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CENP-A Regulation and Cancer

Authors :
Charlène Renaud-Pageot
Jean-Pierre Quivy
Marina Lochhead
Geneviève Almouzni
Université Paris sciences et lettres (PSL)
Centre National de la Recherche Scientifique (CNRS)
Sorbonne Université (SU)
Dynamique du noyau [Institut Curie]
Institut Curie [Paris]-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Source :
Frontiers in Cell and Developmental Biology, Frontiers in Cell and Developmental Biology, Frontiers media, 2022, 10, ⟨10.3389/fcell.2022.907120⟩
Publication Year :
2022
Publisher :
HAL CCSD, 2022.

Abstract

International audience; In mammals, CENP-A, a histone H3 variant found in the centromeric chromatin, is critical for faithful chromosome segregation and genome integrity maintenance through cell divisions. Specifically, it has dual functions, enabling to define epigenetically the centromere position and providing the foundation for building up the kinetochore. Regulation of its dynamics of synthesis and deposition ensures to propagate proper centromeres on each chromosome across mitosis and meiosis. However, CENP-A overexpression is a feature identified in many cancers. Importantly, high levels of CENP-A lead to its mislocalization outside the centromere. Recent studies in mammals have begun to uncover how CENP-A overexpression can affect genome integrity, reprogram cell fate and impact 3D nuclear organization in cancer. Here, we summarize the mechanisms that orchestrate CENP-A regulation. Then we review how, beyond its centromeric function, CENP-A overexpression is linked to cancer state in mammalian cells, with a focus on the perturbations that ensue at the level of chromatin organization. Finally, we review the clinical interest for CENP-A in cancer treatment.

Details

Language :
English
ISSN :
2296634X
Database :
OpenAIRE
Journal :
Frontiers in Cell and Developmental Biology, Frontiers in Cell and Developmental Biology, Frontiers media, 2022, 10, ⟨10.3389/fcell.2022.907120⟩
Accession number :
edsair.doi.dedup.....7badd996b7172d3f55184002056edf42
Full Text :
https://doi.org/10.3389/fcell.2022.907120⟩