Can one target T-cell ALL?

Can one target T-cell ALL?
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DOI:
10.1016/j.beha.2018.10.001
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发表时间:
2018-12
期刊:
Best practice & research. Clinical haematology
影响因子:
--
通讯作者:
Ferrando A
Ferrando A
中科院分区:
其他
文献类型:
--
作者:
Ferrando A

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我们对T细胞急性淋巴细胞白血病(T-ALL)病理生物学中的中心基因、途径和机制的理解取得了进展,已经确定了该疾病的关键驱动因素,为治疗开辟了新的机会。正在探索针对NOTCH 1和CDKN 2A中高度流行的遗传改变的药物,并且正在研究具有现成治疗剂和免疫疗法的多种其他靶标。本文就T-ALL的分子基础、潜在靶点和治疗靶点进行综述。
Progress in our understanding of the central genes, pathways, and mechanisms in the pathobiology of T-cell acute lymphoblastic leukemia (T-ALL) has identified key drivers of the disease, opening new opportunities for therapy. Drugs targeting highly prevalent genetic alterations in NOTCH1 and CDKN2A are being explored, and multiple other targets with readily available therapeutic agents, and immunotherapies are being investigated. The molecular basis of T-ALL is reviewed here and potential targets and therapeutic targets discussed.
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