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Src Family Kinases as Therapeutic Targets in Advanced Solid Tumors: What We Have Learned So Far

机译:Src家族激酶作为晚期实体瘤的治疗靶点:到目前为止我们所学到的

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摘要

Src is the prototypal member of Src Family tyrosine Kinases (SFKs), a large non-receptor kinase class that controls multiple signaling pathways in animal cells. SFKs activation is necessary for the mitogenic signal from many growth factors, but also for the acquisition of migratory and invasive phenotype. Indeed, oncogenic activation of SFKs has been demonstrated to play an important role in solid cancers; promoting tumor growth and formation of distant metastases. Several drugs targeting SFKs have been developed and tested in preclinical models and many of them have successfully reached clinical use in hematologic cancers. Although in solid tumors SFKs inhibitors have consistently confirmed their ability in blocking cancer cell progression in several experimental models; their utilization in clinical trials has unveiled unexpected complications against an effective utilization in patients. In this review, we summarize basic molecular mechanisms involving SFKs in cancer spreading and metastasization; and discuss preclinical and clinical data highlighting the main challenges for their future application as therapeutic targets in solid cancer progression
机译:Src是Src家族酪氨酸激酶(SFK)的原型成员,SFK是控制动物细胞中多种信号通路的大型非受体激酶类。 SFK的激活对于来自许多生长因子的有丝分裂信号是必需的,而且对于迁移性和侵入性表型的获得也是必需的。确实,已证明SFK的致癌激活在实体癌中起重要作用。促进肿瘤生长和远处转移的形成。已经开发了几种针对SFK的药物并已在临床前模型中进行了测试,其中许多药物已成功地用于血液系统癌症的临床应用。尽管在实体瘤中,SFKs抑制剂已在几种实验模型中一致证实了其阻断癌细胞进程的能力;它们在临床试验中的利用揭示了意想不到的并发症,不利于患者有效利用。在这篇综述中,我们总结了涉及SFKs在癌症扩散和转移中的基本分子机制。并讨论临床前和临床数据,重点介绍将其作为实体癌症进展中的治疗靶标未来应用的主要挑战

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