| Literature DB >> 30804013 |
Stéphanie Torrino1, François-René Roustan1, Lisa Kaminski1, Thomas Bertero2, Sabrina Pisano2, Damien Ambrosetti3, Maeva Dufies2, Jay P Uhler4, Emmanuel Lemichez5, Amel Mettouchi5, Maeva Gesson1, Kathiane Laurent1, Cedric Gaggioli2, Jean-Francois Michiels3, Christophe Lamaze6, Frédéric Bost7, Stéphan Clavel7.
Abstract
Ubiquitin domain-containing protein 1 (UBTD1) is highly evolutionary conserved and has been described to interact with E2 enzymes of the ubiquitin-proteasome system. However, its biological role and the functional significance of this interaction remain largely unknown. Here, we demonstrate that depletion of UBTD1 drastically affects the mechanical properties of epithelial cancer cells via RhoA activation and strongly promotes their aggressiveness. On a stiff matrix, UBTD1 expression is regulated by cell-cell contacts, and the protein is associated with β-catenin at cell junctions. Yes-associated protein (YAP) is a major cell mechano-transducer, and we show that UBTD1 is associated with components of the YAP degradation complex. Interestingly, UBTD1 promotes the interaction of YAP with its E3 ubiquitin ligase β-TrCP Consequently, in cancer cells, UBTD1 depletion decreases YAP ubiquitylation and triggers robust ROCK2-dependent YAP activation and downstream signaling. Data from lung and prostate cancer patients further corroborate the in cellulo results, confirming that low levels of UBTD1 are associated with poor patient survival, suggesting that biological functions of UBTD1 could be beneficial in limiting cancer progression.Entities:
Keywords: zzm321990YAPzzm321990; ROCK2; UBTD1; matrix stiffness; β‐TrCP
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Year: 2019 PMID: 30804013 PMCID: PMC6446246 DOI: 10.15252/embr.201846570
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807