Plasma protein profiling in a stage defined pancreatic cancer cohort - Implications for early diagnosis

被引:23
作者
Gerdtsson, Anna Sandstrom [1 ]
Wingren, Christer [1 ]
Persson, Helena [1 ]
Delfani, Payam [1 ]
Nordstrom, Malin [2 ]
Ren, He [3 ]
Wen, Xin [3 ]
Ringdahl, Ulrika [1 ]
Borrebaeck, Carl A. K. [1 ]
Hao, Jihui [3 ]
机构
[1] Lund Univ, CREATE Hlth Translat Canc Ctr, Dept Immunotechnol, Medicon Village Bldg 406, SE-22381 Lund, Sweden
[2] Immunovia AB, SE-22381 Lund, Sweden
[3] Tianjin Med Univ Canc Inst & Hosp, Huan Hu Xi Rd, Tianjin 300060, Peoples R China
关键词
Pancreatic cancer; Biomarker signatures; Early detection; Antibody microarrays; Recombinant antibodies; RECOMBINANT ANTIBODY MICROARRAYS; BIOMARKER PANELS; CT SCANS; EXPRESSION; CARCINOMA; DESIGN; GROWTH; ONSET; ADENOCARCINOMA; OVEREXPRESSION;
D O I
10.1016/j.molonc.2016.07.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) is a disease where detection preceding clinical symptoms significantly increases the life expectancy of patients. In this study, a recombinant antibody microarray platform was used to analyze 213 Chinese plasma samples from PDAC patients and normal control (NC) individuals. The cohort was stratified according to disease stage, i.e. resectable disease (stage I/II), locally advanced (stage III) and metastatic disease (stage IV). Support vector machine analysis showed that all PDAC stages could be discriminated from controls and that the accuracy increased with disease progression, from stage I to IV. Patients with stage I/II PDAC could be discriminated from NC with high accuracy based on a plasma protein signature, indicating a possibility for early diagnosis and increased detection rate of surgically resectable tumors. (C) 2016 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1305 / 1316
页数:12
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