Drennan Amanda C, Rui Lixin
a Department of Medicine and Carbone Cancer Center , University of Wisconsin School of Medicine and Public Health , Madison , WI , USA.
Leuk Lymphoma. 2017 Nov;58(11):2540-2547. doi: 10.1080/10428194.2017.1312370. Epub 2017 Apr 12.
The Janus kinase (JAK)/signal transducer and activator of transcription (STAT) pathway is central to signaling by receptors of diverse cytokines, growth factors, and other related molecules. Many of these receptors transmit anti-apoptosis, proliferation, and differentiation signals that are critical for normal hematopoiesis and immune response. However, the JAK/STAT signaling pathway is deregulated in many hematologic malignancies, and as such is co-opted by malignant cells to promote their survival and proliferation. It has recently come to light that an alternative mechanism, wherein nuclear JAKs epigenetically modify the chromatin to increase gene expression independent of STATs, also plays an important role in the pathogenesis of many hematologic malignancies. In this review, we will focus on common genetic alterations of the JAK family members in leukemia and lymphoma, and provide examples in which JAKs regulate gene expression by targeting the cancer epigenome.
Janus激酶(JAK)/信号转导子和转录激活子(STAT)通路对于多种细胞因子、生长因子及其他相关分子的受体信号传导至关重要。这些受体中的许多传递抗凋亡、增殖和分化信号,这些信号对于正常造血和免疫反应至关重要。然而,JAK/STAT信号通路在许多血液系统恶性肿瘤中失调,因此被恶性细胞利用以促进其存活和增殖。最近发现,一种替代机制,即核JAK通过表观遗传修饰染色质以独立于STAT增加基因表达,在许多血液系统恶性肿瘤的发病机制中也起重要作用。在本综述中,我们将重点关注白血病和淋巴瘤中JAK家族成员的常见基因改变,并提供JAK通过靶向癌症表观基因组调节基因表达的实例。