共 245 条
Targeting the Bcl-2 Family in B Cell Lymphoma
被引:123
作者:

Adams, Clare M.
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Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Canc Biol, Philadelphia, PA 19107 USA Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Canc Biol, Philadelphia, PA 19107 USA

Clark-Garvey, Sean
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Thomas Jefferson Univ, Sidney Kimmel Med Coll, Dept Internal Med, Internal Med Residency Program, Philadelphia, PA 19107 USA Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Canc Biol, Philadelphia, PA 19107 USA

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Eischen, Christine M.
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机构:
Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Canc Biol, Philadelphia, PA 19107 USA Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Dept Canc Biol, Philadelphia, PA 19107 USA
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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