Identification of a serum biomarker signature associated with metastatic prostate cancer

被引:4
作者
Emruli, Venera Kuci [1 ,2 ]
Liljedahl, Leena [1 ,2 ]
Axelsson, Ulrika [1 ,2 ]
Richter, Corinna [1 ,2 ]
Theorin, Lisa [1 ,2 ]
Bjartell, Anders [3 ,4 ]
Lilja, Hans [4 ,5 ,6 ]
Donovan, Jenny [7 ]
Neal, David [6 ]
Hamdy, Freddie C. [6 ]
Borrebaeck, Carl A. K. [1 ,2 ]
机构
[1] Lund Univ, Dept Immunotechnol, SE-22381 Lund, Sweden
[2] Lund Univ, CREATE Hlth Translat Canc Ctr, Lund, Sweden
[3] Skane Univ Hosp, Dept Urol, Malmo, Sweden
[4] Lund Univ, Dept Translat Med, Malmo, Sweden
[5] Mem Sloan Kettering Canc Ctr, Dept Lab Med Surg & Med, 1275 York Ave, New York, NY 10021 USA
[6] Univ Oxford, Nuffield Dept Surg Sci, Oxford, England
[7] Univ Bristol, Bristol Med Sch, Bristol, Avon, England
基金
瑞典研究理事会;
关键词
affinity proteomics; antibody microarrays; biomarkers; cancer; prostate cancer; PROTEIN; INTERLEUKIN-8; EXPRESSION; MEN;
D O I
10.1002/prca.202000025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: Improved early diagnosis and determination of aggressiveness of prostate cancer (PC) is important to select suitable treatment options and to decrease over-treatment. The conventional marker is total prostate specific antigen (PSA) levels in blood, but lacks specificity and ability to accurately discriminate indolent from aggressive disease. Experimental design: In this study, we sought to identify a serum biomarker signature associated with metastatic PC. Wemeasured 157 analytes in 363 serum samples from healthy subjects, patients with non-metastatic PC and patients with metastatic PC, using a recombinant antibody microarray. Results: A signature consisting of 69 proteins differentiating metastatic PC patients from healthy controls was identified. Conclusions and clinical relevance: The clinical value of this biomarker signature requires validation in larger independent patient cohorts before providing a new prospect for detection of metastatic PC.
引用
收藏
页数:13
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