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Down-regulation of the phosphoenolpyruvate carboxykinase gene in human colon tumors and induction by omega-3 fatty acids

机译:人结肠肿瘤中磷酸烯醇丙酮酸羧激酶基因的下调和omega-3脂肪酸的诱导

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摘要

The polyunsaturated fatty acid (PUFA) docosahexaenoic acid (DHA) reduces proliferation of several cell types, including colon tumor cells, and regulates gene expression in a cell- and gene-selective manner. In hepatocytes, the fatty acid synthase (FAS) gene is down-regulated by DHA whereas the carnitine pal-mitoyltransferase-1 (CPT-1) gene is up-regulated. In adipocytes but not in hepatocytes, the expression of the cytosolic phosphoenolpyruvate carboxykinase (PEPCK-C) gene is stimulated by unsaturated FA, including DHA. We monitored the expression of the FAS, CPT-1 and PEPCK-C genes in rat and human colon and in colonic tumors from humans. The ratio of PEPCK-C to FAS transcripts was in favor of PEPCK-C in human and rat colon, whereas the opposite occurred in Caco2 tumoral cells. FAS gene expression declined from proliferative to differentiated Caco2 cells, while in contrast the expression of PEPCK-C and CPT-1 genes increased. DHA strongly induced expression of the PEPCK-C and CPT-1 genes, in correlation with decreased cell growth, while, as expected, it reduced FAS mRNA. We assessed the relative expression of PEPCK-C, CPT-1 and FAS genes in fragments of colonic tumors and adjacent non-tumoral tissue from a series of 10 patients. PEPCK-C and CPT-1 mRNAs are more abundant in non-tumoral tissues than in the tumoral counterpart, whereas the opposite occurred for the FAS gene. Therefore, the PEPCK-C gene can be defined as a new negative marker for colonic tumors and a target for the anti-tumorigenic action of omega-3 PUFAs.
机译:多不饱和脂肪酸(PUFA)二十二碳六烯酸(DHA)减少了几种细胞类型(包括结肠肿瘤细胞)的增殖,并以细胞和基因选择性的方式调节基因表达。在肝细胞中,脂肪酸合成酶(FAS)基因被DHA下调,而肉碱pal-mitoyltransferase-1(CPT-1)基因被上调。在脂肪细胞中而不在肝细胞中,胞质磷酸烯醇丙酮酸羧化激酶(PEPCK-C)基因的表达受到不饱和脂肪酸(包括DHA)的刺激。我们监测了FAS,CPT-1和PEPCK-C基因在大鼠和人类结肠以及人类结肠肿瘤中的表达。 PEPCK-C与FAS转录本的比例有利于人和大鼠结肠中的PEPCK-C,而相反的情况发生在Caco2肿瘤细胞中。 FAS基因表达从增生的Caco2细胞下降到分化的Caco2细胞,相反,PEPCK-C和CPT-1基因的表达增加。 DHA强烈诱导了PEPCK-C和CPT-1基因的表达,与细胞生长减少相关,而正如所预期的,它减少了FAS mRNA。我们评估了PEPCK-C,CPT-1和FAS基因在一系列10例患者的结肠肿瘤和邻近非肿瘤组织的片段中的相对表达。 PEPCK-C和CPT-1 mRNA在非肿瘤组织中比在肿瘤对应物中更为丰富,而FAS基因则相反。因此,可以将PEPCK-C基因定义为结肠肿瘤的新阴性标记,并作为omega-3 PUFA的抗肿瘤发生作用的靶标。

著录项

  • 来源
    《Biochimie》 |2010年第12期|p.1772-1777|共6页
  • 作者单位

    Institut National de la Santi et de la Recherche Medicate UMR-S 747, Universite Paris Descartes, Pharmacologie Toxicologie et Signalisation Cellulaire,45 rue des Saints-Peres, 75006 Paris, France;

    Institut National de la Santi et de la Recherche Medicate UMR-S 747, Universite Paris Descartes, Pharmacologie Toxicologie et Signalisation Cellulaire,45 rue des Saints-Peres, 75006 Paris, France;

    Institut National de la Sante et de la Recherche Medicate UMR-S 775, Universite Paris Descartes, Bases Moleculaires de la Response aux Xenobiotiques,45 rue des Saints-Peres, 75006 Paris, France;

    Institut National de la Santi et de la Recherche Medicate UMR-S 747, Universite Paris Descartes, Pharmacologie Toxicologie et Signalisation Cellulaire,45 rue des Saints-Peres, 75006 Paris, France;

    Institut National de la Santi et de la Recherche Medicate UMR-S 747, Universite Paris Descartes, Pharmacologie Toxicologie et Signalisation Cellulaire,45 rue des Saints-Peres, 75006 Paris, France;

    Institut National de la Sante et de la Recherche Medicate UMR-S 775, Universite Paris Descartes, Bases Moleculaires de la Response aux Xenobiotiques,45 rue des Saints-Peres, 75006 Paris, France;

    Institut National de la Santi et de la Recherche Medicate UMR-S 747, Universite Paris Descartes, Pharmacologie Toxicologie et Signalisation Cellulaire,45 rue des Saints-Peres, 75006 Paris, France;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    colon cancer; omega-3; FAS; CPT-1; PEPCK;

    机译:结肠癌;欧米加3;FAS;CPT-1;聚氯乙烯;
  • 入库时间 2022-08-18 01:24:04

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