| Literature DB >> 26437781 |
Y Saitoh1, A Hamano1, K Mochida1, A Kakeya1, M Uno1,2, E Tsuruyama1, H Ichikawa1, F Tokunaga3, A Utsunomiya4, T Watanabe5, S Yamaoka1.
Abstract
Adult T-cell leukemia (ATL) arises from a human T-cell leukemia virus type I (HTLV-I)-infected cell and has few therapeutic options. Here, we have uncovered a previously unrecognized role for a ubiquitin-editing enzyme A20 in the survival of HTLV-I-infected cells. Unlike in lymphomas of the B-cell lineage, A20 is abundantly expressed in primary ATL cells without notable mutations. Depletion of A20 in HTLV-I-infected cells resulted in caspase activation, cell death induction and impaired tumorigenicity in mouse xenograft models. Mechanistically, A20 stably interacts with caspase-8 and Fas-associated via death domain (FADD) in HTLV-I-infected cells. Mutational studies revealed that A20 supports the growth of HTLV-I-infected cells independent of its catalytic functions and that the zinc-finger domains are required for the interaction with and regulation of caspases. These results indicate a pivotal role for A20 in the survival of HTLV-I-infected cells and implicate A20 as a potential therapeutic target in ATL.Entities:
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Year: 2015 PMID: 26437781 DOI: 10.1038/leu.2015.267
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528