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Mining novel biomarkers for prognosis of gastric cancer with serum proteomics

机译:利用血清蛋白质组学挖掘新型生物标志物用于胃癌预后

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Background Although gastric caner (GC) remains the second cause of cancer-related death, useful biomarkers for prognosis are still unavailable. We present here the attempt of mining novel biomarkers for GC prognosis by using serum proteomics. Methods Sera from 43 GC patients and 41 controls with gastritis as Group 1 and 11 GC patients as Group 2 was successively detected by Surface Enhanced Laser Desorption/ionization Time of Flight Mass Spectrometry (SELDI-TOF-MS) with Q10 chip. Peaks were acquired by Ciphergen ProteinChip Software 3.2.0 and analyzed by Zhejiang University-ProteinChip Data Analysis System (ZJU-PDAS). CEA level were evaluated by chemiluminescence immunoassay. Results After median follow-up periods of 33 months, Group 1 with 4 GC patients lost was divided into 20 good-prognosis GC patients (overall survival more than 24 months) and 19 poor-prognosis GC patients (no more than 24 months). The established prognosis pattern consisted of 5 novel prognosis biomarkers with 84.2% sensitivity and 85.0% specificity, which were significantly higher than those of carcinoembryonic antigen (CEA) and TNM stage. We also tested prognosis pattern blindly in Group 2 with 66.7% sensitivity and 80.0% specificity. Moreover, we found that 4474-Da peak elevated significantly in GC and was associated with advanced stage (III+IV) and short survival (p Conclusion We have identified a number of novel biomarkers for prognosis prediction of GC by using SELDI-TOF-MS combined with sophisticated bioinformatics. Particularly, elevated expression of 4474-Da peak showed very promising to be developed into a novel biomarker associated with biologically aggressive features of GC.
机译:背景尽管胃癌(GC)仍然是癌症相关死亡的第二大原因,但仍缺乏用于预后的有用生物标志物。我们在这里提出了通过使用血清蛋白质组学来挖掘用于GC预后的新型生物标志物的尝试。方法采用Q10芯片通过表面增强激光解吸/电离飞行时间质谱(SELDI-TOF-MS)相继检测43例胃癌患者和41例胃炎对照组患者(第1组)和11例胃癌患者(第2组)的血清。使用Ciphergen ProteinChip软件3.2.0采集峰,并通过浙江大学-ProteinChip数据分析系统(ZJU-PDAS)进行分析。通过化学发光免疫测定法评估CEA水平。结果在中位随访33个月后,将4例GC患者丢失的第1组分为20例预后良好的GC患者(总生存期超过24个月)和19例预后不良的GC患者(不超过24个月)。建立的预后模式包括5种新颖的预后生物标志物,敏感性为84.2%,特异性为85.0%,显着高于癌胚抗原(CEA)和TNM分期。我们还在第2组中盲检测了预后模式,敏感性为66.7%,特异性为80.0%。此外,我们发现4474-Da峰在GC中显着升高,并与晚期(III + IV)和短期生存有关(p结论)我们已经通过使用SELDI-TOF-MS鉴定了许多可用于GC预后预测的新生物标志物特别是4474-Da峰的高表达显示出非常有希望的发展成与GC的生物学侵袭性特征相关的新型生物标志物。

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