Δ133p53β isoform pro-invasive activity is regulated through an aggregation-dependent mechanism in cancer cells

p53 isoform Δ133p53β is reported to promote intrinsic oncogenic functions. Here the authors show Δ133p53β is sequestered as aggregates in an inactive form, while association with interacting partners including p63 isoforms and the CCT chaperone complex promotes Δ133p53β activity, resulting in enhanc...

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Main Authors: Nikola Arsic, Tania Slatter, Gilles Gadea, Etienne Villain, Aurelie Fournet, Marina Kazantseva, Frédéric Allemand, Nathalie Sibille, Martial Seveno, Sylvain de Rossi, Sunali Mehta, Serge Urbach, Jean-Christophe Bourdon, Pau Bernado, Andrey V. Kajava, Antony Braithwaite, Pierre Roux
Format: article
Language:EN
Published: Nature Portfolio 2021
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Online Access:https://doaj.org/article/68225466d9dc4ec1bb5844837f0a0ec8
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