Evidence map›Paper›PMID 31131319›Full record

ArticleScience advances2019

Molecular mechanism and potential target indication of TAK-931, a novel CDC7-selective inhibitor.

Kenichi Iwai, Tadahiro Nambu, Ryo Dairiki, Momoko Ohori, Jie Yu, Kristine Burke, Masamitsu Gotou, Yukiko Yamamoto, Shunsuke Ebara, Sachio Shibata and 14 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. CDC7 and APC/CNature communications · 2026
    Article
  3. Review
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  5. Article
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  11. A nucleosome switch primes Hepatitis B Virus infection.bioRxiv : the preprint server for biology · 2024
    Article
  12. Review
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  15. Article
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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

24 authors at 3 institutions in 2 countries.

Kenichi IwaiOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.ORCID 0000-0002-4127-8928
Tadahiro NambuOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.ORCID 0000-0002-5538-5214
Ryo DairikiOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Momoko OhoriOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Jie YuOncology Drug Discovery Unit, Takeda Pharmaceuticals International Co., Cambridge, MA, USA.ORCID 0000-0003-4423-1778
Kristine BurkeOncology Drug Discovery Unit, Takeda Pharmaceuticals International Co., Cambridge, MA, USA.ORCID 0000-0002-1334-3921
Masamitsu GotouIntegrated Research Laboratories, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Yukiko YamamotoOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Shunsuke EbaraOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.ORCID 0000-0001-6057-6173
Sachio ShibataOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.ORCID 0000-0002-0347-1911
Ryosuke HibinoOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Satoru NishizawaOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Tohru MiyazakiOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Misaki HommaOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Yuya OguroOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Takashi ImadaOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.ORCID 0000-0001-8139-8556
Nobuo ChoOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.ORCID 0000-0001-8561-8915
Noriko UchiyamaBiomolecular Research Laboratories, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Akifumi KogameDMPK Research Laboratories, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Toshiyuki TakeuchiDMPK Research Laboratories, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Osamu KurasawaOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.ORCID 0000-0001-5313-3753
Kazunori YamanakaIntegrated Research Laboratories, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.
Huifeng NiuTranslational and Biomarker Research, Takeda Pharmaceuticals International Co., Cambridge, MA, USA.ORCID 0000-0003-2181-7530
Akihiro OhashiOncology Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan.ORCID 0000-0002-4036-9385
Takeda (Japan) · JPTakeda (United States) · USChiba Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Replication stress (RS) is a cancer hallmark; chemotherapeutic drugs targeting RS are widely used as treatments for various cancers. To develop next-generation RS-inducing anticancer drugs, cell division cycle 7 (CDC7) has recently attracted attention as a target. We have developed an oral CDC7-selective inhibitor, TAK-931, as a candidate clinical anticancer drug. TAK-931 induced S phase delay and RS. TAK-931-induced RS caused mitotic aberrations through centrosome dysregulation and chromosome missegregation, resulting in irreversible antiproliferative effects in cancer cells. TAK-931 exhibited significant antiproliferative activity in preclinical animal models. Furthermore, in indication-seeking studies using large-scale cell panel data, TAK-931 exhibited higher antiproliferative activities in

Indexed as

AnimalsAntineoplastic AgentsCell Cycle ProteinsCell Line, TumorCell ProliferationCell SeparationCell SurvivalCentrosomeChromosome AberrationsComputational BiologyDrug Resistance, NeoplasmDrug Screening Assays, AntitumorFemaleHeLa CellsHumansInhibitory Concentration 50Antineoplastic AgentsCDC7 protein, humanCell Cycle ProteinsProtein Kinase InhibitorsProtein Serine-Threonine KinasesPyrazolonesPyrimidinessimurosertib

Identifiers

PMID31131319
PMCPMC6531005
OpenAlexW2945933050

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.