Department of Microbiology, Immunology, and Genetics, University of North Texas Health Science Center, 3500 Camp Bowie Blvd, Fort Worth, TX, 76107, USA.
MTA TTK Lendület Cancer Biomarker Research Group, Institute of Enzymology, Magyar Tudósok körútja 2, Budapest, 1117, Hungary.
Mol Cancer. 2018 Aug 17;17(1):124. doi: 10.1186/s12943-018-0868-z.
Tip110, an important regulator of several oncogenic proteins, was significantly downregulated in human metastatic melanoma cells exposed to a hypoxic condition. Therefore, in this study, we set to determine whether differential expression of Tip110 could be an important indicator for melanoma tumorigenesis and metastasis. We found that in melanoma, but not in other cancer types, Tip110 knockdown enhanced significant expression and secretion of IL-8 and melanoma cells invasions. This induction was further potentiated under hypoxia and by inflammatory cytokine and found independent of TNF-α autocrine signaling. We further showed that Tip110 knockdown-mediated IL-8 induction involved IL-8 mRNA stability. Furthermore, the transcriptomic profiling data and survival from 455 melanoma patients demonstrated that the correlation between Tip110 expression and the clinical outcomes in melanoma was stage-dependent. These findings uncover important roles of Tip110 in melanoma tumorigenesis and metastasis through regulation of IL-8 and hope to provide new clues for future therapeutic strategies.
Tip110 是几种致癌蛋白的重要调节因子,在暴露于缺氧条件下的人类转移性黑色素瘤细胞中表达显著下调。因此,在本研究中,我们旨在确定 Tip110 的差异表达是否可以作为黑色素瘤发生和转移的重要指标。我们发现,在黑色素瘤中,而不是在其他癌症类型中,Tip110 的敲低增强了 IL-8 的显著表达和分泌以及黑色素瘤细胞的侵袭。在缺氧和炎症细胞因子的作用下,这种诱导作用进一步增强,且不依赖于 TNF-α 自分泌信号。我们进一步表明,Tip110 敲低介导的 IL-8 诱导涉及 IL-8 mRNA 稳定性。此外,455 名黑色素瘤患者的转录组谱数据和生存分析表明,Tip110 表达与黑色素瘤临床结局的相关性依赖于疾病分期。这些发现揭示了 Tip110 通过调节 IL-8 在黑色素瘤发生和转移中的重要作用,并有望为未来的治疗策略提供新的线索。