Evidence map›Paper›PMID 22864622›Full record

ReviewCellular and molecular life sciences : CMLS2013

Aurora A kinase (AURKA) in normal and pathological cell division.

Anna S Nikonova, Igor Astsaturov, Ilya G Serebriiskii, Roland L Dunbrack, Erica A Golemis

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 276 papers.

0numbers the graph read from it
0cells of the map it votes in
276citing papers in PubMed
11.5field-weighted citation impact, top 1% 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

276 citing papers in PubMed, 446 citations in OpenAlex.

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  19. Covalent Reprogramming of Kinase Binders to Modulate Protein Abundance.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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216 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Anna S NikonovaProgram in Developmental Therapeutics, Fox Chase Cancer Center, W406, 333 Cottman Ave., Philadelphia, PA 19111, USA.
Igor Astsaturov
Ilya G Serebriiskii
Roland L Dunbrack
Erica A Golemis
Fox Chase Cancer Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
ROLES OF HEF1 IN CELL DIFFERENTIATION AND SURVIVALR01CA063366 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GOLEMIS, ERICA A. · 1998 to 2013
$3.9M
Bayesian Statistics and Algorithms for Homology ModelingR01GM084453 · NIGMS · RESEARCH INST OF FOX CHASE CAN CTR · PI DUNBRACK, ROLAND L · 2008 to 2016
$2.6M
Cas Protein Regulation of EMT in CancerR01CA113342 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GOLEMIS, ERICA A. · 2007 to 2011
$1.5M
Targeting Sterol Gene SC4MOL and EGFR as Synergistic Anti-Cancer StrategyK22CA160725 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI ASTSATUROV, IGOR · 2011 to 2013
$592k
Regulation of EGFR by SC4MOL- and NSDHL-Dependent TraffickingR21CA164205 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI ASTSATUROV, IGOR · 2012 to 2013
$413k
NCI NIH HHS 1K22CA-160725NCI NIH HHS CA-06927NCI NIH HHS K22 CA160725NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA063366NCI NIH HHS R01 CA113342NCI NIH HHS R01 CA63366NCI NIH HHS R21 CA-164205NCI NIH HHS R21 CA164205NIGMS NIH HHS R01 GM084453NIGMS NIH HHS R01 GM84453
6 · The paper itself

Abstract

Temporally and spatially controlled activation of the Aurora A kinase (AURKA) regulates centrosome maturation, entry into mitosis, formation and function of the bipolar spindle, and cytokinesis. Genetic amplification and mRNA and protein overexpression of Aurora A are common in many types of solid tumor, and associated with aneuploidy, supernumerary centrosomes, defective mitotic spindles, and resistance to apoptosis. These properties have led Aurora A to be considered a high-value target for development of cancer therapeutics, with multiple agents currently in early-phase clinical trials. More recently, identification of additional, non-mitotic functions and means of activation of Aurora A during interphase neurite elongation and ciliary resorption have significantly expanded our understanding of its function, and may offer insights into the clinical performance of Aurora A inhibitors. Here we review the mitotic and non-mitotic functions of Aurora A, discuss Aurora A regulation in the context of protein structural information, and evaluate progress in understanding and inhibiting Aurora A in cancer.

Indexed as

Cell DivisionAnimalsAurora Kinase AAurora KinasesEnzyme ActivationEnzyme InhibitorsGene Expression Regulation, NeoplasticHumansModels, MolecularNeoplasmsProtein ConformationProtein Interaction MapsProtein Serine-Threonine KinasesAURKA protein, humanAurora Kinase AAurora KinasesEnzyme InhibitorsProtein Serine-Threonine Kinases

Identifiers

PMID22864622
PMCPMC3607959
OpenAlexW2083352151

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.