Detalle Publicación

A novel serum metabolomic profile for the differential diagnosis of distal cholangiocarcinoma and pancreatic ductal adenocarcinoma

Autores: Macias, R. I. R. (Autor de correspondencia); Munoz-Bellvis, L. ; Sanchez-Martin, A. ; Arretxe, E. ; Martinez-Arranz, I. ; Lapitz, A.; Gutierrez, M. L. ; La Casta, A.; Alonso, C.; Gonzalez, L. M.; Ávila Zaragoza, Matías Antonio; Martinez-Chantar, M. L.; Castro, R. E.; Bujanda, L. ; Banales, J. M. ; Marin, J. J. G.
Título de la revista: CANCERS
ISSN: 2072-6694
Volumen: 12
Número: 6
Páginas: 1433
Fecha de publicación: 2020
The diagnosis of adenocarcinomas located in the pancreas head, i.e., distal cholangiocarcinoma (dCCA) and pancreatic ductal adenocarcinoma (PDAC), constitutes a clinical challenge because they share many symptoms, are not easily distinguishable using imaging techniques and accurate biomarkers are not available. Searching for biomarkers with potential usefulness in the differential diagnosis of these tumors, we have determined serum metabolomic profiles in healthy controls and patients with dCCA, PDAC or benign pancreatic diseases (BPD). Ultra-high-performance liquid chromatography coupled to mass spectrometry (UHPLC-MS) analysis was performed in serum samples from dCCA (n= 34), PDAC (n= 38), BPD (n= 42) and control (n= 25) individuals, divided into discovery and validation cohorts. This approach permitted 484 metabolites to be determined, mainly lipids and amino acids. The analysis of the results led to the proposal of a logistic regression model able to discriminate patients with dCCA and PDAC (AUC value of 0.888) based on the combination of serum levels of nine metabolites (acylcarnitine AC(16:0), ceramide Cer(d18:1/24:0), phosphatidylcholines PC(20:0/0:0) and PC(O-16:0/20:3), lysophosphatidylcholines PC(20:0/0:0) and PC(0:0/20:0), lysophosphatidylethanolamine PE(P-18:2/0:0), and sphingomyelins SM(d18:2/22:0) and SM(d18:2/23:0)) and CA 19-9. In conclusion, we propose a novel specific panel of serum metabolites that can help in the differential diagnosis of dCCA and PDAC. Further validation of their clinical usefulness in prospective studies is required.