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Expression and the role of 3′-phosphoadenosine 5′-phosphosulfate transporters in human colorectal carcinoma

机译:3'-磷酸腺苷5'-磷酸硫酸盐转运蛋白在人大肠癌中的表达及其作用

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摘要

Sulfation represents an essential modification for various molecules and regulates many biological processes. The sulfation of glycans requires a specific transporter for 3′-phosphoadenosine 5′-phosphosulfate (PAPS) on the Golgi apparatus. This study investigated the expression of PAPS transporter genes in colorectal carcinomas and the significance of Golgi-specific sulfation in the proliferation of colorectal carcinoma cells. The relative amount of PAPST1 transcripts was found to be higher than those of PAPST2 in colorectal cancerous tissues. Immunohistochemically, the enhanced expression of PAPST1 was observed in fibroblasts in the vicinity of invasive cancer cells, whereas the expression of PAPST2 was decreased in the epithelial cells. RNA interference of either of the two PAPS transporter genes reduced the extent of sulfation of cellular proteins and cellular proliferation of DLD-1 human colorectal carcinoma cells. Silencing the PAPS transporter genes reduced fibroblast growth factor signaling in DLD-1 cells. These findings indicate that PAPS transporters play a role in the proliferation of colorectal carcinoma cells themselves and take part in a desmoplastic reaction to support cancer growth by controlling their sulfation status.
机译:硫酸化代表了各种分子的基本修饰,并调节许多生物学过程。聚糖的硫酸化需要高尔基体中3'-磷酸腺苷5'-磷酸硫酸盐(PAPS)的特定转运蛋白。这项研究调查了PAPS转运蛋白基因在大肠癌中的表达以及高尔基体特异性硫酸化在大肠癌细胞增殖中的意义。发现在大肠癌组织中PAPST1转录本的相对量高于PAPST2。免疫组织化学观察,在侵袭性癌细胞附近的成纤维细胞中观察到PAPST1的表达增强,而在上皮细胞中PAPST2的表达降低。两个PAPS转运蛋白基因之一的RNA干扰降低了细胞蛋白的硫酸化程度和DLD-1人结肠直肠癌细胞的细胞增殖。沉默PAPS转运蛋白基因可减少DLD-1细胞中的成纤维细胞生长因子信号传导。这些发现表明,PAPS转运蛋白在结直肠癌细胞本身的增殖中起作用,并参与去肿瘤反应,通过控制其硫酸化状态来支持癌症的生长。

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  • 来源
    《Glycobiology》 |2011年第2期|p.235-246|共12页
  • 作者

    Shoko Nishihara;

  • 作者单位

    Soka University, @%@, National Institute of Advanced Industrial Science and Technology (AIST), @%@, Osaka National Hospital, National Hospital Organization, @%@, National Institute of Radiological Sciences, @%@, Graduate School of Pharmaceutical Science;

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