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Boveri and beyond: Chromothripsis and genomic instability from mitotic errors.
Mazzagatti, Alice; Engel, Justin L; Ly, Peter.
Afiliación
  • Mazzagatti A; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Engel JL; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Ly P; Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA; Department of Cell Biology, Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA. Electronic address: peter.ly@utsouthwestern.edu.
Mol Cell ; 84(1): 55-69, 2024 Jan 04.
Article en En | MEDLINE | ID: mdl-38029753
ABSTRACT
Mitotic cell division is tightly monitored by checkpoints that safeguard the genome from instability. Failures in accurate chromosome segregation during mitosis can cause numerical aneuploidy, which was hypothesized by Theodor Boveri over a century ago to promote tumorigenesis. Recent interrogation of pan-cancer genomes has identified unexpected classes of chromosomal abnormalities, including complex rearrangements arising through chromothripsis. This process is driven by mitotic errors that generate abnormal nuclear structures that provoke extensive yet localized shattering of mis-segregated chromosomes. Here, we discuss emerging mechanisms underlying chromothripsis from micronuclei and chromatin bridges, as well as highlight how this mutational cascade converges on the DNA damage response. A fundamental understanding of these catastrophic processes will provide insight into how initial errors in mitosis can precipitate rapid cancer genome evolution.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Cromotripsis / Neoplasias Límite: Humans Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Cromotripsis / Neoplasias Límite: Humans Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos