Cell Proliferation · 2020 · 46 citations · 37 references
MedicineOncologyPathologyMolecular DiagnosticsMolecular OncologyMolecular PathologyCancer BiomarkersCancer DetectionCancer DiagnosisCancer Molecular DiagnosticsPancreatic CancerTumor MarkersBiomarker DetectionCancer DiagnosticsCirculating Tumor BiomarkersCirculating Tumor Cell BiomarkersCirculating Tumor Cell MonitoringCirculating Tumor MarkersNovel Circulating BiomarkersPancreatic Cancer Detection
Abstract Objectives To detect folate receptor (FR)‐positive circulating tumour cells (FR + CTCs) by using ligand‐targeted polymerase chain reaction (LT‐PCR) in periampullary cancer patients and to investigate the diagnostic value of FR + CTCs in distinguishing pancreatic cancer (PC) from benign pancreatic disease. Materials and Methods CTCs were enriched from 3 mL of peripheral blood and portal vein blood by immunomagnetic depletion of leucocytes and were then detected by LT‐PCR. The diagnostic performance of FR + CTCs in PC was investigated by receiver‐operating characteristic curve analysis. Results In total, 57 consecutive patients, including 46 patients with PC, five patients with non‐pancreatic periampullary cancer (non‐PC) and six patients with benign pancreatic diseases, were enrolled. FR + CTC levels were significantly higher in patients with malignant diseases (PC and non‐PC) than in patients with benign pancreatic diseases ( P < .01). There was no notable difference in CTC levels between patients with PC and those with non‐PC ( P > .05). The combination of FR + CTCs with carbohydrate antigen 19‐9 (CA19‐9) had better diagnostic efficiency than each of these two markers alone, with high sensitivity (97.8%) and specificity (83.3%). Conclusions LT‐PCR is feasible and reliable for detecting FR + CTCs in patients with periampullary cancer. FR + CTCs, especially when used in combination with CA19‐9, have potential as a biomarker for the diagnosis of PC.
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Andrew D. Rhim, Emily T. Mirek, Nicole M. Aiello et al. · Cell · 2012 · 2.1K citations · Full text
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