Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Portugal.
Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Portugal; Instituto de Histologia e Biologia do Desenvolvimento, Faculdade de Medicina, Universidade de Lisboa, Portugal.
Cell Signal. 2017 Oct;38:10-25. doi: 10.1016/j.cellsig.2017.06.011. Epub 2017 Jun 21.
T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological cancer that arises from clonal expansion of transformed T-cell precursors. In this review we summarize the current knowledge on the external stimuli and cell-intrinsic lesions that drive aberrant activation of pivotal, pro-tumoral intracellular signaling pathways in T-cell precursors, driving transformation, leukemia expansion, spread or resistance to therapy. In addition to their pathophysiological relevance, receptors and kinases involved in signal transduction are often attractive candidates for targeted drug development. As such, we discuss also the potential of T-ALL signaling players as targets for therapeutic intervention.
T 细胞急性淋巴细胞白血病(T-ALL)是一种侵袭性血液系统恶性肿瘤,起源于转化 T 细胞前体的克隆性扩增。在这篇综述中,我们总结了目前关于驱动 T 细胞前体中关键的、促肿瘤细胞内信号通路异常激活的外部刺激和细胞内损伤的知识,这些信号通路驱动转化、白血病扩增、扩散或对治疗的耐药性。除了它们的病理生理学相关性外,参与信号转导的受体和激酶通常是靶向药物开发的有吸引力的候选物。因此,我们还讨论了 T-ALL 信号转导因子作为治疗干预靶点的潜力。