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关晓英, 王芙蓉. 胃黏膜瘤变过程中差异蛋白的表达[J]. 肿瘤防治研究, 2018, 45(8): 576-582. DOI: 10.3971/j.issn.1000-8578.2018.17.1439
引用本文: 关晓英, 王芙蓉. 胃黏膜瘤变过程中差异蛋白的表达[J]. 肿瘤防治研究, 2018, 45(8): 576-582. DOI: 10.3971/j.issn.1000-8578.2018.17.1439
GUAN Xiaoying, WANG Furong. Proteomics Research on Gastric Intraepithelial Neoplasia[J]. Cancer Research on Prevention and Treatment, 2018, 45(8): 576-582. DOI: 10.3971/j.issn.1000-8578.2018.17.1439
Citation: GUAN Xiaoying, WANG Furong. Proteomics Research on Gastric Intraepithelial Neoplasia[J]. Cancer Research on Prevention and Treatment, 2018, 45(8): 576-582. DOI: 10.3971/j.issn.1000-8578.2018.17.1439

胃黏膜瘤变过程中差异蛋白的表达

Proteomics Research on Gastric Intraepithelial Neoplasia

  • 摘要:
    目的 探讨胃癌发生发展的不同阶段(正常胃黏膜组织、反应性增生、低级别上皮内瘤变、高级别上皮内瘤变及黏膜内腺癌)差异蛋白的表达。
    方法 以胃窦部肠型胃癌为研究对象,选取正常、反应性增生、低/高级别上皮内瘤变、黏膜内癌5组各30例共150例组织标本,用非标记蛋白质组学(label-free)联合液性色谱质谱(LC-MC/MC)筛选差异蛋白,并评估差异蛋白潜在的生物学功能。
    结果 筛选出了8个差异蛋白,和正常黏膜相比,在低级别上皮内瘤变—高级别上皮内瘤变及黏膜内癌的发展过程中,LAMN1、ERGIC1、UQCRFS1、UQCRH和CISD1这5个蛋白质的表达量逐渐降低,表达量逐渐升高的蛋白质有HMGB1、DNA-PKcs和14-3-3。
    结论 在胃癌发生发展的不同阶段,蛋白质的表达存在明显的差异,这些差异蛋白具有成为胃癌早期诊断及靶向分子治疗标志物的潜能。

     

    Abstract:
    Objective To investigate the expression of differential proteins in the typical process of gastric intraepithelial neoplasia including normal gastric antrum mucosa, reactive hyperplasia, low-grade intraepithelial neoplasia, high-grade intraepithelial neoplasia and intramucosal carcinoma.
    Methods We enrolled 150 specimens of different stages of gastric tissues, including normal gastric antrum mucosa, reactive hyperplasia, low-grade intraepithelial neoplasia, high-grade intraepithelial neoplasia and early gastric cancer(each n=30). The expression profiles of total proteins were detected by label-free quantification technology integrated with liquid chromatography-tandem mass spectrometry (LC-MS/MS). Potential biological function of differential proteins was analyzed.
    Results We screened out eight differential proteins. Compared with normal gastric antrum mucosa, during the process of gastric intraepithelial neoplasia including low-grade intraepithelial neoplasia, high-grade intraepithelial neoplasia and intramucosal carcinoma, the expression of five proteins LAMN1, ERGIC1, UQCRFS1, UQCRH, CISD1 gradually decreased, and three proteins with increasing expressions were HMGB1, DNA-PKcs, 14-3-3.
    Conclusion There are many proteins expressed differently in different stages of gastric cancer. They might be expected to be novel early diagnostic and targeted therapeutic biomarkers.

     

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