
Radiotherapy and Oncology, Год журнала: 2024, Номер 203, С. 110669 - 110669
Опубликована: Дек. 13, 2024
Язык: Английский
Radiotherapy and Oncology, Год журнала: 2024, Номер 203, С. 110669 - 110669
Опубликована: Дек. 13, 2024
Язык: Английский
Cancer Cell, Год журнала: 2024, Номер 42(11), С. 1825 - 1863
Опубликована: Окт. 10, 2024
Язык: Английский
Процитировано
70Nature reviews. Immunology, Год журнала: 2025, Номер unknown
Опубликована: Янв. 7, 2025
Язык: Английский
Процитировано
5The EMBO Journal, Год журнала: 2025, Номер unknown
Опубликована: Фев. 21, 2025
The cGAS-STING signalling pathway has a central role in the innate immune response to extrinsic and intrinsic sources of cytoplasmic dsDNA. At core this is cGAS-dependent production intra- extra-cellular messenger cGAMP, which activates STING leads IRF3-dependent expression cytokines interferons. Despite its relevance viral bacterial infections, cell death, genome instability, lack specific live-cell reporters precluded spatiotemporal analyses signalling. Here, we generate fluorescent biosensor termed SIRF (STING-IRF3), reports on functional interaction between activated IRF3 at Golgi. We show that cells harbouring react time- concentration-dependent manner both agonists microenvironmental cGAMP. demonstrate new suitable for single-cell characterisation responses HSV-1 infection, mtDNA release upon apoptosis, or other Furthermore, our results indicate not by ruptured micronuclei, suggesting cytosolic pattern recognition receptors underlie interferon chromosomal instability.
Язык: Английский
Процитировано
1Nature Reviews Molecular Cell Biology, Год журнала: 2025, Номер unknown
Опубликована: Март 17, 2025
Язык: Английский
Процитировано
1Nature Cell Biology, Год журнала: 2025, Номер 27(1), С. 7 - 8
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0International Journal of Radiation Oncology*Biology*Physics, Год журнала: 2025, Номер 121(2), С. 283 - 286
Опубликована: Янв. 15, 2025
Язык: Английский
Процитировано
0Biology Open, Год журнала: 2025, Номер 14(1)
Опубликована: Янв. 15, 2025
ABSTRACT Chromosomal aneuploidies are a major cause of developmental failure and pregnancy loss. To investigate the possible consequences aneuploidy on early embryonic development in vitro, we focused primed pluripotent stem cells that relatable to epiblast post-implantation embryos vivo. We used human induced (iPSCs) as an model altered chromosome numbers by treating with reversine, small-molecule inhibitor monopolar spindle 1 kinase (MSP1) inactivates assembly checkpoint, which has been strongly implicated mis-segregation generation. Upon reversine treatment, obtained varied chromosomal content retained pluripotency potential differentiate into three germ lineages. However, these displayed lagging chromosomes, increased micronuclei content, high p53 expression excessive apoptotic activity. Cell proliferation was not affected. Prolonged vitro culture resulted selective pool supernumerary exhibited cellular hypertrophy, enlarged nuclei, overproduction total RNAs proteins. conclude DNA damage responses, apoptosis, improper mass functions mechanisms contribute abnormal development.
Язык: Английский
Процитировано
0Chinese Chemical Letters, Год журнала: 2025, Номер unknown, С. 110990 - 110990
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Biology of the Cell, Год журнала: 2025, Номер 117(2)
Опубликована: Фев. 1, 2025
ABSTRACT Background Information Mitosis is crucial for the faithful transmission of genetic material, and disruptions can result in chromosomal instability (CIN), a hallmark cancer. CIN known driver tumor heterogeneity anti‐cancer drug resistance, thus highlighting need to assess levels cancer cells design effective targeted therapy. While micronuclei are widely recognized as markers, we have recently identified toroidal nucleus, novel ring‐shaped nuclear phenotype arising well from chromosome mis‐segregation. Results Here, examined whether increasing envelope stiffness through lamin A/C overexpression could affect formation nuclei micronuclei. Interestingly, led an increase while reducing prevalence. We demonstrated that chromatin compaction drive nuclei. Furthermore, inhibition autophagy lysosomal function elevated frequency without affecting number whole cell population. this divergence between two biomarkers independent defects A processing. Conclusions Significance These findings uncover complex interplay architecture CIN, advancing our understanding mechanisms supporting genomic stability further contributing biology.
Язык: Английский
Процитировано
0Cancer Discovery, Год журнала: 2025, Номер 15(3), С. 461 - 480
Опубликована: Март 3, 2025
Abstract Thirty years ago, the cloning of first breast cancer susceptibility gene, BRCA1, marked a milestone in our understanding hereditary and ovarian cancers. This discovery initiated extensive research into DNA repair mechanisms, BRCA1-associated tumorigenesis, therapeutic interventions. Despite these advances, critical questions remain unanswered, such as evolution tumors their tissue specificity. These issues hinder development effective treatment prevention strategies, which ultimately aim to improve quality life for BRCA1 mutation carriers. In this review, we discuss current knowledge, identify existing gaps, suggest possible avenues tackle challenges. Significance: Here, explore impact three decades on lives carriers propose strategies cancer.
Язык: Английский
Процитировано
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