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Mamm Genome. 2018 Dec;29(11-12):831-842. doi: 10.1007/s00335-018-9758-3. Epub 2018 Jul 10.

A mouse model of the Δ133p53 isoform: roles in cancer progression and inflammation.

Author information

1
Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
2
Maurice Wilkins Centre for Molecular Biodiscovery, University of Otago, Dunedin, New Zealand.
3
Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand. antony.braithwaite@otago.ac.nz.
4
Maurice Wilkins Centre for Molecular Biodiscovery, University of Otago, Dunedin, New Zealand. antony.braithwaite@otago.ac.nz.

Abstract

This review paper outlines studies on the Δ122p53 mouse, a model of the human Δ133p53 isoform, together with studies in other model organisms, cell culture, and where available, clinical investigations. In general, these studies imply that, in contrast to the canonical p53 tumor suppressor, Δ133p53 family members have oncogenic capability. Δ122p53 is multi-functional, conferring survival and proliferative advantages on cells, promoting invasion, metastasis and vascularization, as does Δ133p53. Cancers with high levels of Δ133p53 often have poor prognosis. Δ122p53 mediates its effects through the JAK-STAT and RhoA-ROCK signaling pathways. We propose that Δ133p53 isoforms have evolved as inflammatory signaling molecules to deal with the consequent tissue damage of p53 activation. However, if sustained expression of the isoforms occur, pathologies may result.

PMID:
29992419
DOI:
10.1007/s00335-018-9758-3
[Indexed for MEDLINE]

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