Beyond TCR Signaling: Emerging Functions of Lck in Cancer and Immunotherapy

被引:126
作者
Bommhardt, Ursula [1 ]
Schraven, Burkhart [1 ]
Simeoni, Luca [1 ]
机构
[1] Otto Von Guericke Univ, Inst Mol & Clin Immunol, Leipziger Str 44, D-39120 Magdeburg, Germany
关键词
Lck; T cell; CAR; cancer; leukemia; brain; CHRONIC LYMPHOCYTIC-LEUKEMIA; B-CELL-RECEPTOR; PROTEIN-TYROSINE KINASE; CHRONIC MYELOID-LEUKEMIA; SRC FAMILY KINASES; N-TERMINAL REGION; T-CELLS; BCR-ABL; CD28; COSTIMULATION; THERAPEUTIC TARGET;
D O I
10.3390/ijms20143500
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
In recent years, the lymphocyte-specific protein tyrosine kinase (Lck) has emerged as one of the key molecules regulating T-cell functions. Studies using Lck knock-out mice or Lck-deficient T-cell lines have shown that Lck regulates the initiation of TCR signaling, T-cell development, and T-cell homeostasis. Because of the crucial role of Lck in T-cell responses, strategies have been employed to redirect Lck activity to improve the efficacy of chimeric antigen receptors (CARs) and to potentiate T-cell responses in cancer immunotherapy. In addition to the well-studied role of Lck in T cells, evidence has been accumulated suggesting that Lck is also expressed in the brain and in tumor cells, where it actively takes part in signaling processes regulating cellular functions like proliferation, survival and memory. Therefore, Lck has emerged as a novel druggable target molecule for the treatment of cancer and neuronal diseases. In this review, we will focus on these new functions of Lck.
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页数:18
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