Wagner Kay-Uwe, Schmidt Jeffrey W
Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, 985950 Nebraska Medical Center, DRC2, Rm. 5033, Omaha, NE, USA.
J Carcinog. 2011;10:32. doi: 10.4103/1477-3163.90677. Epub 2011 Dec 8.
Since its discovery as "just another kinase" more than twenty years ago, the family of JAK tyrosine kinases and their respective Signal Transducers and Activators of Transcription (STATs) has been a center of attention in the areas of signal transduction, development, and cancer. The subsequent designation of JAKs as Janus kinases after the mythical two-faced Roman God of the doorways accurately portrays the analogous and sometimes contrasting molecular and biological characteristics of these tyrosine kinases. The two "faces" of JAKs are their structurally similar kinase and pseudo-kinase domains. As essential parts of various transmembrane receptor complexes, these tyrosine kinases function at cellular gateways and relay signals from growth factors to their respective intracellular targets. The multifaceted nature of JAKs becomes evident from their ability to activate specific STATs during distinct phases of normal mammary gland development. Studies in breast cancer cells and genetically engineered mouse models also show that JAK/STAT signaling possesses a "two-faced" role during breast cancer initiation and progression. This review will highlight recent findings about important biological functions of JAKs and STATs during normal mammogenesis, with particular emphasis on the Jak2/Stat5 pathway as well as Jak1/2/Stat3 signaling complexes. In addition, we will discuss how the importance of these signaling networks changes during carcinogenesis. With JAK inhibitors currently under development to treat myeloproliferative disorders, determining the essential functions of JAKs at particular stages of disease initiation and progression is of critical importance to predict the efficacy of these agents for targeted therapies against breast cancer.
二十多年前,JAK酪氨酸激酶家族及其各自的信号转导和转录激活因子(STATs)被发现时还只是“另一种激酶”,此后它们一直是信号转导、发育和癌症领域的关注焦点。继JAKs之后,以罗马神话中掌管门道的两面神雅努斯命名为Janus激酶,这准确地描绘了这些酪氨酸激酶类似但有时又相互矛盾的分子和生物学特征。JAKs的两个“面”是其结构相似的激酶结构域和假激酶结构域。作为各种跨膜受体复合物的重要组成部分,这些酪氨酸激酶在细胞的“门道”处发挥作用,将生长因子的信号传递给各自的细胞内靶点。JAKs的多面性从其在正常乳腺发育的不同阶段激活特定STATs的能力中可见一斑。对乳腺癌细胞和基因工程小鼠模型的研究也表明,JAK/STAT信号在乳腺癌的发生和发展过程中具有“两面性”作用。本综述将重点介绍JAKs和STATs在正常乳腺发生过程中重要生物学功能的最新研究发现,特别强调Jak2/Stat5途径以及Jak1/2/Stat3信号复合物。此外,我们还将讨论这些信号网络在致癌过程中的重要性是如何变化的。鉴于目前正在开发用于治疗骨髓增殖性疾病的JAK抑制剂,确定JAKs在疾病发生和发展的特定阶段的基本功能对于预测这些药物针对乳腺癌的靶向治疗效果至关重要。