Ren Qianwen, Xiang Meiyi, Qiao Juanli, Liu Zhaojun, Zhang Ge, Gu Liankun, Zhou Jing, Tian Wei, Deng Dajun
Key Laboratory of Carcinogenesis and Translational Research (MOE/Beijing), Division of Etiology, Peking University Cancer Hospital and Institute, Beijing, 100142, China.
Int J Biol Sci. 2025 Jan 13;21(3):1127-1143. doi: 10.7150/ijbs.102431. eCollection 2025.
TTC7B is the PI4KA-binding protein. The upstream regulatory network associated with the expression of genes involved in RNA N6-adenine (m6A) methylation is not clear. Bioinformatics analysis revealed that the expression levels of , , and are positively correlated with each other across human tissues. These genes are consistently downregulated in many cancers. We initially confirmed the correlation of the expression of these genes in colon cancer tissues from patients (n=105) and reported that downregulation was significantly associated with poor prognosis. We subsequently performed a series of biological experiments and demonstrated that TTC7B upregulated RXRA expression probably through the PI4KA-mediated AKT1 pathway and that RXRA was a transcription factor for the gene. TTC7B inhibited the proliferation of colon cancer cells by increasing the recruitment of RXRA to the promoter, increasing expression, and decreasing the total RNA m6A level. Ablation of demethylase activity completely abolished the inhibitory effect of on the proliferation of cancer cells and . In conclusion, our study demonstrated for the first time that TTC7B triggers the RXRA-FTO axis through PI4KA binding, which leads to a decrease in total RNA m6A modification and the inhibition of colon cancer progression.
TTC7B是与PI4KA结合的蛋白。与RNA N6-腺嘌呤(m6A)甲基化相关基因表达的上游调控网络尚不清楚。生物信息学分析显示,在人体组织中,[此处原文缺失具体基因名称]、[此处原文缺失具体基因名称]和[此处原文缺失具体基因名称]的表达水平彼此呈正相关。这些基因在许多癌症中持续下调。我们最初在105例患者的结肠癌组织中证实了这些基因表达的相关性,并报告[此处原文缺失具体基因名称]下调与预后不良显著相关。随后,我们进行了一系列生物学实验,证明TTC7B可能通过PI4KA介导的AKT1途径上调RXRA表达,且RXRA是[此处原文缺失具体基因名称]基因的转录因子。TTC7B通过增加RXRA与[此处原文缺失具体基因名称]启动子的结合、增加[此处原文缺失具体基因名称]表达以及降低总RNA m6A水平来抑制结肠癌细胞的增殖。消除[此处原文缺失具体基因名称]去甲基酶活性完全消除了[此处原文缺失具体基因名称]对癌细胞[此处原文缺失具体癌细胞名称]和[此处原文缺失具体癌细胞名称]增殖的抑制作用。总之,我们的研究首次证明TTC7B通过PI4KA结合触发RXRA-FTO轴,导致总RNA m6A修饰减少并抑制结肠癌进展。