Targeting the Bcl-2 Family in B Cell Lymphoma

被引:123
作者
Adams, Clare M. [1 ]
Clark-Garvey, Sean [2 ]
Porcu, Pierluigi [3 ]
Eischen, Christine M. [1 ]
机构
[1] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Canc Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Dept Internal Med, Internal Med Residency Program, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Med Oncol, Div Hematol Malignancies & Hematopoiet Stem Cell, Philadelphia, PA 19107 USA
关键词
BCL-2; BCL-W; B cell lymphoma; apoptosis; venetoclax; navitoclax; BH-3; mimetic; CLL; CHRONIC LYMPHOCYTIC-LEUKEMIA; RITUXIMAB PLUS CYCLOPHOSPHAMIDE; MYC-DRIVEN LYMPHOMAGENESIS; SMALL-MOLECULE INHIBITOR; STRUCTURE-GUIDED DESIGN; ACUTE MYELOID-LEUKEMIA; PHASE-I; X-L; BH3-ONLY PROTEINS; TRANSGENIC MICE;
D O I
10.3389/fonc.2018.00636
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although lymphoma is a very heterogeneous group of biologically complex malignancies, tumor cells across all B cell lymphoma subtypes share a set of underlying traits that promote the development and sustain malignant B cells. One of these traits, the ability to evade apoptosis, is essential for lymphoma development. Alterations in the Bcl-2 family of proteins, the key regulators of apoptosis, is a hallmark of B cell lymphoma. Significant efforts have been made over the last 30 years to advance knowledge of the biology, molecular mechanisms, and therapeutic potential of targeting Bcl-2 family members. In this review, we will highlight the complexities of the Bcl-2 family, including our recent discovery of overexpression of the anti-apoptotic Bcl-2 family member Bcl-w in lymphomas, and describe recent advances in the field that include the development of inhibitors of anti-apoptotic Bcl-2 family members for the treatment of B cell lymphomas and their performance in clinical trials.
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页数:21
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