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Polyploidy is a common outcome of chemotherapies, but there is conflicting evidence as to whether polyploidy is an adverse, benign or even favourable outcome. We show Aurora B kinase inhibitors efficiently promote polyploidy in many cell types, resulting in the cell cycle exit in RB and p53 functional cells, but hyper-polyploidy in cells with loss of RB and p53 function. These hyper-polyploid cells (>8n DNA content) are viable but have lost long-term proliferative potential in vitro and fail to form tumours in vivo. Investigation of mitosis in these cells revealed high numbers of centrosomes that were capable of supporting functional mitotic spindle poles, but these failed to progress to anaphase/telophase structures even when AURKB inhibitor was removed after 2-3 days. However, when AURKB inhibitor was removed after 1 day and cells had failed a single cytokinesis to become tetraploid, they retained colony forming ability and long-term proliferative potential. Mathematical modelling of the potential for polyploid cells to produce viable daughter cells demonstrated that cells with >8n DNA and >4 functional spindle poles approach zero probability of a viable daughter, supporting our experimental observations. These findings demonstrate that tetraploidy is tolerated by tumour cells, but higher ploidy states are incompatible with long-term proliferative potential. Model for AURKBi driven hyper-polyploid cells formation and fate. Aurora B inhibitor (AURKBi) treatment of RB+p53 defective cells efficiently promotes failed cell division. One failed cell division produces three possible outcomes, continued proliferation of the tetraploid daughter, cell death, or if AURKBi is continued, high polyploid states. Once cell have failed cell division >twice and have >8n DNA content they will continue to undergo rounds of endomitosis even in the absence of AURKBi to either become viable hyper-polyploid or die. The hyper-polyploid cells have no long-term proliferative potential.
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http://dx.doi.org/10.1038/s41419-024-07329-7 | DOI Listing |
Eur J Pharmacol
September 2025
Departamento de Química and Institute for advanced research in chemical Science (IAdChem), Facultad de Ciencias, Módulo 13, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
The Skp2-Cks1 protein-protein interaction (PPI) within the SCF ubiquitin ligase acts as a co-receptor for phosphorylated CDK inhibitors-most prominently p27-relieving CDK inhibition and advancing the cell cycle, a dependency accentuated in RB-pathway-defective cancers. Crystallographic and cryo-EM analyses delineate a composite pocket formed by the Skp2 leucine-rich-repeat groove and the phosphate-recognition site of Cks1; Cks1-centered open-closed motions further influence druggability. Using HTRF/TR-FRET and AlphaScreen biochemistry, alongside cell-based target-engagement readouts in some studies, three small-molecule classes have emerged that disrupt this PPI: 1,3-diphenyl-pyrazines and triazolo[1,5-a]pyrimidines (lead E35) with low-micromolar potency, and "Skp2E3LI" compounds with micromolar cellular activity.
View Article and Find Full Text PDFNeurotoxicology
September 2025
PERITOX Laboratory (UMR_I 01), UPJV/INERIS INERIS, MIV/TEAM, Verneuil-en-Halatte France University of Picardie Jules Verne, CURS, Amiens, France.
Health risks related to 900 MHz 2 G frequency exposure remain inconclusive under current regulatory standards. Research into potential long-term effects is ongoing, particularly as the use of mobile networks and wireless devices increases. This study investigates the effects of non-thermal exposure levels of mobile phone 900 MHz radiofrequency electromagnetic field (RF-EMF) on rodent neurodevelopment.
View Article and Find Full Text PDFInt J Biol Macromol
August 2025
Federal University of Pernambuco, Av. Prof. Moraes Rego, 1235 - Cidade Universitária, 50670-901 Recife, Pernambuco, Brazil; Federal Rural University of Pernambuco, Street Dom Manuel de Medeiros, s/n - Dois Irmãos, 52171-900 Recife, Pernambuco, Brazil. Electronic address:
The aim of this study was to develop and characterize nanoemulsions stabilized with microbial exopolysaccharide (EPS) (NE) and explore their performance in encapsulating β-carotene (βC-NE), in addition to evaluating their proliferative effects and uptake colorectal adenocarcinoma cells (Caco-2). βC-NE was obtained by ultrasonic homogenization followed by encapsulation of 0.1 % (w/v) β-carotene dispersed in the oil phase and was characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), proton nuclear magnetic resonance (H NMR), and observed by transmission electron microscopy (TEM) and scanning electron microscopy (SEM).
View Article and Find Full Text PDFFront Clin Diabetes Healthc
August 2025
Department of Endocrinology and Nutrition, University Hospital Virgen Macarena, Seville, Spain.
Aims: To analyze the impact of the COVID-19 pandemic on the activity and outcomes of the Andalusian Program for Early Detection of Diabetic Retinopathy (APDR).
Methods: A retrospective observational study was conducted during 2018-2023. The following variables were analyzed annually: newly included patients, retinal photographs performed, and pathological findings categorized by severity.
J Pharmacol Exp Ther
August 2025
Center for Molecular Medicine, MaineHealth Institute for Research, MaineHealth, Scarborough, Maine; Graduate School of Biomedical Science and Engineering, University of Maine, Orono, Maine. Electronic address:
Human highly proliferative cells (hHiPCs) isolated from the adult heart have progenitor and angiogenic properties. However, the mechanisms underlying hHiPCs in myocardial repair in vivo have yet to be investigated. We characterized the hHiPC proteome and secretome and found that hHiPCs express and secrete proangiogenic and proreparative proteins, including CXCL6, CTHRC1, and CD73, and are ontologically enriched in pathways related to cytokine signaling and glucose metabolism.
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