4.6 Article

Circulating Epithelial Cells in Patients with Intraductal Papillary Mucinous Neoplasm of the Pancreas

Journal

LIFE-BASEL
Volume 13, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/life13071570

Keywords

circulating epithelial cells; circulating tumor cells; intraductal papillary mucinous neoplasm; IPMN; KRAS; liquid biopsy; liquid biomarker

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Intraductal papillary mucinous neoplasm (IPMN) is a common precursor lesion of pancreatic cancer (PDAC), and its early diagnosis and treatment are crucial. The clinical management guidelines for IPMN lack satisfactory sensitivity and specificity, calling for further markers. This study isolated circulating epithelial cells (CECs) from IPMN patients, evaluated their characteristics, and compared KRAS mutations in CECs and IPMN tissue, providing additional research possibilities for understanding IPMN biology.
Intraductal papillary mucinous neoplasm (IPMN) is the most common pancreatic cyst and a precursor of pancreatic cancer (PDAC). Since PDAC has a devastatingly high mortality rate, the early diagnosis and treatment of any precursor lesion are rational. The safety of the existing guidelines on the clinical management of IPMN has been criticized due to unsatisfactory sensitivity and specificity, showing the need for further markers. Blood obtained from patients with IPMN was therefore subjected to size-based isolation of circulating epithelial cells (CECs). We isolated CECs and evaluated their cytological characteristics. Additionally, we compared Kirsten rat sarcoma viral oncogene homolog (KRAS) mutations in CECs and the primary IPMN tissue, since KRAS mutations are very typical for PDAC. Samples from 27 IPMN patients were analyzed. In 10 (37%) patients, CECs were isolated and showed a hybrid pattern of surface markers involving both epithelial and mesenchymal markers, suggesting a possible EMT process of the cells. Especially, patients with high-grade dysplasia in the main specimen were all CEC-positive. KRAS mutations were also present in CECs but less common than in IPMN tissue. The existence of CEC in IPMN patients offers additional blood-based research possibilities for IMPN biology.

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