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Springer Nature [academic journals on nature.com], Cell Death & Differentiation, 3(14), p. 411-421, 2006

DOI: 10.1038/sj.cdd.4402022

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Hypoxia induces p53-dependent transactivation and Fas/CD95-dependent apoptosis

Journal article published in 2006 by T. Liu, C. Laurell, G. Selivanova, J. Lundeberg, P. Nilsson ORCID, K. G. Wiman
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

p53 triggers apoptosis in response to cellular stress. We analyzed p53-dependent gene and protein expression in response to hypoxia using wild-type p53-carrying or p53 null HCT116 colon carcinoma cells. Hypoxia induced p53 protein levels and p53-dependent apoptosis in these cells. cDNA microarray analysis revealed that only a limited number of genes were regulated by p53 upon hypoxia. Most classical p53 target genes were not upregulated. However, we found that Fas/CD95 was significantly induced in response to hypoxia in a p53-dependent manner, along with several novel p53 target genes including ANXA1, DDIT3/GADD153 (CHOP), SEL1L and SMURF1. Disruption of Fas/CD95 signalling using anti-Fas-blocking antibody or a caspase 8 inhibitor abrogated p53-induced apoptosis in response to hypoxia. We conclude that hypoxia triggers a p53-dependent gene expression pattern distinct from that induced by other stress agents and that Fas/CD95 is a critical regulator of p53-dependent apoptosis upon hypoxia.