Ernst Sabrina, Müller-Newen Gerhard
Institute of Biochemistry and Molecular Biology, RWTH Aachen University, 52074 Aachen, Germany.
Confocal Microscopy Facility, Interdisciplinary Center for Clinical Research IZKF, RWTH Aachen University, 52074 Aachen, Germany.
Cancers (Basel). 2019 Nov 19;11(11):1815. doi: 10.3390/cancers11111815.
Signal transducer and activator of transcription (STAT) proteins are transcription factors that in the latent state are located predominantly in the cytoplasm. Activation of STATs through phosphorylation of a single tyrosine residue results in nuclear translocation. The requirement of tyrosine phosphorylation for nuclear accumulation is shared by all STAT family members but mechanisms of nuclear translocation vary between different STATs. These differences offer opportunities for specific intervention. To achieve this, the molecular mechanisms of nucleocytoplasmic shuttling of STATs need to be understood in more detail. In this review we will give an overview on the various aspects of nucleocytoplasmic shuttling of latent and activated STATs with a special focus on STAT3 and STAT5. Potential targets for cancer treatment will be identified and discussed.
信号转导及转录激活蛋白(STAT)是一类转录因子,在潜伏状态下主要位于细胞质中。通过单个酪氨酸残基的磷酸化激活STAT会导致其向细胞核转位。所有STAT家族成员都需要酪氨酸磷酸化才能进行核内积累,但不同STAT的核转位机制有所不同。这些差异为特异性干预提供了机会。要实现这一点,需要更详细地了解STAT在核质穿梭的分子机制。在这篇综述中,我们将概述潜伏和激活的STAT在核质穿梭的各个方面,特别关注STAT3和STAT5。我们还将确定并讨论癌症治疗的潜在靶点。