Evidence map›Paper›PMID 31248103›Full record

ReviewPharmaceuticals (Basel, Switzerland)2019

CDK8-Novel Therapeutic Opportunities.

Ingeborg Menzl, Agnieszka Witalisz-Siepracka, Veronika Sexl

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 50 citations in OpenAlex.

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  20. Gene Transcription as a Therapeutic Target in Leukemia.International journal of molecular sciences · 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

3 authors at 1 institution in 1 country.

Ingeborg MenzlInstitute of Pharmacology and Toxicology, University of Veterinary Medicine, 1210 Vienna, Austria. Ingeborg.menzl@vetmeduni.ac.at.
Agnieszka Witalisz-SieprackaInstitute of Pharmacology and Toxicology, University of Veterinary Medicine, 1210 Vienna, Austria. Agnieszka.Witalisz-Siepracka@vetmeduni.ac.at.
Veronika SexlInstitute of Pharmacology and Toxicology, University of Veterinary Medicine, 1210 Vienna, Austria. veronika.sexl@vetmeduni.ac.at.
University of Veterinary Medicine Vienna · AT

Funding

Austrian Science Fund P28571-B21 to V.S.Austrian Science Fund SFB 4701, F4706-B20 to V.S.Austrian Science Fund SFB6107 to V.S.Austrian Science Fund FWF P 28571
6 · The paper itself

Abstract

Improvements in cancer therapy frequently stem from the development of new small-molecule inhibitors, paralleled by the identification of biomarkers that can predict the treatment response. Recent evidence supports the idea that cyclin-dependent kinase 8 (CDK8) may represent a potential drug target for breast and prostate cancer, although no CDK8 inhibitors have entered the clinics. As the available inhibitors have been recently reviewed, we focus on the biological functions of CDK8 and provide an overview of the complexity of CDK8-dependent signaling throughout evolution and CDK8-dependent effects that may open novel treatment avenues.

Indexed as

cancerCDK8mediator complex

Identifiers

PMID31248103
PMCPMC6630639
OpenAlexW2950285881

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.