结直肠癌
蛋白质组学
癌症
病理
生物
癌症研究
计算生物学
医学
肿瘤科
内科学
生物化学
基因
作者
Ana Montero‐Calle,María Garranzo‐Asensio,Carmen Povés,Rodrigo Sanz,Jana Dziaková,Alberto Peláez‐García,Vivian de los Rı́os,Javier Martínez‐Useros,María Jesús Fernández‐Aceñero,Rodrigo Barderas
标识
DOI:10.1021/acs.jproteome.3c00749
摘要
A deeper understanding of colorectal cancer (CRC) biology would help to identify specific early diagnostic markers. Here, we conducted quantitative proteomics on FFPE healthy, adenoma, and adenocarcinoma tissue samples from six stage I sporadic CRC patients to identify dysregulated proteins during early CRC development. Two independent quantitative 10-plex TMT experiments were separately performed. After protein extraction, trypsin digestion, and labeling, proteins were identified and quantified by using a Q Exactive mass spectrometer. A total of 2681 proteins were identified and quantified after data analysis and bioinformatics with MaxQuant and the R program. Among them, 284 and 280 proteins showed significant upregulation and downregulation (expression ratio ≥1.5 or ≤0.67,
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