Department of Oncology, The Fifth People's Hospital of Qinghai Province, Xining, China.
Department of Central Lab, Cheeloo College of Medicine, Weihai Municipal Hospital, Shandong University, Weihai, China.
Cancer Sci. 2021 Aug;112(8):3190-3204. doi: 10.1111/cas.14987. Epub 2021 Jun 12.
Alterations of glycosyltransferase expression are often associated with tumor occurrence and progression. Among the many glycosyltransferases, increased expression of fucosyltransferase 8 (FUT8) has been frequently observed to be involved in progression and metastasis of various types of cancer. The regulatory mechanisms of FUT8 expression remain unclear. FUT8 expression was shown, in this study, to be elevated in breast cancer. Systematic analysis revealed that transcription factor activator protein 2γ (AP-2γ) is the target gene of microRNA-10b (miR-10b), which we previously identified as a positive regulator of FUT8. Overexpression of AP-2γ inhibited FUT8 expression, with associated reduction of cell invasiveness and migration ability. AP-2γ was capable of binding to transcription factor STAT3, and phosphorylation of STAT3 induced transcription of the FUT8 gene. On the basis of our findings, we propose that binding of AP-2γ to STAT3 results in formation of the AP-2γ/STAT3 complex and consequent inhibition of STAT3 phosphorylation, thereby preventing entry of p-STAT3 into the nucleus to initiate FUT8 transcription. This study clarifies the molecular mechanisms whereby transcription factor AP-2γ regulates FUT8 expression in breast cancer.
糖基转移酶表达的改变常与肿瘤的发生和发展有关。在众多糖基转移酶中,岩藻糖基转移酶 8(FUT8)的表达增加常与多种类型癌症的进展和转移有关。FUT8 表达的调控机制尚不清楚。本研究表明,FUT8 在乳腺癌中表达上调。系统分析显示,转录因子激活蛋白 2γ(AP-2γ)是 microRNA-10b(miR-10b)的靶基因,miR-10b 是我们之前鉴定的 FUT8 的正向调控因子。AP-2γ 的过表达抑制了 FUT8 的表达,同时降低了细胞的侵袭和迁移能力。AP-2γ 能够与转录因子 STAT3 结合,STAT3 的磷酸化诱导 FUT8 基因的转录。基于我们的发现,我们提出 AP-2γ 与 STAT3 的结合导致 AP-2γ/STAT3 复合物的形成,从而抑制 STAT3 的磷酸化,阻止 p-STAT3 进入细胞核启动 FUT8 转录。本研究阐明了转录因子 AP-2γ 调节乳腺癌中 FUT8 表达的分子机制。