Evidence map›Paper›PMID 22751009›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2012

Aurora B is regulated by acetylation/deacetylation during mitosis in prostate cancer cells.

Maria Fadri-Moskwik, Kimberly N Weiderhold, Arpaporn Deeraksa, Carol Chuang, Jing Pan, Sue-Hwa Lin, Li-Yuan Yu-Lee

Abstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-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

22 citing papers in PubMed, 36 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

7 authors at 2 institutions in 1 country.

Maria Fadri-MoskwikDepartment of Medicine-IAR Section, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.
Kimberly N Weiderhold
Arpaporn Deeraksa
Carol Chuang
Jing Pan
Sue-Hwa Lin
Li-Yuan Yu-Lee
Baylor College of Medicine · USThe University of Texas MD Anderson Cancer Center · US

Funding

Research Education and Career Horizons ProgramK12GM084897 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI SIFERS, RICHARD NORMAN, SLAUGHTER, GAYLE · 2008 to 2016
$8.3M
TSLP Signaling in Dendritic Cells - Aim 3U19AI071130 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DONG, CHEN · 2006 to 2010
$6.1M
TRAINING PROGRAM IN MOLECULAR ENDOCRINOLOGYT32DK007696 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI MOORE, DAVID D · 1993 to 2012
$2.8M
MOLECULAR AND CELLULAR MECHANISMS OF HOST DEFENSET32AI007495 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI TAN, TSE-HUA · 1996 to 2011
$2.4M
GENE SEQUENCES INVOLVED IN PROLACTIN ACTIONR01DK053176 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI YU-LEE, LI-YUAN · 1998 to 2007
$1.7M
Bone Metastasis Factor-1 in Prostate Cancer/Bone InteractionR01CA111479 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, SUE-HWA · 2005 to 2009
$1.3M
Function of NudC, a Novel Subtrate of Aurora B, in Spindle Checkpoint ActivityF31GM084695 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI WEIDERHOLD, KIMBERLY NICOLE · 2008 to 2011
$137k
NCI NIH HHS CA111479NCI NIH HHS R01 CA111479NIAID NIH HHS AI071130NIAID NIH HHS T32 AI007495NIAID NIH HHS T32-AI07495NIAID NIH HHS U19 AI071130NIDDK NIH HHS DK53176NIDDK NIH HHS R01 DK053176NIDDK NIH HHS T32 DK007696NIDDK NIH HHS T32-DK07696NIGMS NIH HHS F31 GM084695NIGMS NIH HHS F31-GM084695NIGMS NIH HHS K12 GM084897NIGMS NIH HHS K12-GM084897
6 · The paper itself

Abstract

Protein acetylation has been implicated in playing an important role during mitotic progression. Aurora B kinase is known to play a critical role in mitosis. However, whether Aurora B is regulated by acetylation is not known. Using IP with an anti-acetyl lysine antibody, we identified Aurora B as an acetylated protein in PC3 prostate cancer cells. Knockdown of HDAC3 or inhibiting HDAC3 deacetylase activity led to a significant increase (P<0.01 and P<0.05, respectively) in Aurora B acetylation as compared to siLuc or vehicle-treated controls. Increased Aurora B acetylation is correlated with a 30% reduction in Aurora B kinase activity in vitro and resulted in significant defects in Aurora B-dependent mitotic processes, including kinetochore-microtubule attachment and chromosome congression. Furthermore, Aurora B transiently interacts with HDAC3 at the kinetochore-microtubule interface of congressing chromosomes during prometaphase. This window of interaction corresponded with a transient but significant reduction (P=0.02) in Aurora B acetylation during early mitosis. Together, these results indicate that Aurora B is more active in its deacetylated state and further suggest a new mechanism by which dynamic acetylation/deacetylation acts as a rheostat to fine-tune Aurora B activity during mitotic progression.

Indexed as

AcetylationAurora Kinase BAurora KinasesCell Line, TumorHistone Deacetylase 3Histone DeacetylasesHumansImmunoblottingKinetochoresMaleMicroscopy, FluorescenceMicrotubulesMitosisProstatic NeoplasmsProtein Processing, Post-TranslationalProtein Serine-Threonine KinasesAURKB protein, humanAurora Kinase BAurora KinasesHistone Deacetylase 3Histone DeacetylasesProtein Serine-Threonine Kinases

Identifiers

PMID22751009
PMCPMC3448774
OpenAlexW2155476061

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.