| Literature DB >> 17192050 |
H J Zeh1, S Winikoff, D P Landsittel, E Gorelik, A M Marrangoni, L Velikokhatnaya, M T Winans, K Lee, A Moser, D Bartlett, M T Lotze, J M Siegfried, D Whitcomb, G Papacristou, A Slivka, W L Bigbee, A E Lokshin.
Abstract
Early detection of pancreatic cancer might improve clinical outcome. Significant alterations in the levels of individual serum cytokines have been reported in pancreatic cancer. We hypothesized that a multicytokine panel could serve as biomarkers for pancreatic cancer. To evaluate the diagnostic utility of such a panel, we have utilized a novel multianalyte LabMAP profiling technology that allows simultaneous measurement of multiple markers. In this study, a panel of 31 serological markers including cytokines, chemokines, growth and angiogenic factors in combination with CA 19-9 was analyzed in sera of pancreatic cancer patients, patients with chronic pancreatitis, and matched control healthy subjects. Statistical analysis identified a multicytokine panel that was able to distinguish pancreatic cancer from healthy controls with a sensitivity of 85.7% and specificity of 92.3%, which was superior to performance of CA 19-9 alone. Importantly, a multicytokine panel allowed the discrimination of pancreatic cancer from chronic pancreatitis with high sensitivity of 98% and specificity of 96.4%. In conclusion, we demonstrated that analysis of multiple serum cytokines using a novel LabMAP technology is a promising approach for development of a diagnostic assay for pancreatic cancer.Entities:
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Year: 2005 PMID: 17192050 DOI: 10.3233/cbm-2005-1601
Source DB: PubMed Journal: Cancer Biomark ISSN: 1574-0153 Impact factor: 4.388