结直肠癌
蛋白质组学
小桶
肿瘤科
定量蛋白质组学
癌症
生物信息学
医学
内科学
疾病
生物标志物
癌症研究
生物
蛋白质组
血液蛋白质类
队列
基因表达谱
计算生物学
蛋白质表达
基因
信使核糖核酸
个性化医疗
转录组
基因表达
肿瘤进展
作者
Qi Zhang,Wenyuan Zhu,Liya Wei,Jian Shen,Minzhe Li,Jianguo Ji,Qingsong Wang
标识
DOI:10.1021/acs.jproteome.5c00651
摘要
Colorectal cancer (CRC) is an aggressive malignant tumor of the digestive system that poses a serious threat to human health. Therefore, there is an urgent need to discover early diagnostic markers and effective therapeutic targets for CRC. In this study, data independent acquisition (DIA) mass spectrometry quantitative technology combined with bioinformatics analysis was used to carry out personalized quantitative proteomics research on abundant protein depletion plasma samples from 48 CRC patients at different TNM stages and healthy individuals. A total of 1089 Protein Groups were identified. By comparing the plasma protein expression profiles between CRC patients and healthy individuals, differentially expressed proteins (DEPs) CRP, FABP1, FABP4 and OSTP with significant changes were screened out, and GO functional, KEGG pathway, and GSEA enrichment analysis were performed. Mfuzz clustering analysis categorized the DEPs in CRC plasma into six expression patterns. Among them, the OSTP protein level in proteomics data and the mRNA level of the gene spp1 in TCGA database both showed an upward trend with the progression of the disease, suggesting that it may serve as a diagnostic and prognostic marker in plasma to reflect the disease progression of CRC patients. ROC analysis showed robust predictive performance, and PRM validation cohort correlated well with DIA results, providing potential insights for CRC research.
科研通智能强力驱动
Strongly Powered by AbleSci AI