前列腺组织中的靶向蛋白质组学方法:一组潜在的癌症检测生物标志物

D. Aiello, Francesca Casadonte, R. Terracciano, R. Damiano, R. Savino, G. Sindona, A. Napoli
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引用次数: 33

摘要

前列腺癌(PCa)是男性癌症相关死亡的第六大原因。其行为和进化背后的分子事件尚不完全清楚。前列腺特异性抗原(PSA)是美国食品和药物管理局唯一批准的生物标志物。一组来自前列腺癌患者的10个分期特异性肿瘤和邻近非肿瘤组织(Gleason评分6,3 +3;采用MS-based蛋白质组学方法检测PSA 10 ÷19 ng/ml。该方法基于对组织中碱基可溶性蛋白的鉴定,建立了一种高效的研究方法,从分子角度对PCa有了更深入的了解。共发现164个蛋白,其中132个在肿瘤组织中被评估为差异表达。匠人途径分析(Ingenuity Pathway Analysis, IPA)显示,在获得的所有数据集中,105个分子与上皮瘤变有关,p值为3.62 -05,而仅检测到11个分子归因于前哨组织和体液。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted proteomic approach in prostatic tissue: a panel of potential biomarkers for cancer detection
Prostate cancer (PCa) is the sixth highest causes of cancer-related deaths in men. The molecular events underlying its behavior and evolution are not completely understood. Prostate-specific antigen (PSA) is the only approved Food and Drug Administration biomarker. A panel of ten stage-specific tumoral and adjacent non tumoral tissues from patients affected by PCa (Gleason score 6, 3+3; PSA 10 ÷19 ng/ml) was investigated by MS-based proteomics approach. The proposed method was based on identifying the base-soluble proteins from tissue, established an efficient study, which lead to a deeper molecular perspective understanding of the PCa. A total of 164 proteins were found and 132 of these were evaluated differentially expressed in tumoral tissues. The Ingenuity Pathway Analysis (IPA) showed that among all dataset obtained, 105 molecules were involved in epithelial neoplasia with a p-value of 3.62E-05, whereas, only 11 molecules detected were ascribed to sentinel tissue and bodily fluids.
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