Signal transducer and activator of transcription 5 (STAT5), a crucial regulator of immune and cancer cells.

Ilka Wittig, Bernd Groner
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引用次数: 35

Abstract

STAT5 belongs to a small family of transcription factors with dual functions. The seven signal transducers and activators of transcription (STAT) act as signaling components between the plasma membrane and the nucleus, and as transcription factors with specific DNA binding ability in the nucleus. STAT5 regulates the expression of genes, which determine important cellular phenotypes. It can promote proliferation and inhibit apoptosis, but is also involved in the regulation of differentiation between specific gene expression. STAT5 can also contribute to the transformed phenotype. In many leukemias and some solid tumors, STAT5 is constitutively activated through receptors or receptor associated tyrosine kinases and contributes to the survival and the proliferation of malignant cells. STAT5 activity appears to be limiting for these phenotypes. Inhibition of STAT5 in these tumor cells results in growth arrest and apoptosis. Targeting of STATs and other downstream mediators of oncogenic tyrosine kinases provides a promising strategy for tumor therapy, which might be refractory to resistance mechanisms incapacitating tyrosine kinase inhibitors. The well-studied steps in the activation of STAT5 and its roles in different subcellular compartments suggest original interference strategies, which could be used to inhibit its function. The challenge for drug developers will be the exploitation of defined protein-protein or protein-DNA interactions as targets of inhibition.

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信号转导和转录激活因子5 (STAT5),免疫细胞和癌细胞的重要调节因子。
STAT5属于一个具有双重功能的转录因子小家族。7种信号转导和转录激活因子(STAT)作为质膜和细胞核之间的信号元件,是细胞核内具有特异性DNA结合能力的转录因子。STAT5调节决定重要细胞表型的基因的表达。它可以促进细胞增殖和抑制细胞凋亡,但也参与调控特定基因表达之间的分化。STAT5也有助于转化表型。在许多白血病和一些实体肿瘤中,STAT5通过受体或受体相关酪氨酸激酶组成性激活,并有助于恶性细胞的存活和增殖。STAT5活性似乎对这些表型有限制。抑制这些肿瘤细胞中的STAT5导致生长停滞和凋亡。靶向STATs和其他下游致癌酪氨酸激酶介质为肿瘤治疗提供了一种很有前途的策略,这可能是无法使酪氨酸激酶抑制剂失能的耐药机制。STAT5的激活步骤及其在不同亚细胞区室中的作用得到了充分的研究,这表明了原始的干扰策略,可以用来抑制其功能。药物开发人员面临的挑战将是利用确定的蛋白质-蛋白质或蛋白质- dna相互作用作为抑制靶点。
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