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首页> 外文期刊>Journal of proteomics >Discovery of potential colorectal cancer serum biomarkers through quantitative proteomics on the colonic tissue interstitial fluids from the AOM-DSS mouse model
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Discovery of potential colorectal cancer serum biomarkers through quantitative proteomics on the colonic tissue interstitial fluids from the AOM-DSS mouse model

机译:通过定量蛋白质组学从AOM-DSS小鼠模型结肠组织间质液中发现潜在的结直肠癌血清生物标志物

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Quantitative proteomic analysis was performed using iTRAQ to discover colorectal cancer (CRC)-related proteins in tissue interstitial fluids (TIFs). A typical inflammation-related CRC mouse model was generated using azoxymethane dextran sodium sulfate (AOM-DSS), and TIF5 were collected from these mice in four stages during CRC development. Using stringent criteria, a total of 144 proteins displayed changes in their abundances during tumor growth, including 45 that consecutively increased, 17 that consecutively decreased and 82 that changed irregularly. Of these 144 proteins, 24 of the consecutively changed proteins were measured using MRM in individual TIF samples, and 18 were verified. Twelve proteins verified to be consecutively increased in TIFs were examined using MRM to evaluate changes in their abundance in individual mouse serum samples. The abundances of leucine-rich alpha-2-glycoprotein 1 (LRG1), tubulin beta-5 chain (TUBB5) and immunoglobulin J chain (IGJ) were significantly higher in CRC mice than in control mice. Using clinical samples and MRM, we further verified that LRG1 and TUBB5 are potential CRC serum biomarkers. These data demonstrate that coupling dynamic TIF proteomics with targeted serum proteomics in an animal model is a promising avenue for pursuing the discovery of tumor serum biomarkers.
机译:使用iTRAQ进行了定量蛋白质组分析,以发现组织间质液(TIF)中与结肠直肠癌(CRC)相关的蛋白质。使用乙氧基甲烷葡聚糖硫酸钠(AOM-DSS)生成典型的炎症相关CRC小鼠模型,并在CRC发育的四个阶段从这些小鼠中收集TIF5。使用严格的标准,总共144种蛋白质在肿瘤生长过程中表现出丰度变化,包括45种连续增加,17种连续减少和82种不规则变化。在这144种蛋白质中,使用MRM在单个TIF样品中测量了24种连续变化的蛋白质,并验证了18种。使用MRM检查了12种在TIF中连续增加的蛋白质,以评估其在单个小鼠血清样品中的丰度变化。 CRC小鼠中富含亮氨酸的α-2-糖蛋白1(LRG1),微管蛋白β-5链(TUBB5)和免疫球蛋白J链(IGJ)的丰度明显高于对照组。使用临床样本和MRM,我们进一步验证了LRG1和TUBB5是潜在的CRC血清生物标志物。这些数据表明,在动物模型中将动态TIF蛋白质组学与靶向血清蛋白质组学结合起来是寻找肿瘤血清生物标记物的有希望的途径。

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