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Keep Calm and Carry on with Extra Centrosomes

https://doi.org/10.3390/cancers14020442

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1097-0029(20000601)49:5<409::aid-jemt2>3.0.co;2-vopenalex-snapshot

Integrating centrosome structure with protein composition and function in animal cells

inferredcites →https://doi.org/10.1002/(sici)1097-0169(1999)42:1<60::aid-cm6>3.0.co;2-7openalex-snapshot

Role for microtubules in centrosome doubling in chinese hamster ovary cells

inferredcites →https://doi.org/10.1002/(sici)1098-2264(200003)27:3<332::aid-gcc15>3.0.co;2-kopenalex-snapshot

PRK, a cell cycle gene localized to 8p21, is downregulated in head and neck cancer

inferredcites →https://doi.org/10.1002/bies.10262openalex-snapshot

Tumor progression: Small GTPases and loss of cell–cell adhesion

inferredcites →https://doi.org/10.1002/cm.20368openalex-snapshot

Centriole assembly in CHO cells expressing Plk4/SAS6/SAS4 is similar to centriogenesis in ciliated epithelial cells

inferredcites →https://doi.org/10.1002/gcc.20094openalex-snapshot

Telomere‐mediated mitotic disturbances in immortalized ovarian epithelial cells reproduce chromosomal losses and breakpoints from ovarian carcinoma

inferredcites →https://doi.org/10.1002/gcc.20425openalex-snapshot

DNA repair pathways involved in anaphase bridge formation

inferredcites →https://doi.org/10.1002/hep.23467openalex-snapshot

Oncogenic and Tumor Suppressive Roles of Polo-Like Kinases in Human Hepatocellular Carcinoma

inferredcites →https://doi.org/10.1002/jcp.1041540302openalex-snapshot

Heat shock alters centrosome organization leading to mitotic dysfunction and cell death

inferredcites →https://doi.org/10.1007/s00018-002-8510-yopenalex-snapshot

Cyclin A in cell cycle control and cancer

inferredcites →https://doi.org/10.1007/s00428-005-1212-8openalex-snapshot

Polo-like kinase isoforms in breast cancer: expression patterns and prognostic implications

inferredcites →https://doi.org/10.1007/s00432-019-02994-0openalex-snapshot

PLK4: a promising target for cancer therapy

inferredcites →https://doi.org/10.1007/s10434-001-0729-6openalex-snapshot

Comparative Expression of the Mitotic Regulators SAK and PLK in Colorectal Cancer

inferredcites →https://doi.org/10.1007/s10555-008-9163-6openalex-snapshot

Centrosomes and cancer: how cancer cells divide with too many centrosomes

inferredcites →https://doi.org/10.1007/s10577-010-9179-yopenalex-snapshot

Chromosomes and cancer cells

inferredcites →https://doi.org/10.1007/s11033-014-3546-2openalex-snapshot

PLK4 overexpression and its effect on centrosome regulation and chromosome stability in human gastric cancer

inferredcites →https://doi.org/10.1016/0092-8674(95)90142-6openalex-snapshot

Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo

inferredcites →https://doi.org/10.1016/j.bbamcr.2014.04.021openalex-snapshot

TEIF associated centrosome activity is regulated by EGF/PI3K/Akt signaling

inferredcites →https://doi.org/10.1016/j.bbcan.2008.05.003openalex-snapshot

Merotelic kinetochore orientation, aneuploidy, and cancer

inferredcites →https://doi.org/10.1016/j.bbrc.2003.12.050openalex-snapshot

Cloning and enzymatic analysis of 22 novel human ubiquitin-specific proteases

inferredcites →https://doi.org/10.1016/j.canlet.2004.12.028openalex-snapshot

Centrosome amplification, chromosome instability and cancer development

inferredcites →https://doi.org/10.1016/j.canlet.2005.06.017openalex-snapshot

Nek2 kinase in chromosome instability and cancer

inferredcites →https://doi.org/10.1016/j.canlet.2016.07.004openalex-snapshot

Plk2 promotes tumor growth and inhibits apoptosis by targeting Fbxw7/Cyclin E in colorectal cancer

inferredcites →https://doi.org/10.1016/j.ccr.2006.12.003openalex-snapshot

Aneuploidy Acts Both Oncogenically and as a Tumor Suppressor

inferredcites →https://doi.org/10.1016/j.ccr.2014.05.006openalex-snapshot

Functional Characterization of CFI-400945, a Polo-like Kinase 4 Inhibitor, as a Potential Anticancer Agent

inferredcites →https://doi.org/10.1016/j.ccr.2014.07.017openalex-snapshot

Polo-like Kinase 4 Inhibition: A Strategy for Cancer Therapy?

inferredcites →https://doi.org/10.1016/j.ceb.2005.12.008openalex-snapshot

Controlling centrosome number: licenses and blocks

inferredcites →https://doi.org/10.1016/j.cell.2008.05.039openalex-snapshot

Centrosome Amplification Can Initiate Tumorigenesis in Flies

inferredcites →https://doi.org/10.1016/j.cell.2013.06.007openalex-snapshot

Catastrophic Nuclear Envelope Collapse in Cancer Cell Micronuclei

inferredcites →https://doi.org/10.1016/j.celrep.2013.08.005openalex-snapshot

LRRC45 Is a Centrosome Linker Component Required for Centrosome Cohesion

inferredcites →https://doi.org/10.1016/j.celrep.2017.08.005openalex-snapshot

Asymmetric Centriole Numbers at Spindle Poles Cause Chromosome Missegregation in Cancer

inferredcites →https://doi.org/10.1016/j.celrep.2018.05.030openalex-snapshot

Bimodal Binding of STIL to Plk4 Controls Proper Centriole Copy Number

inferredcites →https://doi.org/10.1016/j.chembiol.2013.09.012openalex-snapshot

Design, Synthesis, and Biological Evaluation of an Allosteric Inhibitor of HSET that Targets Cancer Cells with Supernumerary Centrosomes

inferredcites →https://doi.org/10.1016/j.copbio.2016.03.011openalex-snapshot

Centrosomal clustering contributes to chromosomal instability and cancer

inferredcites →https://doi.org/10.1016/j.cub.2006.03.056openalex-snapshot

HURP Is Part of a Ran-Dependent Complex Involved in Spindle Formation

inferredcites →https://doi.org/10.1016/j.cub.2009.05.016openalex-snapshot

Control of Centriole Length by CPAP and CP110

inferredcites →https://doi.org/10.1016/j.cub.2009.05.018openalex-snapshot

Overly Long Centrioles and Defective Cell Division upon Excess of the SAS-4-Related Protein CPAP

inferredcites →https://doi.org/10.1016/j.cub.2010.01.034openalex-snapshot

Mechanisms of Chromosomal Instability

inferredcites →https://doi.org/10.1016/j.cub.2011.05.032openalex-snapshot

Cohesion Fatigue Induces Chromatid Separation in Cells Delayed at Metaphase

inferredcites →https://doi.org/10.1016/j.cub.2011.05.047openalex-snapshot

Plk1 Controls the Nek2A-PP1γ Antagonism in Centrosome Disjunction

inferredcites →https://doi.org/10.1016/j.cub.2013.09.037openalex-snapshot

Regulation of Autophosphorylation Controls PLK4 Self-Destruction and Centriole Number

inferredcites →https://doi.org/10.1016/j.devcel.2006.09.012openalex-snapshot

Sealed with a Kiz: How Plk1 Ensures Spindle Pole Integrity

inferredcites →https://doi.org/10.1016/j.devcel.2007.02.015openalex-snapshot

Centrosomes Promote Timely Mitotic Entry in C. elegans Embryos

inferredcites →https://doi.org/10.1016/j.devcel.2007.07.002openalex-snapshot

Plk4-Induced Centriole Biogenesis in Human Cells

inferredcites →https://doi.org/10.1016/j.devcel.2007.07.004openalex-snapshot

Regulated HsSAS-6 Levels Ensure Formation of a Single Procentriole per Centriole during the Centrosome Duplication Cycle

inferredcites →https://doi.org/10.1016/j.devcel.2015.06.013openalex-snapshot

Direct Microtubule-Binding by Myosin-10 Orients Centrosomes toward Retraction Fibers and Subcortical Actin Clouds

inferredcites →https://doi.org/10.1016/j.devcel.2016.12.022openalex-snapshot

Centrosome Amplification Is Sufficient to Promote Spontaneous Tumorigenesis in Mammals

inferredcites →https://doi.org/10.1016/j.devcel.2018.10.026openalex-snapshot

Oxidative Stress in Cells with Extra Centrosomes Drives Non-Cell-Autonomous Invasion

inferredcites →https://doi.org/10.1016/j.drudis.2019.05.024openalex-snapshot

Cancer cell fusion: a potential target to tackle drug-resistant and metastatic cancer cells

inferredcites →https://doi.org/10.1016/j.molcel.2005.02.014openalex-snapshot

A Role for PML3 in Centrosome Duplication and Genome Stability

inferredcites →https://doi.org/10.1016/j.molonc.2011.05.003openalex-snapshot

Centrosome clustering and chromosomal (in)stability: A matter of life and death

inferredcites →https://doi.org/10.1016/j.neo.2018.01.004openalex-snapshot

Plk2 Loss Commonly Occurs in Colorectal Carcinomas but not Adenomas: Relationship to mTOR Signaling

inferredcites →https://doi.org/10.1016/j.tcb.2009.04.001openalex-snapshot

Centrosome function in cancer: guilty or innocent?

inferredcites →https://doi.org/10.1016/j.yexcr.2009.12.007openalex-snapshot

The human IFN-inducible p53 target gene TRIM22 colocalizes with the centrosome independently of cell cycle phase

inferredcites →https://doi.org/10.1016/s0092-8674(00)00093-3openalex-snapshot

Nucleophosmin/B23 Is a Target of CDK2/Cyclin E in Centrosome Duplication

inferredcites →https://doi.org/10.1016/s0960-9822(99)80191-2openalex-snapshot

Cyclin-dependent kinase 2 (Cdk2) is required for centrosome duplication in mammalian cells

inferredcites →https://doi.org/10.1016/s0962-8924(02)02276-6openalex-snapshot

The awesome power of multiple model systems: interpreting the complex nature of spindle checkpoint signaling

inferredcites →https://doi.org/10.1016/s1097-2765(00)80466-9openalex-snapshot

Centrosome Amplification and a Defective G2–M Cell Cycle Checkpoint Induce Genetic Instability in BRCA1 Exon 11 Isoform–Deficient Cells

inferredcites →https://doi.org/10.1021/cb400186wopenalex-snapshot

Discovery and Mechanistic Study of a Small Molecule Inhibitor for Motor Protein KIFC1

inferredcites →https://doi.org/10.1023/a:1016550619925openalex-snapshot

Amplified Centrosomes in Breast Cancer: A Potential Indicator of Tumor Aggressiveness

inferredcites →https://doi.org/10.1023/b:jomg.0000048774.27697.30openalex-snapshot

Centrosome Amplification and the Origin of Chromosomal Instability in Breast Cancer

inferredcites →https://doi.org/10.1038/10054openalex-snapshot

Centrosome duplication in mammalian somatic cells requires E2F and Cdk2–Cyclin A

inferredcites →https://doi.org/10.1038/13802openalex-snapshot

Genomic instability in Gadd45a-deficient mice

inferredcites →https://doi.org/10.1038/2496openalex-snapshot

Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation

inferredcites →https://doi.org/10.1038/38291openalex-snapshot

Arrest of the cell cycle by the tumour-suppressor BRCA1 requires the CDK-inhibitor p21WAF1/CiPl

inferredcites →https://doi.org/10.1038/cddis.2017.167openalex-snapshot

Hepatocyte polyploidization and its association with pathophysiological processes

inferredcites →https://doi.org/10.1038/emboj.2010.230openalex-snapshot

CLASP1, astrin and Kif2b form a molecular switch that regulates kinetochore‐microtubule dynamics to promote mitotic progression and fidelity

inferredcites →https://doi.org/10.1038/emboj.2011.63openalex-snapshot

Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods

inferredcites →https://doi.org/10.1038/nature02166openalex-snapshot

Proteomic characterization of the human centrosome by protein correlation profiling

inferredcites →https://doi.org/10.1038/nature04217openalex-snapshot

Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells

inferredcites →https://doi.org/10.1038/nature04985openalex-snapshot

Mechanism limiting centrosome duplication to once per cell cycle

inferredcites →https://doi.org/10.1038/nature05318openalex-snapshot

Centriole assembly in Caenorhabditis elegans

inferredcites →https://doi.org/10.1038/nature08136openalex-snapshot

A mechanism linking extra centrosomes to chromosomal instability

inferredcites →https://doi.org/10.1038/nature10802openalex-snapshot

DNA breaks and chromosome pulverization from errors in mitosis

inferredcites →https://doi.org/10.1038/nature13277openalex-snapshot

Oncogene-like induction of cellular invasion from centrosome amplification

inferredcites →https://doi.org/10.1038/ncb1006-1050openalex-snapshot

Kizuna takes pole position

inferredcites →https://doi.org/10.1038/ncb1320openalex-snapshot

The Polo kinase Plk4 functions in centriole duplication

inferredcites →https://doi.org/10.1038/ncb1474openalex-snapshot

The Plk1 target Kizuna stabilizes mitotic centrosomes to ensure spindle bipolarity

inferredcites →https://doi.org/10.1038/ncb2423openalex-snapshot

CLASPs prevent irreversible multipolarity by ensuring spindle-pole resistance to traction forces during chromosome alignment

inferredcites →https://doi.org/10.1038/ncb2746openalex-snapshot

Centrosome amplification causes microcephaly

inferredcites →https://doi.org/10.1038/ncb2958openalex-snapshot

Mitotic spindle multipolarity without centrosome amplification

inferredcites →https://doi.org/10.1038/ncb3270openalex-snapshot

Transient PLK4 overexpression accelerates tumorigenesis in p53-deficient epidermis

inferredcites →https://doi.org/10.1038/ncb3370openalex-snapshot

Cilium assembly and disassembly

inferredcites →https://doi.org/10.1038/ncomms11005openalex-snapshot

A CEP215–HSET complex links centrosomes with spindle poles and drives centrosome clustering in cancer

inferredcites →https://doi.org/10.1038/ncomms15803openalex-snapshot

Precocious centriole disengagement and centrosome fragmentation induced by mitotic delay

inferredcites →https://doi.org/10.1038/ncomms6267openalex-snapshot

Direct interaction of Plk4 with STIL ensures formation of a single procentriole per parental centriole

inferredcites →https://doi.org/10.1038/ng1279openalex-snapshot

Phosphorylation by aurora kinase A induces Mdm2-mediated destabilization and inhibition of p53

inferredcites →https://doi.org/10.1038/nrc2249openalex-snapshot

Oncogenes and tumour suppressors take on centrosomes

inferredcites →https://doi.org/10.1038/nrc2781openalex-snapshot

Mitotic chromosomal instability and cancer: mouse modelling of the human disease

inferredcites →https://doi.org/10.1038/nrc924openalex-snapshot

Centrosome aberrations: cause or consequence of cancer progression?

inferredcites →https://doi.org/10.1038/nrm1276openalex-snapshot

From polyploidy to aneuploidy, genome instability and cancer

inferredcites →https://doi.org/10.1038/nrm2163openalex-snapshot

The spindle-assembly checkpoint in space and time

inferredcites →https://doi.org/10.1038/nrm2180openalex-snapshot

Centrosome biogenesis and function: centrosomics brings new understanding

inferredcites →https://doi.org/10.1038/nrm3474openalex-snapshot

The chromosomal passenger complex (CPC): from easy rider to the godfather of mitosis

inferredcites →https://doi.org/10.1038/nrm3819openalex-snapshot

Polo-like kinases: structural variations lead to multiple functions

inferredcites →https://doi.org/10.1038/nrm4062openalex-snapshot

Centrosome function and assembly in animal cells

inferredcites →https://doi.org/10.1038/nsmb.2846openalex-snapshot

Molecular basis for unidirectional scaffold switching of human Plk4 in centriole biogenesis

inferredcites →https://doi.org/10.1038/onc.2008.252openalex-snapshot

Aurora-A and ch-TOG act in a common pathway in control of spindle pole integrity

inferredcites →https://doi.org/10.1038/onc.2008.503openalex-snapshot

Localization of TEIF in the centrosome and its functional association with centrosome amplification in DNA damage, telomere dysfunction and human cancers

inferredcites →https://doi.org/10.1038/onc.2010.253openalex-snapshot

The Ras oncogene signals centrosome amplification in mammary epithelial cells through cyclin D1/Cdk4 and Nek2

inferredcites →https://doi.org/10.1038/onc.2010.431openalex-snapshot

A critical role of integrin-linked kinase, ch-TOG and TACC3 in centrosome clustering in cancer cells

inferredcites →https://doi.org/10.1038/onc.2015.105openalex-snapshot

The role of Plk3 in oncogenesis

inferredcites →https://doi.org/10.1038/s41419-017-0088-2openalex-snapshot

Polo-like kinase 4 mediates epithelial–mesenchymal transition in neuroblastoma via PI3K/Akt signaling pathway

inferredcites →https://doi.org/10.1038/s41467-018-03283-zopenalex-snapshot

Integrated genomics and functional validation identifies malignant cell specific dependencies in triple negative breast cancer

inferredcites →https://doi.org/10.1038/s41467-018-03641-xopenalex-snapshot

Over-elongation of centrioles in cancer promotes centriole amplification and chromosome missegregation

inferredcites →https://doi.org/10.1038/s41467-018-05429-5openalex-snapshot

Plk1 overexpression induces chromosomal instability and suppresses tumor development

inferredcites →https://doi.org/10.1038/s41467-019-11584-0openalex-snapshot

Mild replication stress causes chromosome mis-segregation via premature centriole disengagement

inferredcites →https://doi.org/10.1038/s41467-020-20208-xopenalex-snapshot

The ATM and ATR kinases regulate centrosome clustering and tumor recurrence by targeting KIFC1 phosphorylation

inferredcites →https://doi.org/10.1038/s41568-018-0084-6openalex-snapshot

Cytokinesis defects and cancer

inferredcites →https://doi.org/10.1038/s41586-020-2710-1openalex-snapshot

TRIM37 controls cancer-specific vulnerability to PLK4 inhibition

inferredcites →https://doi.org/10.1038/sj.bjc.6600438openalex-snapshot

Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres

inferredcites →https://doi.org/10.1038/sj.bjc.6601610openalex-snapshot

Polo-like kinase isoform expression is a prognostic factor in ovarian carcinoma

inferredcites →https://doi.org/10.1038/sj.bjc.6601803openalex-snapshot

Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas

inferredcites →https://doi.org/10.1038/sj.leu.2403779openalex-snapshot

Centrosome aberrations in chronic myeloid leukemia correlate with stage of disease and chromosomal instability

inferredcites →https://doi.org/10.1038/sj.onc.1200862openalex-snapshot

Prognostic significance of polo-like kinase (PLK) expression in non-small cell lung cancer

inferredcites →https://doi.org/10.1038/sj.onc.1203460openalex-snapshot

Synergistic induction of centrosome hyperamplification by loss of p53 and cyclin E overexpression

inferredcites →https://doi.org/10.1038/sj.onc.1204424openalex-snapshot

Direct regulation of the centrosome duplication cycle by the p53-p21Waf1/Cip1 pathway

inferredcites →https://doi.org/10.1038/sj.onc.1205707openalex-snapshot

Loss of p53 and centrosome hyperamplification

inferredcites →https://doi.org/10.1038/sj.onc.1208273openalex-snapshot

Polo-like kinases and oncogenesis

inferredcites →https://doi.org/10.1038/sj.onc.1210085openalex-snapshot

Direct evidence for the role of centrosomally localized p53 in the regulation of centrosome duplication

inferredcites →https://doi.org/10.1038/sj.onc.1210804openalex-snapshot

Ubiquitylated Tax targets and binds the IKK signalosome at the centrosome

inferredcites →https://doi.org/10.1042/bj20150992openalex-snapshot

Discovery of a novel inhibitor of kinesin-like protein KIFC1

inferredcites →https://doi.org/10.1042/bst20160116openalex-snapshot

The PLK4–STIL–SAS-6 module at the core of centriole duplication

inferredcites →https://doi.org/10.1042/bst20170087openalex-snapshot

Regulation of the cell cycle and centrosome biology by deubiquitylases

inferredcites →https://doi.org/10.1042/bst20190034openalex-snapshot

Targeting centrosome amplification, an Achilles' heel of cancer

inferredcites →https://doi.org/10.1073/pnas.0900108106openalex-snapshot

Efficient acquisition of dual metastasis organotropism to bone and lung through stable spontaneous fusion between MDA-MB-231 variants

inferredcites →https://doi.org/10.1073/pnas.0901587106openalex-snapshot

The augmin complex plays a critical role in spindle microtubule generation for mitotic progression and cytokinesis in human cells

inferredcites →https://doi.org/10.1073/pnas.132269599openalex-snapshot

Activation of Cdc2/cyclin B and inhibition of centrosome amplification in cells depleted of Plk1 by siRNA

inferredcites →https://doi.org/10.1073/pnas.1503683112openalex-snapshot

NDRG1 links p53 with proliferation-mediated centrosome homeostasis and genome stability

inferredcites →https://doi.org/10.1073/pnas.152205299openalex-snapshot

Multiple centrosomes arise from tetraploidy checkpoint failure and mitotic centrosome clusters in p53 and RB pocket protein-compromised cells

inferredcites →https://doi.org/10.1073/pnas.1716840115openalex-snapshot

STED nanoscopy of the centrosome linker reveals a CEP68-organized, periodic rootletin network anchored to a C-Nap1 ring at centrioles

inferredcites →https://doi.org/10.1073/pnas.1719760115openalex-snapshot

Polo-like kinase 4 inhibition produces polyploidy and apoptotic death of lung cancers

inferredcites →https://doi.org/10.1073/pnas.1813310115openalex-snapshot

CFI-400945 is not a selective cellular PLK4 inhibitor

inferredcites →https://doi.org/10.1073/pnas.1813967115openalex-snapshot

Reply to Oegema et al.: CFI-400945 and Polo-like kinase 4 inhibition

inferredcites →https://doi.org/10.1073/pnas.25.8.405openalex-snapshot

The Behavior in Successive Nuclear Divisions of a Chromosome Broken at Meiosis

inferredcites →https://doi.org/10.1073/pnas.96.6.2817openalex-snapshot

Cyclin-dependent kinase control of centrosome duplication

inferredcites →https://doi.org/10.1074/jbc.m003839200openalex-snapshot

Characterization of p190RhoGEF, A RhoA-specific Guanine Nucleotide Exchange Factor That Interacts with Microtubules

inferredcites →https://doi.org/10.1074/jbc.m009528200openalex-snapshot

p53 Displacement from Centrosomes and p53-mediated G1 Arrest following Transient Inhibition of the Mitotic Spindle

inferredcites →https://doi.org/10.1074/jbc.m314182200openalex-snapshot

Polo-like Kinase 1 (Plk1) Inhibits p53 Function by Physical Interaction and Phosphorylation

inferredcites →https://doi.org/10.1074/jbc.m400781200openalex-snapshot

Function of Drg1/Rit42 in p53-dependent Mitotic Spindle Checkpoint

inferredcites →https://doi.org/10.1083/jcb.141.7.1563openalex-snapshot

C-Nap1, a Novel Centrosomal Coiled-Coil Protein and Candidate Substrate of the Cell Cycle–regulated Protein Kinase Nek2

inferredcites →https://doi.org/10.1083/jcb.147.5.969openalex-snapshot

Centriolar Satellites

inferredcites →https://doi.org/10.1083/jcb.151.4.837openalex-snapshot

The Centrosomal Protein C-Nap1 Is Required for Cell Cycle–Regulated Centrosome Cohesion

inferredcites →https://doi.org/10.1083/jcb.200204023openalex-snapshot

Assembly of centrosomal proteins and microtubule organization depends on PCM-1

inferredcites →https://doi.org/10.1083/jcb.200504107openalex-snapshot

Rootletin forms centriole-associated filaments and functions in centrosome cohesion

inferredcites →https://doi.org/10.1083/jcb.200506119openalex-snapshot

Separase: a universal trigger for sister chromatid disjunction but not chromosome cycle progression

inferredcites →https://doi.org/10.1083/jcb.200701163openalex-snapshot

Astrin is required for the maintenance of sister chromatid cohesion and centrosome integrity

inferredcites →https://doi.org/10.1083/jcb.200710074openalex-snapshot

Integrin-linked kinase localizes to the centrosome and regulates mitotic spindle organization

inferredcites →https://doi.org/10.1083/jcb.200906019openalex-snapshot

Centrosomal Aki1 and cohesin function in separase-regulated centriole disengagement

inferredcites →https://doi.org/10.1083/jcb.201005065openalex-snapshot

HURP permits MTOC sorting for robust meiotic spindle bipolarity, similar to extra centrosome clustering in cancer cells

inferredcites →https://doi.org/10.1083/jcb.201006049openalex-snapshot

Cep152 interacts with Plk4 and is required for centriole duplication

inferredcites →https://doi.org/10.1083/jcb.201101073openalex-snapshot

Repeated cleavage failure does not establish centrosome amplification in untransformed human cells

inferredcites →https://doi.org/10.1083/jcb.201108006openalex-snapshot

Breaking the ties that bind: New advances in centrosome biology

inferredcites →https://doi.org/10.1083/jcb.201212060openalex-snapshot

CEP120 interacts with CPAP and positively regulates centriole elongation

inferredcites →https://doi.org/10.1083/jcb.201409151openalex-snapshot

Hsp72 is targeted to the mitotic spindle by Nek6 to promote K-fiber assembly and mitotic progression

inferredcites →https://doi.org/10.1083/jcb.201502088openalex-snapshot

Binding of STIL to Plk4 activates kinase activity to promote centriole assembly

inferredcites →https://doi.org/10.1083/jcb.201704102openalex-snapshot

Loss of E-cadherin provides tolerance to centrosome amplification in epithelial cancer cells

inferredcites →https://doi.org/10.1083/jcb.51.1.286openalex-snapshot

CENTRIOLE MORPHOGENESIS IN DEVELOPING CILIATED EPITHELIUM OF THE MOUSE OVIDUCT

inferredcites →https://doi.org/10.1083/jcb.58.1.96openalex-snapshot

NITROUS OXIDE: EFFECTS ON THE MITOTIC APPARATUS AND CHROMOSOME MOVEMENT IN H E L A CELLS

inferredcites →https://doi.org/10.1083/jcb.90.3.554openalex-snapshot

Tubulin assembly sites and the organization of cytoplasmic microtubules in cultured mammalian cells.

inferredcites →https://doi.org/10.1083/jcb.94.3.549openalex-snapshot

Mitosis in a cell with multiple centrioles.

inferredcites →https://doi.org/10.1091/mbc.e04-08-0688openalex-snapshot

Dynamic Recruitment of Nek2 Kinase to the Centrosome Involves Microtubules, PCM-1, and Localized Proteasomal Degradation

inferredcites →https://doi.org/10.1091/mbc.e05-10-0943openalex-snapshot

Rootletin Interacts with C-Nap1 and May Function as a Physical Linker between the Pair of Centrioles/Basal Bodies in Cells

inferredcites →https://doi.org/10.1091/mbc.e07-12-1269openalex-snapshot

GEF-H1 Couples Nocodazole-induced Microtubule Disassembly to Cell Contractility via RhoA

inferredcites →https://doi.org/10.1091/mbc.e09-06-0505openalex-snapshot

Autophosphorylation of Polo-like Kinase 4 and Its Role in Centriole Duplication

inferredcites →https://doi.org/10.1091/mbc.e09-12-1049openalex-snapshot

Daughter Centriole Elongation Is Controlled by Proteolysis

inferredcites →https://doi.org/10.1093/emboj/17.2.470openalex-snapshot

A centrosomal function for the human Nek2 protein kinase, a member of the NIMA family of cell cycle regulators

inferredcites →https://doi.org/10.1093/emboj/21.4.483openalex-snapshot

Aurora‐A overexpression reveals tetraploidization as a major route to centrosome amplification in p53−/− cells

inferredcites →https://doi.org/10.1093/jmcb/mjab041openalex-snapshot

Multifaceted roles of centrosomes in development, health, and disease

inferredcites →https://doi.org/10.1093/jmcb/mjq057openalex-snapshot

Genomic instability and cancer: an introduction

inferredcites →https://doi.org/10.1098/rsob.150209openalex-snapshot

Over-expression of Plk4 induces centrosome amplification, loss of primary cilia and associated tissue hyperplasia in the mouse

inferredcites →https://doi.org/10.1098/rstb.1990.0015openalex-snapshot

DNA methylation and epigenetic inheritance

inferredcites →https://doi.org/10.1098/rstb.2013.0467openalex-snapshot

Causes and consequences of centrosome abnormalities in cancer

inferredcites →https://doi.org/10.1101/gad.11.16.2101openalex-snapshot

The human papillomavirus E7 oncoprotein can uncouple cellular differentiation and proliferation in human keratinocytes by abrogating p21Cip1-mediated inhibition of cdk2

inferredcites →https://doi.org/10.1101/gad.13.12.1501openalex-snapshot

CDK inhibitors: positive and negative regulators of G1-phase progression

inferredcites →https://doi.org/10.1101/gad.1596308openalex-snapshot

β-Catenin is a Nek2 substrate involved in centrosome separation

inferredcites →https://doi.org/10.1101/gad.1700908openalex-snapshot

Mechanisms to suppress multipolar divisions in cancer cells with extra centrosomes

inferredcites →https://doi.org/10.1101/gad.207027.112openalex-snapshot

The autoregulated instability of Polo-like kinase 4 limits centrosome duplication to once per cell cycle

inferredcites →https://doi.org/10.1101/gad.439107openalex-snapshot

The nature of telomere fusion and a definition of the critical telomere length in human cells

inferredcites →https://doi.org/10.1111/j.1365-2443.2006.00990.xopenalex-snapshot

Mammalian CLASPs are required for mitotic spindle organization and kinetochore alignment

inferredcites →https://doi.org/10.1126/science.1104905openalex-snapshot

Spindle Multipolarity Is Prevented by Centrosomal Clustering

inferredcites →https://doi.org/10.1126/science.1209037openalex-snapshot

The Centrosome in Cells and Organisms

inferredcites →https://doi.org/10.1126/science.1210214openalex-snapshot

Chromosome Segregation Errors as a Cause of DNA Damage and Structural Chromosome Aberrations

inferredcites →https://doi.org/10.1126/science.271.5256.1744openalex-snapshot

Abnormal Centrosome Amplification in the Absence of p53

inferredcites →https://doi.org/10.1126/science.aaa5111openalex-snapshot

Reversible centriole depletion with an inhibitor of Polo-like kinase 4

inferredcites →https://doi.org/10.1126/scitranslmed.3000915openalex-snapshot

Proteins Required for Centrosome Clustering in Cancer Cells

inferredcites →https://doi.org/10.1128/mcb.00253-09openalex-snapshot

Cdk2 and Cdk4 Regulate the Centrosome Cycle and Are Critical Mediators of Centrosome Amplification in p53-Null Cells

inferredcites →https://doi.org/10.1128/mcb.01064-14openalex-snapshot

TRIM28 Is an E3 Ligase for ARF-Mediated NPM1/B23 SUMOylation That Represses Centrosome Amplification

inferredcites →https://doi.org/10.1155/2010/128478openalex-snapshot

The Enigma of Tripeptidyl-Peptidase II: Dual Roles in Housekeeping and Stress

inferredcites →https://doi.org/10.1155/2012/282430openalex-snapshot

Hepatocytes Polyploidization and Cell Cycle Control in Liver Physiopathology

inferredcites →https://doi.org/10.1158/0008-5472.can-03-3908openalex-snapshot

Induction of Centrosome Amplification and Chromosome Instability in Human Bladder Cancer Cells by p53 Mutation and Cyclin E Overexpression

inferredcites →https://doi.org/10.1158/0008-5472.can-04-2085openalex-snapshot

Mitotic Infidelity and Centrosome Duplication Errors in Cells Overexpressing Tripeptidyl-Peptidase II

inferredcites →https://doi.org/10.1158/0008-5472.can-06-1661openalex-snapshot

MYCN-Directed Centrosome Amplification Requires MDM2-Mediated Suppression of p53 Activity in Neuroblastoma Cells

inferredcites →https://doi.org/10.1158/0008-5472.can-07-0663openalex-snapshot

Identification of Griseofulvin as an Inhibitor of Centrosomal Clustering in a Phenotype-Based Screen

inferredcites →https://doi.org/10.1158/0008-5472.can-07-6182openalex-snapshot

Polo-like Kinase 3 Functions as a Tumor Suppressor and Is a Negative Regulator of Hypoxia-Inducible Factor-1α under Hypoxic Conditions

inferredcites →https://doi.org/10.1158/0008-5472.can-09-1284openalex-snapshot

Cullin 1 Functions as a Centrosomal Suppressor of Centriole Multiplication by Regulating Polo-like Kinase 4 Protein Levels

inferredcites →https://doi.org/10.1158/0008-5472.can-09-2159openalex-snapshot

Cell Fusion as a Hidden Force in Tumor Progression

inferredcites →https://doi.org/10.1158/0008-5472.can-12-2026openalex-snapshot

GF-15, a Novel Inhibitor of Centrosomal Clustering, Suppresses Tumor Cell Growth In Vitro and In Vivo

inferredcites →https://doi.org/10.1158/0008-5472.can-13-3398openalex-snapshot

Mechanisms Promoting Escape from Mitotic Stress–Induced Tumor Cell Death

inferredcites →https://doi.org/10.1158/0008-5472.can-14-1494openalex-snapshot

CDK2 Inhibition Causes Anaphase Catastrophe in Lung Cancer through the Centrosomal Protein CP110

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4635430openalex-extracted

Supernumerary Centrosome Promotes Glycogen Levels in Hepatocytes Via Metabolic Reprogramming in DEN/CCL4-Induced Mice

inferred← citeshttps://doi.org/10.1002/advs.202306318openalex-snapshot

Surviving the Storm: The Role of Poly‐ and Depolyploidization in Tissues and Tumors

inferred← citeshttps://doi.org/10.1002/advs.202501015openalex-snapshot

Chromosomal Instability Drives Glioblastoma Heterogeneity and Therapeutic Opportunities

inferred← citeshttps://doi.org/10.1002/cm.22004openalex-snapshot

Betrayal From the Core: Centriolar and Cytoskeletal Subversion by Infectious Pathogens

inferred← citeshttps://doi.org/10.1002/cmdc.202500426openalex-snapshot

Cytotoxicity of Atropisomeric [1,1′‐Binaphthalene]‐2,2′‐Diamines (BINAM) and Analogs in Human Cancer Cells: Enantioselectivity, Structure–Activity Relationships, and Mechanism

inferred← citeshttps://doi.org/10.1002/gcc.23096openalex-snapshot

Inactivation of RB1 , CDKN2A , and TP53 have distinct effects on genomic stability at side‐by‐side comparison in karyotypically normal cells

inferred← citeshttps://doi.org/10.1016/b978-0-12-821618-7.00231-5openalex-snapshot

Centrosomes and Centrioles

inferred← citeshttps://doi.org/10.1016/j.bioorg.2026.110130openalex-snapshot

Norlichexanthone, a shunt product of Griseofulvin, disrupts spindle assembly checkpoint and nucleocytoplasmic transport by targeting TPR in the nuclear pore complex

inferred← citeshttps://doi.org/10.1016/j.ceb.2025.102485openalex-snapshot

Centrosome biogenesis and maintenance in homeostasis and disease

inferred← citeshttps://doi.org/10.1016/j.semcancer.2025.01.008openalex-snapshot

Drivers of centrosome abnormalities: Senescence progression and tumor immune escape

inferred← citeshttps://doi.org/10.1038/s41418-023-01208-yopenalex-snapshot

Hornerin mediates phosphorylation of the polo-box domain in Plk1 by Chk1 to induce death in mitosis

inferred← citeshttps://doi.org/10.1038/s41419-024-06601-0openalex-snapshot

Nek2A prevents centrosome clustering and induces cell death in cancer cells via KIF2C interaction

inferred← citeshttps://doi.org/10.1038/s41598-024-53985-2openalex-snapshot

Prolonged overexpression of PLK4 leads to formation of centriole rosette clusters that are connected via canonical centrosome linker proteins

inferred← citeshttps://doi.org/10.1101/2023.10.10.561779openalex-snapshot

Prolonged over-expression of PLK4 amplifies centrosomes through formation of inter-connected centrosome rosette clusters

inferred← citeshttps://doi.org/10.1101/2024.02.09.579615openalex-snapshot

The cell cycle variant in multiciliated cells incorporates 2 centriole biogenesis cycles

inferred← citeshttps://doi.org/10.1101/2024.06.17.599429openalex-snapshot

Nucleolin acute degradation reveals novel functions in cell cycle progression and division in TNBC

inferred← citeshttps://doi.org/10.1111/febs.70240openalex-snapshot

Lysine demethylase 4A is a centrosome‐associated protein required for centrosome integrity and genomic stability

inferred← citeshttps://doi.org/10.1186/s12964-026-02865-5openalex-snapshot

Stress adaptation pathways and HA–CD44 signaling maintain the survival of pancreatic cancer cells with centrosome amplification

inferred← citeshttps://doi.org/10.2174/1389557522666220820113953openalex-snapshot

Centrosome Clustering & Chemotherapy

inferred← citeshttps://doi.org/10.3390/cancers14204986openalex-snapshot

Chromosomal Instability, Selection and Competition: Factors That Shape the Level of Karyotype Intra-Tumor Heterogeneity

inferred← citeshttps://doi.org/10.3390/cancers15010154openalex-snapshot

Centrosome Amplification Is a Potential Molecular Target in Paediatric Acute Lymphoblastic Leukemia

inferred← citeshttps://doi.org/10.3390/cells11152445openalex-snapshot

Duplication and Segregation of Centrosomes during Cell Division

inferred← citeshttps://doi.org/10.7554/elife.96584openalex-snapshot

The cell cycle variant in multiciliated cells incorporates 2 centriole biogenesis cycles

inferred← citeshttps://doi.org/10.7554/elife.96584.1openalex-snapshot

Microtubule-dependent orchestration of centriole amplification in brain multiciliated cells

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