The Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Shantou University Medical College, Shantou 515041, Guangdong, PR China; Institute of Oncological Pathology, Shantou University Medical College, Shantou, Guangdong, PR China.
The Key Laboratory of Molecular Biology for High Cancer Incidence Coastal Chaoshan Area, Shantou University Medical College, Shantou 515041, Guangdong, PR China; Department of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou 515041, Guangdong, PR China.
Int J Biochem Cell Biol. 2019 May;110:130-139. doi: 10.1016/j.biocel.2019.02.006. Epub 2019 Feb 26.
STAT3β is an isoform of STAT3 (signal transducer and activator of transcription 3) that differs from the STAT3α isoform by the replacement of the C-terminal 55 amino acid residues with 7 specific residues. The constitutive activation of STAT3α plays a pivotal role in the activation of oncogenic pathways, such as cell proliferation, maturation and survival, while STAT3β is often referred to as a dominant-negative regulator of cancer. STAT3β reveals a "spongy cushion" effect through its cooperation with STAT3α or forms a ternary complex with other co-activators. Especially in tumour cells, relatively high levels of STAT3β lead to some favourable changes. However, there are still many mechanisms that have not been clearly explained in contrast to STAT3α, such as STAT3β nuclear retention, more stable heterodimers and the prolonged Y705 phosphorylation. In addition to its transcriptional activities, STAT3β may also function in the cytosol with respect to the mitochondria, cytoskeleton rearrangements and metastasis of cancer cells. In this review, we summarize the mechanisms that underlie the unique roles of STAT3β combined with total STAT3 to enlighten and draw the attention of researchers studying STAT3 and discuss some interesting questions that warrant answers.
STAT3β 是 STAT3(信号转导和转录激活因子 3)的一种异构体,与 STAT3α 异构体的区别在于 C 端的 55 个氨基酸残基被 7 个特定的残基取代。STAT3α 的组成性激活在致癌途径的激活中起着关键作用,如细胞增殖、成熟和存活,而 STAT3β 通常被称为癌症的显性负调控因子。STAT3β 通过与 STAT3α 合作或与其他共激活因子形成三元复合物,揭示出“海绵垫”效应。特别是在肿瘤细胞中,相对较高水平的 STAT3β 导致一些有利的变化。然而,与 STAT3α 相比,仍有许多机制尚未得到明确解释,如 STAT3β 核保留、更稳定的异二聚体和 Y705 磷酸化的延长。除了其转录活性外,STAT3β 可能在细胞质中也具有功能,涉及线粒体、细胞骨架重排和癌细胞的转移。在这篇综述中,我们总结了 STAT3β 与总 STAT3 结合的独特作用的机制,以启发和引起研究 STAT3 的研究人员的注意,并讨论了一些值得回答的有趣问题。