Serum IGFBP2 and MSLN as diagnostic and prognostic biomarkers for pancreatic cancer

被引:64
作者
Kendrick, Zachary W. [1 ]
Firpo, Matthew A. [1 ,4 ]
Repko, Robert C. [1 ]
Scaife, Courtney L. [1 ,4 ]
Adler, Douglas G. [2 ,4 ]
Boucher, Kenneth M. [3 ,4 ]
Mulvihill, Sean J. [1 ,4 ]
机构
[1] Univ Utah, Dept Surg, Sch Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Dept Internal Med, Sch Med, Salt Lake City, UT 84132 USA
[3] Univ Utah, Dept Oncol Sci, Sch Med, Salt Lake City, UT 84132 USA
[4] Huntsman Canc Inst, Salt Lake City, UT USA
基金
美国国家卫生研究院;
关键词
MEGAKARYOCYTE POTENTIATING FACTOR; DUCTAL ADENOCARCINOMAS; OVARIAN-CANCER; MESOTHELIN; INVASION; METASTASIS; ACTIVATION; EXPRESSION; BINDING; UTILITY;
D O I
10.1111/hpb.12199
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Identification of diagnostic and prognostic biomarkers is a research priority for the improved management of pancreatic ductal adenocarcinoma (PDAC). Insulin-like growth factor binding protein 2 (IGFBP2) and mesothelin (MSLN) have shown potential as serum biomarkers in other cancers, but have not been adequately studied in PDAC. Methods: Serum IGFBP2 and MSLN levels were quantified by enzyme-linked immunosorbent assay (ELISA) in a cohort of 84 PDAC patients, 84 healthy control subjects and 40 chronic pancreatitis (ChPT) patients. Regression models related IGFBP2 and MSLN levels to diagnosis, gender, age, stage and survival. Results: IGFPB2 and MSLN serum levels were diagnostic for PDAC in age-adjusted models (P = 0.032 and P = 0.002, respectively) when compared with ChPT and healthy control samples. At a 95% specificity threshold, the sensitivity for IGFBP2 was 22% and the sensitivity for MSLN was 17%. Neither protein approached the diagnostic accuracy of CA 19-9. However, IGFBP2 or MSLN or both correctly identified 18 of the 28 samples misidentified by CA 19-9. In age-adjusted models, neither serum IGFBP2 (P = 0.36) nor MSLN (P = 0.29) were significant predictors of survival. Discussion: Serum IGFBP2 and MSLN are weak diagnostic classifiers individually, but may be useful in a diagnostic biomarker panel.
引用
收藏
页码:670 / 676
页数:7
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