Evidence map›Paper›PMID 28739871›Full record

ArticleThe Journal of biological chemistry2017

Cyclin-dependent kinase 1 (CDK1)-mediated mitotic phosphorylation of the transcriptional co-repressor Vgll4 inhibits its tumor-suppressing activity.

Yongji Zeng, Seth Stauffer, Jiuli Zhou, Xingcheng Chen, Yuanhong Chen, Jixin Dong

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Zyxin promotes colon cancer tumorigenesis in a mitotic phosphorylation-dependent manner and through CDK8-mediated YAP activation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  10. Article
  11. Review
  12. 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

6 authors at 2 institutions in 1 country.

Yongji ZengFrom the Eppley Institute for Research in Cancer, Fred & Pamela Buffett Cancer Center.
Seth StaufferFrom the Eppley Institute for Research in Cancer, Fred & Pamela Buffett Cancer Center.
Jiuli ZhouFrom the Eppley Institute for Research in Cancer, Fred & Pamela Buffett Cancer Center.
Xingcheng ChenFrom the Eppley Institute for Research in Cancer, Fred & Pamela Buffett Cancer Center.
Yuanhong ChenFrom the Eppley Institute for Research in Cancer, Fred & Pamela Buffett Cancer Center.
Jixin DongFrom the Eppley Institute for Research in Cancer, Fred & Pamela Buffett Cancer Center, dongj@unmc.edu.
Fred and Pamela Buffett Cancer CenterSusan Thompson Buffett Foundation · US

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Research Pilot Project ProgramP30GM106397 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JOHNSON, KEITH R · 2013 to 2017
$4.9M
Regulation and Functional Dissection of YAP in MitosisR01GM109066 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DONG, JIXIN · 2014 to 2018
$1.4M
NCI NIH HHS P30 CA036727NIGMS NIH HHS P30 GM106397NIGMS NIH HHS R01 GM109066
6 · The paper itself

Abstract

The Hippo pathway is an evolutionarily conserved signaling pathway that plays important roles in stem cell biology, tissue homeostasis, and cancer development. Vestigial-like 4 (Vgll4) functions as a transcriptional co-repressor in the Hippo-Yes-associated protein (YAP) pathway. Vgll4 inhibits cell proliferation and tumor growth by competing with YAP for binding to TEA-domain proteins (TEADs). However, the mechanisms by which Vgll4 itself is regulated are unclear. Here we identified a mechanism that regulates Vgll4's tumor-suppressing function. We found that Vgll4 is phosphorylated

Indexed as

MitosisAnimalsCDC2 Protein KinaseCell ProliferationCells, CulturedCyclin-Dependent KinasesHumansMiceNeoplasms, ExperimentalPhosphorylationTranscription FactorsCDC2 Protein KinaseCDK1 protein, humanCyclin-Dependent KinasesTranscription FactorsVGLL4 protein, humancyclin-dependent kinase (CDK)Hippo pathwaymitosisphosphorylationtumor suppressor gene

Identifiers

PMID28739871
PMCPMC5592678
OpenAlexW2739405852

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.