UNIVERSITY OF FLORIDA · PI DISNEY, MATTHEW D, PETRUCELLI, LEONARD · 2017 to 2021
$6.5M
Using a disease-affected cell to synthesize its own drugDP1NS096898 · NINDS · SCRIPPS FLORIDA · PI DISNEY, MATTHEW D · 2015 to 2019
$5.0M
Sequence-based Design of Small Molecules Targeting RNAR01GM097455 · NIGMS · SCRIPPS FLORIDA · PI DISNEY, MATTHEW D · 2012 to 2019
$4.6M
Developing Novel RNA-Based Therapeutics for Parkinson's DiseaseR33NS096032 · NINDS · RBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL · PI DISNEY, MATTHEW D, MOURADIAN, M. MARAL · 2018 to 2019
$843k
NIGMS NIH HHS R01 GM097455NINDS NIH HHS DP1 NS096898NINDS NIH HHS P01 NS099114NINDS NIH HHS R33 NS096032
6 · The paper itself

Abstract

Given that many small molecules could bind to structured regions at sites that will not affect function, approaches that trigger degradation of RNA could provide a general way to affect biology. Indeed, targeted RNA degradation is an effective strategy to selectively and potently modulate biology. We describe several approaches to endow small molecules with the power to cleave RNAs. Central to these strategies is Inforna, which designs small molecules targeting RNA from human genome sequence. Inforna deduces the uniqueness of a druggable pocket, enables generation of hypotheses about functionality of the pocket, and defines on- and off-targets to drive compound optimization. RNA-binding compounds are then converted into cleavers that degrade the target directly or recruit an endogenous nuclease to do so. Cleaving compounds have significantly contributed to understanding and manipulating biological functions. Yet, there is much to be learned about how to affect human RNA biology with small molecules.

Indexed as

Base SequenceBleomycinDrug DesignDrug Evaluation, PreclinicalGenomeHumansMolecular Targeted TherapyMutationNucleic Acid ConformationRNA, Small InterferingRNA StabilitySmall Molecule LibrariesStructure-Activity RelationshipbleomycetinBleomycinRNA, Small InterferingSmall Molecule LibrariesAntisense oligonucleotidesNon-coding RNANucleic acidsRibonuclease targeting chimeras (RIBOTACs)RNAsiRNATargeted degradation

Identifiers

PMID32036231
PMCPMC7311281
OpenAlexW3004655307

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.