| Literature DB >> 24333829 |
Andrew D Rhim1, Fredrik I Thege2, Steven M Santana3, Timothy B Lannin3, Trisha N Saha4, Shannon Tsai5, Lara R Maggs5, Michael L Kochman6, Gregory G Ginsberg6, John G Lieb5, Vinay Chandrasekhara5, Jeffrey A Drebin7, Nuzhat Ahmad8, Yu-Xiao Yang8, Brian J Kirby9, Ben Z Stanger10.
Abstract
Hematogenous dissemination is thought to be a late event in cancer progression. We recently showed in a genetic model of pancreatic ductal adenocarcinoma that pancreas cells can be detected in the bloodstream before tumor formation. To confirm these findings in humans, we used microfluidic geometrically enhanced differential immunocapture to detect circulating pancreas epithelial cells in patient blood samples. We captured more than 3 circulating pancreas epithelial cells/mL in 7 of 21 (33%) patients with cystic lesions and no clinical diagnosis of cancer (Sendai criteria negative), 8 of 11 (73%) with pancreatic ductal adenocarcinoma, and in 0 of 19 patients without cysts or cancer (controls). These findings indicate that cancer cells are present in the circulation of patients before tumors are detected, which might be used in risk assessment.Entities:
Keywords: Circulating Tumor Cells; Early Detection; IPMN; Pancreatic Cancer
Mesh:
Year: 2013 PMID: 24333829 PMCID: PMC4514438 DOI: 10.1053/j.gastro.2013.12.007
Source DB: PubMed Journal: Gastroenterology ISSN: 0016-5085 Impact factor: 22.682