共 50 条
T-Cell Receptor Signaling in Peripheral T-Cell Lymphoma – A Review of Patterns of Alterations in a Central Growth Regulatory Pathway
被引:0
|作者:
Kathrin Warner
Nicole Weit
Giuliano Crispatzu
Joan Admirand
Dan Jones
Marco Herling
机构:
[1] University of Cologne,Laboratory for Lymphocyte Signaling and Oncoproteome, Department I of Internal Medicine, Center for Integrated Oncology Köln
[2] Clinical Pathology Associates,Bonn, and Cologne Cluster of Excellence in Cellular Stress Responses in Aging
[3] The University of Texas M.D. Anderson Cancer Center,associated Diseases (CECAD)
[4] University Hospital Cologne,School of Health Professions
来源:
Current Hematologic Malignancy Reports
|
2013年
/
8卷
关键词:
T-cell receptor (TCR);
Mature T-cell lymphoma/leukemia;
Peripheral T-cell lymphoma (PTCL);
Anaplastic large cell lymphoma (ALCL);
T-cell prolymphocytic leukemia (T-PLL);
T-cell homeostasis;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
T-cell receptor (TCR) signaling is pivotal in T-cell development and function. In peripheral T-cell lymphomas/leukemias (PTCL/L), histogenesis, transforming events, epidemiology, and clinical presentation are also closely linked to TCR-mediated influences. After reviewing the physiology of normal TCR signaling and cellular responses, we describe here the association of subgroups of PTCL/L with specific patterns of TCR activation as relevant tumor-initiating and/or tumor-sustaining programs. We identify PTCL/L with a functionally intact TCR machinery in which stimulation is possibly incited by exogenous antigens or autoantigens. Distinct from these are tumors with autonomous oncogenic signaling by dysregulated TCR components uncoupled from extrinsic receptor input. A further subset is characterized by transforming events that activate molecules acting as substitutes for TCR signaling, but triggering similar downstream cascades. We finally discuss the consequences of such a functional model for TCR-targeted therapeutic strategies including those that are being tested in the clinic and those that still require further development.
引用
收藏
页码:163 / 172
页数:9
相关论文