Evidence map›Paper›PMID 30135207›Full record

ArticleThe Journal of biological chemistry2018

The tyrosine kinase v-Src causes mitotic slippage by phosphorylating an inhibitory tyrosine residue of Cdk1.

Maria Horiuchi, Takahisa Kuga, Youhei Saito, Maiko Nagano, Jun Adachi, Takeshi Tomonaga, Naoto Yamaguchi, Yuji Nakayama

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

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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 3 institutions in 1 country.

Maria HoriuchiFrom the Department of Biochemistry and Molecular Biology, Kyoto Pharmaceutical University, Kyoto 607-8414.
Takahisa KugaFrom the Department of Biochemistry and Molecular Biology, Kyoto Pharmaceutical University, Kyoto 607-8414.
Youhei SaitoFrom the Department of Biochemistry and Molecular Biology, Kyoto Pharmaceutical University, Kyoto 607-8414.ORCID 0000-0002-8545-6925
Maiko Naganothe Laboratory of Proteome Research, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka 567-0085, and.
Jun Adachithe Laboratory of Proteome Research, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka 567-0085, and.
Takeshi Tomonagathe Laboratory of Proteome Research, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka 567-0085, and.
Naoto Yamaguchithe Laboratory of Molecular Cell Biology, Graduate School of Pharmaceutical Sciences, Chiba University, Chiba 260-8675, Japan.
Yuji NakayamaFrom the Department of Biochemistry and Molecular Biology, Kyoto Pharmaceutical University, Kyoto 607-8414, nakayama@mb.kyoto-phu.ac.jp.ORCID 0000-0001-7882-0066
Kyoto Pharmaceutical University · JPNational Institute of Biomedical Innovation, Health and Nutrition · JPChiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nonreceptor tyrosine kinase v-Src is an oncogene first identified in Rous sarcoma virus. The oncogenic effects of v-Src have been intensively studied; however, its effects on chromosomal integrity are not fully understood. Here, using HeLa S3/v-Src cells having inducible v-Src expression, we found that v-Src causes mitotic slippage in addition to cytokinesis failure, even when the spindle assembly checkpoint is not satisfied because of the presence of microtubule-targeting agents. v-Src's effect on mitotic slippage was also observed in cells after a knockdown of C-terminal Src kinase (Csk), a protein-tyrosine kinase that inhibits Src-family kinases and was partially inhibited by PP2, an Src-family kinase inhibitor. Proteomic analysis and

Indexed as

Antineoplastic Agents, PhytogenicCDC2 Protein KinaseCell ProliferationHeLa CellsHumansMicrotubulesMitosisOncogene Protein pp60(v-src)PaclitaxelPhosphoproteinsPhosphorylationPolyploidyProtein Kinase InhibitorsPyrimidinesRNA, Small InterferingTime-Lapse ImagingAG 1879Antineoplastic Agents, PhytogenicCDC2 Protein KinaseCDK1 protein, humanOncogene Protein pp60(v-src)PaclitaxelPhosphoproteinsProtein Kinase InhibitorsPyrimidinesRNA, Small InterferingcancerCdk1cell cyclecyclin-dependent kinase (CDK)microtubule-targeting agentmitosismitotic slippagephosphorylationpTyr-15spindle checkpointSrctyrosine kinasev-Src

Identifiers

PMID30135207
PMCPMC6177586
OpenAlexW2888206600

What OpenQuestion holds

Textmetadata
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.