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Mitotic catastrophe and endomitosis in tumour cells: An evolutionary key to a molecular solution

Mitotic catastrophe and endomitosis in tumour cells: An evolutionary key to a molecular solution
Mitotic catastrophe and endomitosis in tumour cells: An evolutionary key to a molecular solution
Following genotoxic insult, p53 mutated tumour cells undergo mitotic catastrophe. This is characterised by a switch from mitosis to the endocycle. The essential difference between mitosis and the endocycle is that in the latter, DNA synthesis is uncoupled from cell division, which leads to the formation of endopolyploid cells. Recent data suggests that a return from the endocycle into mitosis is also possible. Furthermore, our observations indicate that a particular type of endocycle known as endomitosis may be involved in this return. Here we review the role of endomitosis in the somatic reduction of polyploidy during development and its postulated role in the evolution of meiosis. Finally, we incorporate these evolutionary data to help interpret our most recent observations in the tumour cell system, which indicate a role for endomitosis and meiotic regulators, in particular p39mos in the segregation of genomes (somatic reduction) of these endopolyploid cells.
cancer, meiotic regulators, division, cells, kinase, mechanism, somatic reduction, transformation, development, endomitosis, mitotic catastrophe, dna, giant-cells, tumours, polyploidization, mos, p53, cell, aberrations, cycle, meiosis
1065-6995
1012-1018
Erenpreisa, J.
6bc35d80-54c7-432c-bf95-6e8bc2e70ecc
Kalejs, M.
da6c9cb7-b672-458b-b0fd-8e05d28cdd3c
Cragg, M. S.
ec97f80e-f3c8-49b7-a960-20dff648b78c
Erenpreisa, J.
6bc35d80-54c7-432c-bf95-6e8bc2e70ecc
Kalejs, M.
da6c9cb7-b672-458b-b0fd-8e05d28cdd3c
Cragg, M. S.
ec97f80e-f3c8-49b7-a960-20dff648b78c

Erenpreisa, J., Kalejs, M. and Cragg, M. S. (2005) Mitotic catastrophe and endomitosis in tumour cells: An evolutionary key to a molecular solution. Cell Biology International, 29 (12), 1012-1018. (doi:10.1016/j.cellbi.2005.10.005).

Record type: Article

Abstract

Following genotoxic insult, p53 mutated tumour cells undergo mitotic catastrophe. This is characterised by a switch from mitosis to the endocycle. The essential difference between mitosis and the endocycle is that in the latter, DNA synthesis is uncoupled from cell division, which leads to the formation of endopolyploid cells. Recent data suggests that a return from the endocycle into mitosis is also possible. Furthermore, our observations indicate that a particular type of endocycle known as endomitosis may be involved in this return. Here we review the role of endomitosis in the somatic reduction of polyploidy during development and its postulated role in the evolution of meiosis. Finally, we incorporate these evolutionary data to help interpret our most recent observations in the tumour cell system, which indicate a role for endomitosis and meiotic regulators, in particular p39mos in the segregation of genomes (somatic reduction) of these endopolyploid cells.

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More information

Published date: 2005
Keywords: cancer, meiotic regulators, division, cells, kinase, mechanism, somatic reduction, transformation, development, endomitosis, mitotic catastrophe, dna, giant-cells, tumours, polyploidization, mos, p53, cell, aberrations, cycle, meiosis

Identifiers

Local EPrints ID: 62734
URI: http://eprints.soton.ac.uk/id/eprint/62734
ISSN: 1065-6995
PURE UUID: 824c1bc5-0ab7-4df6-a9a0-12f9da349469
ORCID for M. S. Cragg: ORCID iD orcid.org/0000-0003-2077-089X

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Date deposited: 11 Sep 2008
Last modified: 16 Mar 2024 02:58

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Contributors

Author: J. Erenpreisa
Author: M. Kalejs
Author: M. S. Cragg ORCID iD

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