Evidence map›Paper›PMID 29545334›Full record

ArticleMolecular cancer therapeutics2018

ICEC0942, an Orally Bioavailable Selective Inhibitor of CDK7 for Cancer Treatment.

Hetal Patel, Manikandan Periyasamy, Georgina P Sava, Alexander Bondke, Brian W Slafer, Sebastian H B Kroll, Marion Barbazanges, Richard Starkey, Silvia Ottaviani, Alison Harrod and 6 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

79 citing papers in PubMed, 138 citations in OpenAlex.

  1. Article
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  3. Targeting CDKs in the RNAPII transcription cycle.Nature reviews. Drug discovery · 2026
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19 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

16 authors at 2 institutions in 1 country.

Hetal PatelDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
Manikandan PeriyasamyDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
Georgina P SavaDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
Alexander BondkeDepartment of Chemistry, Imperial College London, London, United Kingdom.
Brian W SlaferDepartment of Chemistry, Imperial College London, London, United Kingdom.
Sebastian H B KrollDepartment of Chemistry, Imperial College London, London, United Kingdom.
Marion BarbazangesDepartment of Chemistry, Imperial College London, London, United Kingdom.
Richard StarkeyDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
Silvia OttavianiDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.ORCID 0000-0002-8830-9947
Alison HarrodDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
Eric O AboagyeComprehensive Cancer Imaging Centre, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
Laki BuluwelaDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
Matthew J FuchterDepartment of Chemistry, Imperial College London, London, United Kingdom.
Anthony G M BarrettDepartment of Chemistry, Imperial College London, London, United Kingdom.
R Charles CoombesDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom. simak.ali@imperial.ac.uk c.coombes@imperial.ac.uk.
Simak AliDivision of Cancer, Department of Surgery & Cancer, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom. simak.ali@imperial.ac.uk c.coombes@imperial.ac.uk.
Hammersmith Hospital · GBImperial College London · GB

Funding

Cancer Research UK 12011Cancer Research UK 18784Cancer Research UK C37/A12011Cancer Research UK C37/A18784Cancer Research UK C37/A9335Department of Health
6 · The paper itself

Abstract

Recent reports indicate that some cancer types are especially sensitive to transcription inhibition, suggesting that targeting the transcriptional machinery provides new approaches to cancer treatment. Cyclin-dependent kinase (CDK)7 is necessary for transcription, and acts by phosphorylating the C-terminal domain (CTD) of RNA polymerase II (PolII) to enable transcription initiation. CDK7 additionally regulates the activities of a number of transcription factors, including estrogen receptor (ER)-α. Here we describe a new, orally bioavailable CDK7 inhibitor, ICEC0942. It selectively inhibits CDK7, with an IC

Indexed as

Administration, OralAnimalsAntineoplastic AgentsBiological AvailabilityCaspasesCell CycleCell Line, TumorCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesDisease Models, AnimalDose-Response Relationship, DrugHumansMicePhosphorylationProtein Kinase InhibitorsXenograft Model Antitumor AssaysAntineoplastic AgentsCaspasesCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesProtein Kinase Inhibitors

Identifiers

PMID29545334
PMCPMC5985928
OpenAlexW2792645148

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.