Evidence map›Paper›PMID 29568371›Full record

ArticleOncotarget2018

CDK8/19 inhibition induces premature G1/S transition and ATR-dependent cell death in prostate cancer cells.

Akito Nakamura, Daisuke Nakata, Yuichi Kakoi, Mihoko Kunitomo, Saomi Murai, Shunsuke Ebara, Akito Hata, Takahito Hara

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

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  13. Cyclin-dependent kinases: Masters of the eukaryotic universe.Wiley interdisciplinary reviews. RNA · 2023
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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

8 authors at 1 institution in 1 country.

Akito NakamuraOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Daisuke NakataOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Yuichi KakoiOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Mihoko KunitomoOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Saomi MuraiOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Shunsuke EbaraOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Akito HataBio Molecular Research Laboratories, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Takahito HaraOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Takeda (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CDK8/19 kinase module comprises a subcomplex that interacts with the Mediator complex and regulates gene expression through phosphorylation of transcription factors and Mediator subunits. Mediator complex subunits have been increasingly implicated in cancer and other diseases. Although high expression of CDK8/19 has been demonstrated in prostate cancer, its function has not been thoroughly examined. Here we report that CDK8/19 modulates the gene expression of cell cycle regulators and thereby maintains the proper G1/S transition in prostate cancer cells. We show that highly selective CDK8/19 inhibitors exerted anti-proliferative activity in prostate cancer cells both

Indexed as

ATRCDK19CDK8cell cycleprostate cancer

Identifiers

PMID29568371
PMCPMC5862592
OpenAlexW2791080518

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.