MALT1 small molecule inhibitors specifically suppress ABC-DLBCL in vitro and in vivo.

نویسندگان

  • Lorena Fontan
  • Chenghua Yang
  • Venkataraman Kabaleeswaran
  • Laurent Volpon
  • Michael J Osborne
  • Elena Beltran
  • Monica Garcia
  • Leandro Cerchietti
  • Rita Shaknovich
  • Shao Ning Yang
  • Fang Fang
  • Randy D Gascoyne
  • Jose Angel Martinez-Climent
  • J Fraser Glickman
  • Katherine Borden
  • Hao Wu
  • Ari Melnick
چکیده

MALT1 cleavage activity is linked to the pathogenesis of activated B cell-like diffuse large B cell lymphoma (ABC-DLBCL), a chemoresistant form of DLBCL. We developed a MALT1 activity assay and identified chemically diverse MALT1 inhibitors. A selected lead compound, MI-2, featured direct binding to MALT1 and suppression of its protease function. MI-2 concentrated within human ABC-DLBCL cells and irreversibly inhibited cleavage of MALT1 substrates. This was accompanied by NF-κB reporter activity suppression, c-REL nuclear localization inhibition, and NF-κB target gene downregulation. Most notably, MI-2 was nontoxic to mice, and displayed selective activity against ABC-DLBCL cell lines in vitro and xenotransplanted ABC-DLBCL tumors in vivo. The compound was also effective against primary human non-germinal center B cell-like DLBCLs ex vivo.

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عنوان ژورنال:
  • Cancer cell

دوره 22 6  شماره 

صفحات  -

تاریخ انتشار 2012