Ketogenic HMGCS2 is a c-Myc target gene expressed in differentiated cells of human colonic epithelium and down-regulated in colon cancer

被引:76
作者
Camarero, Nuria
Mascaro, Cristina
Mayordomo, Cristina
Vilardell, Felip
Haro, Diego
Marrero, Pedro F. [1 ]
机构
[1] Univ Barcelona, Dept Biochem & Mol Biol, Sch Pharm, E-08028 Barcelona, Spain
[2] Inst Catala Oncol, Bellvitge Colorectal Canc Study Grp, Barcelona, Spain
关键词
D O I
10.1158/1541-7786.MCR-05-0267
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
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页码:645 / 653
页数:9
相关论文
共 52 条
[51]   ACTIVITY AND INTRACELLULAR DISTRIBUTION OF ENZYMES OF KETONE-BODY METABOLISM IN RAT LIVER [J].
WILLIAMS.DH ;
BATES, MW ;
KREBS, HA .
BIOCHEMICAL JOURNAL, 1968, 108 (03) :353-&
[52]   Induction of HDAC2 expression upon loss of APC in colorectal tumorigenesis [J].
Zhu, P ;
Martin, E ;
Mengwasser, J ;
Schlag, P ;
Janssen, KP ;
Göttlicher, M .
CANCER CELL, 2004, 5 (05) :455-463