Department of General Surgery, Shengjing Hospital of China Medical University, Shenyang, China.
Department of General Surgery, Shengjing Hospital of China Medical University, Shenyang, China.
Am J Pathol. 2021 Dec;191(12):2117-2132. doi: 10.1016/j.ajpath.2021.08.010. Epub 2021 Sep 8.
The karyopherin α subunit gene (KPNA2), an oncogene, is involved in metabolic reprogramming in cancer. This study aimed to explore the function of KPNα in the growth and glycolysis in colon cancer (CC) cells. Genes from the Oncomine database that were differentially expressed in multiple CC types were screened. Bioinformatics analysis suggested that KPNA2 was highly expressed in CC, and consequently, high expression of KPNA2 was detected in the CC cell lines. Down-regulation of KPNA2 reduced viability and DNA-replication ability, and increased apoptosis of HCT116 and LoVo cells. It also reduced glucose consumption, extracellular acidification rate, and the ATP production in cells. Centromere protein A (CENPA) was confirmed as an upstream transcription activator of KPNA2. There was significant H3K27ac modification in the promoter region of KPNA2. CENPA primarily recruited histone acetyltransferase general control of amino acid synthesis (GCN)-5 to the promoter region of KPNA2 to induce transcription activation. Overexpression of either CENPA or GCN-5 blocked the role of short hairpin KPNα and restored growth and glycolysis in CC cells. To conclude, the findings from this study suggest that CENPA recruits GCN-5 to the promoter region of KPNA2 to induce KPNα activation, which strengthens growth and glycolysis in, and augments the development of, CC.
核输出蛋白 α 亚基基因(KPNA2)是一种癌基因,参与癌症中的代谢重编程。本研究旨在探索 KPNα 在结肠癌细胞(CC)生长和糖酵解中的功能。从多个 CC 类型的 Oncomine 数据库中筛选出差异表达的基因。生物信息学分析表明 KPNA2 在 CC 中高表达,因此在 CC 细胞系中检测到 KPNA2 的高表达。下调 KPNA2 降低了 HCT116 和 LoVo 细胞的活力和 DNA 复制能力,并增加了细胞凋亡。它还降低了细胞中的葡萄糖消耗、细胞外酸化率和 ATP 产生。着丝粒蛋白 A(CENPA)被证实为 KPNA2 的上游转录激活物。KPNA2 启动子区域存在显著的 H3K27ac 修饰。CENPA 主要将组蛋白乙酰转移酶一般氨基酸合成的整体控制(GCN)-5募集到 KPNA2 的启动子区域,以诱导转录激活。CENPA 或 GCN-5 的过表达均可阻断短发夹 KPNα 的作用,并恢复 CC 细胞的生长和糖酵解。总之,本研究的结果表明,CENPA 将 GCN-5 募集到 KPNA2 的启动子区域,诱导 KPNα 激活,从而增强 CC 的生长和糖酵解,并促进其发展。