Evidence map›Paper›PMID 22885522›Full record

ReviewDrug discovery today2013

The development and application of small molecule modulators of SF3b as therapeutic agents for cancer.

Thomas R Webb, Amanda S Joyner, Philip M Potter

Open access · greenAbstract readReview
In one paragraph

Review in Drug discovery today, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

66 citing papers in PubMed, 99 citations in OpenAlex.

  1. Review
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  5. Life science alliance · 2023
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  20. Targeting mRNA processing as an anticancer strategy.Nature reviews. Drug discovery · 2020
    Review

6 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Thomas R WebbDepartment of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA.
Amanda S Joyner
Philip M Potter
St. Jude Children's Research Hospital · US

Funding

Synthetic Spliceosome Probes and ModulatorsR01CA140474 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI WEBB, THOMAS ROY · 2010 to 2014
$1.7M
NCI NIH HHS R01 CA140474
6 · The paper itself

Abstract

The identification of potent spliceosome modulators that demonstrate antitumor activity indicates that this complex may be a target for drug development. Several natural products have been demonstrated to bind to the SF3b1 subunit of this macromolecule and these agents modulate alternative RNA splicing. In this article we describe their biological properties, discuss the validity of the spliceosome as a therapeutic target, and propose that alteration of alternative splicing represents a viable approach for inducing tumor-selective cytotoxicity.

Indexed as

Drug DesignAlternative SplicingAnimalsAntineoplastic AgentsHumansMolecular Targeted TherapyNeoplasmsPhosphoproteinsRibonucleoprotein, U2 Small NuclearRNA Splicing FactorsSpliceosomesAntineoplastic AgentsPhosphoproteinsRibonucleoprotein, U2 Small NuclearRNA Splicing FactorsSF3B1 protein, human

Identifiers

PMID22885522
PMCPMC3596818
OpenAlexW2139948978

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.