Evidence map›Paper›PMID 25205104›Full record

ArticleCancer research2014

PCTAIRE1 phosphorylates p27 and regulates mitosis in cancer cells.

Teruki Yanagi, Maryla Krajewska, Shu-ichi Matsuzawa, John C Reed

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

36 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
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  7. Cyclin-dependent kinases: Masters of the eukaryotic universe.Wiley interdisciplinary reviews. RNA · 2023
    Review
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  10. Development ofFrontiers in pharmacology · 2023
    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

4 authors at 1 institution in 1 country.

Teruki YanagiSanford-Burnham Medical Research Institute, La Jolla, California.
Maryla KrajewskaSanford-Burnham Medical Research Institute, La Jolla, California.
Shu-ichi MatsuzawaSanford-Burnham Medical Research Institute, La Jolla, California. smatsuzawa@sanfordburnham.org reedoffice@sanfordburnham.org.
John C ReedSanford-Burnham Medical Research Institute, La Jolla, California. smatsuzawa@sanfordburnham.org reedoffice@sanfordburnham.org.
Sanford Burnham Prebys Medical Discovery Institute · US

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Michael Jackson · 1985 to 2026
$107.2M
Virulence Mechanisms of Viral Bcl-2 HomologsR01AI091967 · NIAID · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI MATSUZAWA, SHU-ICHI · 2011 to 2015
$2.4M
Novel Pathway Connecting p53 to beta-Catenin degradationR21CA107403 · NCI · BURNHAM INSTITUTE FOR MEDICAL RESEARCH · PI MATSUZAWA, SHU-ICHI · 2004 to 2005
$346k
NCI NIH HHS P30 CA030199NCI NIH HHS R21 CA107403NIAID NIH HHS R01 AI091967
6 · The paper itself

Abstract

PCTAIRE1 is distant relative of the cyclin-dependent kinase family that has been implicated in spermatogenesis and neuronal development, but it has not been studied in cancer. Here, we report that PCTAIRE1 is expressed in prostate, breast, and cervical cancer cells, where its RNAi-mediated silencing causes growth inhibition with aberrant mitosis due to defects in centrosome dynamics. PCTAIRE1 was not similarly involved in proliferation of nontransformed cells, including diploid human IMR-90 fibroblasts. Through yeast two-hybrid screening, we identified tumor suppressor p27 as a PCTAIRE1 interactor. In vitro kinase assays showed PCTAIRE1 phosphorylates p27 at Ser10. PCTAIRE1 silencing modulated Ser10 phosphorylation on p27 and led to its accumulation in cancer cells but not in nontransformed cells. In a mouse xenograft model of PPC1 prostate cancer, conditional silencing of PCTAIRE1 restored p27 protein expression and suppressed tumor growth. Mechanistic studies in HeLa cells showed that PCTAIRE1 phosphorylates p27 during the S and M phases of the cell cycle. Notably, p27 silencing was sufficient to rescue cells from mitotic arrest caused by PCTAIRE1 silencing. Clinically, PCTAIRE1 was highly expressed in primary breast and prostate tumors compared with adjacent normal epithelial tissues. Together our findings reveal an unexpected role for PCTAIRE1 in regulating p27 stability, mitosis, and tumor growth, suggesting PCTAIRE1 as a candidate cancer therapeutic target.

Indexed as

MitosisProtein Processing, Post-TranslationalAnimalsBreast NeoplasmsCell ProliferationCyclin-Dependent Kinase Inhibitor p27Cyclin-Dependent KinasesFemaleGene Knockdown TechniquesHEK293 CellsHeLa CellsHumansMaleMice, NudeNeoplasm TransplantationPhosphorylationCyclin-Dependent Kinase Inhibitor p27Cyclin-Dependent KinasesPCTAIRE-1 protein kinaseRNA, Small Interfering

Identifiers

PMID25205104
PMCPMC4199897
OpenAlexW2114235916

What OpenQuestion holds

Textmetadata
LicenceTDM
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.