FBXO11 targets BCL6 for degradation and is inactivated in diffuse large B-cell lymphomas
Shanshan Duan,
Lukas Cermak,
Julia K. Pagan,
Mario Rossi,
Cinzia Martinengo,
Paola Francia di Celle,
Bjoern Chapuy,
Margaret Shipp,
Roberto Chiarle () and
Michele Pagano ()
Additional contact information
Shanshan Duan: NYU Cancer Institute, New York University School of Medicine, 522 First Avenue, SRB 1107, New York, New York 10016, USA
Lukas Cermak: NYU Cancer Institute, New York University School of Medicine, 522 First Avenue, SRB 1107, New York, New York 10016, USA
Julia K. Pagan: NYU Cancer Institute, New York University School of Medicine, 522 First Avenue, SRB 1107, New York, New York 10016, USA
Mario Rossi: NYU Cancer Institute, New York University School of Medicine, 522 First Avenue, SRB 1107, New York, New York 10016, USA
Cinzia Martinengo: CERMS, University of Torino, 10126 Torino, Italy
Paola Francia di Celle: San Giovanni Battista Hospital, Via Santena 7, 10126 Torino, Italy
Bjoern Chapuy: Medical Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115, USA
Margaret Shipp: Medical Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115, USA
Roberto Chiarle: CERMS, University of Torino, 10126 Torino, Italy
Michele Pagano: NYU Cancer Institute, New York University School of Medicine, 522 First Avenue, SRB 1107, New York, New York 10016, USA
Nature, 2012, vol. 481, issue 7379, 90-93
Abstract:
FBXO11 is identified as the F-box protein that normally targets BCL6 for degradation, and FBXO11 deletions or mutations that prevent this function and thus stabilize BCL6 are found in B-cell lymphomas.
Date: 2012
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Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:481:y:2012:i:7379:d:10.1038_nature10688
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DOI: 10.1038/nature10688
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