首页> 外文期刊>Molecular cancer research: MCR >Ketogenic HMGCS2 Is a c-Myc target gene expressed in differentiated cells of human colonic epithelium and down-regulated in colon cancer.
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Ketogenic HMGCS2 Is a c-Myc target gene expressed in differentiated cells of human colonic epithelium and down-regulated in colon cancer.

机译:生酮HMGCS2是一种c-Myc靶基因,在人结肠上皮细胞中表达,并在结肠癌中下调。

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摘要

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.
机译:HMGCS2是调节酮体生成的基因,在肝脏和一些肝外组织(例如结肠)中表达。在CaCo-2结肠上皮细胞中,该基因的表达随细胞分化而增加。因此,用特异性抗体的免疫组织化学显示HMGCS2主要在人结肠上皮的分化细胞中表达。在这里,我们使用染色质免疫沉淀实验来研究负责这种表达模式的分子机制。该测定表明,HMGCS2是c-Myc的直接靶标,可抑制HMGCS2的转录活性。 c-Myc的阻遏作用是通过阻止Miz-1的反式激活而介导的,Miz-1的反式激活主要通过基因的近端启动子中的Sp1结合位点发生。因此,在90%的Myc依赖性结肠和直肠肿瘤中,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。另外,它在80%的小肠Myc非依赖性肿瘤中也下调。基于这些发现,我们提出,生酮作用是增殖细胞的不良代谢特征,其通过c-Myc介导的关键代谢基因HMGCS2的抑制而下调。

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