作者
Andrew C. Pearce,Mark J. Bamford,Ruth Barber,Angela Bridges,M.A. Convery,Constantinos Demetriou,Siân Evans,Thomas Gobbetti,David J. Hirst,Duncan S. Holmes,Jonathan P. Hutchinson,Sandrine Jayne,Larissa Lezina,Michael T. McCabe,Cassie Messenger,J Morley,Melissa C. Musso,Paul Scott‐Stevens,Ana Sousa Manso,Jennifer Schofield,Tom Slocombe,Don O. Somers,Ann L. Walker,Anastasia Wyce,Xiping Zhang,Simon D. Wagner
摘要
B-cell lymphoma 6 (BCL6) is a zinc finger transcriptional repressor possessing a BTB-POZ (BR-C, ttk, and bab for BTB; pox virus and zinc finger for POZ) domain, which is required for homodimerization and association with corepressors. BCL6 has multiple roles in normal immunity, autoimmunity, and some types of lymphoma. Mice bearing disrupted BCL6 loci demonstrate suppressed high-affinity antibody responses to T-dependent antigens. The corepressor binding groove in the BTB-POZ domain is a potential target for small compound-mediated therapy. Several inhibitors targeting this binding groove have been described, but these compounds have limited or absent in vivo activity. Biophysical studies of a novel compound, GSK137, showed an in vitro pIC