首页> 外文期刊>Oncology reports >Proteomics-based identification of a tumor-associated antigen and its corresponding autoantibody in gastric cancer.
【24h】

Proteomics-based identification of a tumor-associated antigen and its corresponding autoantibody in gastric cancer.

机译:基于蛋白质组学的胃癌中肿瘤相关抗原及其相应自身抗体的鉴定。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Identification of novel tumor-related antigens and autoantibodies will lead to early diagnosis of cancer and the development of more effective immunotherapies. The purpose of this study was to identify novel tumor antigens from the gastric cancer cell lines MkN-1, MkN-45 and KATOIII, and their related autoantibodies in sera of patients with gastric cancer using a proteomics-based approach. Proteins from the gastric cancer cell lines (MkN-1, MkN-45 and KATOIII) were separated by two-dimensional polyacrylamide gel electrophoresis, followed by Western blotting and antibody reaction with sera from patients with gastric cancer, healthy individuals and patients with other cancers. Positive spots were excised from Coomassie blue stained gels and analyzed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF/TOF MS). Sera from patients with gastric cancer yielded multiple spots, one of which was identified as the 78 kDa glucose-regulated protein (GRP78) by MALDI-TOF/TOF MS. Western blots against recombinant GRP78 showed reactivity in sera from 17/60 (28.3%) patients with gastric cancer and 0/20 (0.0%) of healthy individuals. Autoantibodies against GRP78 were found in 4/15 (26.7%) and 3/15 (20.0%) patients with esophageal and colon cancer, respectively. We identified for the first time an autoantibody against GRP78 in gastric cancer patients. The proteomic approach implemented in this study offers a powerful tool for identifying novel serum markers that may display clinical usefulness in cancer.
机译:新的肿瘤相关抗原和自身抗体的鉴定将导致癌症的早期诊断和更有效的免疫疗法的发展。这项研究的目的是使用蛋白质组学方法从胃癌患者血清中鉴定出胃癌细胞MkN-1,MkN-45和KATOIII的新型肿瘤抗原及其相关自身抗体。通过二维聚丙烯酰胺凝胶电泳分离胃癌细胞株(MkN-1,MkN-45和KATOIII)中的蛋白质,然后进行蛋白质印迹和与胃癌患者,健康个体和其他癌症患者血清的抗体反应。从考马斯亮兰色凝胶切出阳性斑点,并通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF / TOF MS)进行分析。来自胃癌患者的血清产生多个斑点,其中一个斑点被MALDI-TOF / TOF MS鉴定为78 kDa葡萄糖调节蛋白(GRP78)。针对重组GRP78的Western印迹显示17/60(28.3%)胃癌患者和0/20(0.0%)健康个体的血清具有反应性。分别在4/15(26.7%)和3/15(20.0%)的食道癌和结肠癌患者中发现了针对GRP78的自身抗体。我们首次在胃癌患者中鉴定了针对GRP78的自身抗体。在这项研究中实施的蛋白质组学方法提供了一个强大的工具,可用于识别可能在癌症中显示出临床实用性的新型血清标志物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号