Camarero Nuria, Mascaró Cristina, Mayordomo Cristina, Vilardell Felip, Haro Diego, Marrero Pedro F
Department of Biochemistry and Molecular Biology, School of Pharmacy, University of Barcelona, E-08028 Barcelona, Spain.
Mol Cancer Res. 2006 Sep;4(9):645-53. doi: 10.1158/1541-7786.MCR-05-0267. Epub 2006 Aug 28.
HMGCS2, the gene that regulates ketone body production, is expressed in liver and several extrahepatic tissues, such as the colon. In CaCo-2 colonic epithelial cells, the expression of this gene increases with cell differentiation. Accordingly, immunohistochemistry with specific antibodies shows that HMGCS2 is expressed mainly in differentiated cells of human colonic epithelium. Here, we used a chromatin immunoprecipitation assay to study the molecular mechanism responsible for this expression pattern. The assay revealed that HMGCS2 is a direct target of c-Myc, which represses HMGCS2 transcriptional activity. c-Myc transrepression is mediated by blockade of the transactivating activity of Miz-1, which occurs mainly through a Sp1-binding site in the proximal promoter of the gene. Accordingly, the expression of human HMGCS2 is down-regulated in 90% of Myc-dependent colon and rectum tumors. HMGCS2 protein expression is down-regulated preferentially in moderately and poorly differentiated carcinomas. In addition, it is also down-regulated in 80% of small intestine Myc-independent tumors. Based on these findings, we propose that ketogenesis is an undesirable metabolic characteristic of the proliferating cell, which is down-regulated through c-Myc-mediated repression of the key metabolic gene HMGCS2.
HMGCS2是一种调节酮体生成的基因,在肝脏和一些肝外组织(如结肠)中表达。在CaCo-2结肠上皮细胞中,该基因的表达随着细胞分化而增加。因此,用特异性抗体进行免疫组织化学分析表明,HMGCS2主要在人结肠上皮的分化细胞中表达。在此,我们使用染色质免疫沉淀分析来研究导致这种表达模式的分子机制。该分析表明,HMGCS2是c-Myc的直接靶标,c-Myc可抑制HMGCS2的转录活性。c-Myc的反式抑制作用是通过阻断Miz-1的反式激活活性介导的,这主要通过该基因近端启动子中的一个Sp1结合位点发生。因此,在90%的依赖Myc的结肠和直肠肿瘤中,人HMGCS2的表达下调。HMGCS2蛋白表达在中度和低分化癌中优先下调。此外,在80%的不依赖Myc的小肠肿瘤中其表达也下调。基于这些发现,我们提出酮生成是增殖细胞一种不良的代谢特征,它通过c-Myc介导的对关键代谢基因HMGCS2的抑制而下调。