Genetic mechanisms underlying tumor microenvironment composition and function in diffuse large B-cell lymphoma

被引:11
|
作者
Cerchietti, Leandro [1 ]
机构
[1] Cornell Univ, New York Presbyterian Hosp, Meyer Canc Ctr, Weill Cornell Med,Med Dept,Hematol & Oncol Div, 1300 York Ave, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
DLBCL cells; including mutations; somatic copy number alter; EXPRESSION; ATHEROSCLEROSIS; POLYMORPHISMS; INACTIVATION; REPRESSION; MYC;
D O I
10.1182/blood.2023021002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cells in the tumor microenvironment (TME) of diffuse large B-cell lymphoma (DLBCL) show enormous diversity and plasticity, with functions that can range from tumor inhibitory to tumor supportive. The patient's age, immune status, and DLBCL treatments are factors that contribute to the shaping of this TME, but evidence suggests that genetic factors, arising principally in lymphoma cells themselves, are among the most important. Here, we review the current understanding of the role of these genetic drivers of DLBCL in establishing and modulating the lymphoma microenvironment. A better comprehension of the relationship between lymphoma genetic factors and TME biology should lead to better therapeutic interventions, especially immunotherapies.
引用
收藏
页码:1101 / 1111
页数:11
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