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Alterations in expression, proteolysis and intracellular localizations of clusterin in esophageal squamous cell carcinoma

机译:食管鳞状细胞癌中簇蛋白表达,蛋白水解和细胞内定位的变化

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AIM: To investigate biogenesis and intracellular localizations of clusterin to elucidate the potential molecular mechanisms implicated in tumorigenesis of esophageal mucosa. METHODS: Semi-quantitative RT-PCR for multi-region alteration analysis, Western blot for different transcriptional forms and immunohistochemical staining for intracellular localizations of clusterin were carried out in both tissues and cell lines of ESCC. RESULTS: The N-terminal deletions of the clusterin gene and the appearance of a 50-53 ku nuclear clusterin, an uncleaved, nonglycosylated, and disulfide-linked isoform, were the major alterations in cancer cells of esophagus. Naturally the 40 ku clusterin was located in the connective tissue of the lamina propria of epithelial mucosa and right under the basal membrane of epithelia, but it was disappeared in stromal mucosa of esophagus and the pre-matured clusterin was found positive in cancerous epithelia. CONCLUSION: The N-terminal deletion of clusterin may be essential for its alterations of biogenesis in ESCC.
机译:目的:研究簇蛋白的生物发生和细胞内定位,以阐明与食管粘膜肿瘤发生有关的潜在分子机制。方法:在ESCC的组织和细胞系中进行了多区域改变分析的半定量RT-PCR,不同转录形式的Western印迹分析和簇蛋白胞内定位的免疫组化染色。结果:簇蛋白基因的N末端缺失和50-53 ku核簇蛋白的未切割,未糖基化和二硫键连接的亚型的出现是食道癌细胞的主要改变。自然地,40 ku簇蛋白位于上皮粘膜固有层的结缔组织中,并在上皮基底膜的正下方,但在食管的基质粘膜中消失,并且在癌性上皮中发现成熟的簇蛋白呈阳性。结论:簇蛋白N端缺失可能是ESCC生物发生改变的关键。

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