| Literature DB >> 22388102 |
Mi-Ae Lyu1, Lawrence H Cheung, Walter N Hittelman, Yuying Liu, John W Marks, Min-Jeong Cho, Michael G Rosenblum.
Abstract
We generated a fusion protein Bax(345)/BLyS containing the truncated form of Bax (Bax(345)) at the N-terminus followed by a 218 linker to the B lymphocyte stimulator (BLyS). Bax(345)/BLyS was cytotoxic to a panel of diffuse large B cell lymphoma and mantle cell lymphoma lines expressing the BLyS receptors. Specific delivery of Bax(345)/BLyS to malignant B cells drove cells into apoptosis by mitochondrial dysfunction and treatment of cells with Bax(345)/BLyS induced down-regulation of Mcl-1, X-IAP, and survivin. Bax(345)/BLyS represents a new class of targeted therapeutic agents with a unique mechanism of action and may have therapeutic potential for malignant B cells.Entities:
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Year: 2012 PMID: 22388102 DOI: 10.1016/j.canlet.2012.02.029
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679