Omics approaches in pancreatic adenocarcinoma

Pancreatic ductal adenocarcinoma, which represents 80% of pancreatic cancers, is mainly diagnosed when treatment with curative intent is not possible. Consequently, the overall five-year survival rate is extremely dismal—around 5% to 7%. In addition, pancreatic cancer is expected to become the secon...

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Autores: Gonzalez, I. (Iranzu)|||/items/3f93de11-acd3-433e-9279-8db524437940, Viudez, A. (Antonio)|||/items/cdc323b7-efce-4d1e-97d9-713f0789385e, Goñi, S. (Saioa)|||/items/30c9118a-59e0-41e1-9d9a-a41414437869, Santamaria, E. (Enrique)|||/items/fc2c70d6-973c-4d67-8185-6c56a59477c8, García, E. (Estefania)|||/items/fca809cd-48b9-4cad-8565-91c5005ab9a5, Pérez-Sanz, J. (Jairo)|||/items/d49390a5-8bf3-4e7c-9506-3bba02d75222, Hernández-García, I. (Irene)|||/items/18b84293-3843-405a-a1c4-a333668a43ad, Sala-Elarre, P. (Pablo)|||/items/a91400e6-6375-4f58-a68e-9adf0eb4d678, Arrazubi, V. (Virginia)|||/items/60bcb6dd-f509-44a5-8670-4473b720786c, Oyaga-Iriarte, E. (Esther)|||/items/b28302c2-44c9-4863-8641-b9188b664911, Zarate, R. (Ruth)|||/items/08593a15-ef00-4db2-bf43-3e6e4c3d5161, Arévalo, S. (Sara)|||/items/661f870b-9efc-47c5-a935-47c51f4964c8, Sayar, O. (Onintza)|||/items/1780ca24-71aa-4a05-ada2-296c83338651, Vera, R. (Ruth)|||/items/c5e822da-e29b-4f65-bb1c-be8bb5b999e1, Fernandez-Irigoyen, J. (Joaquín)|||/items/700f4366-d68f-4161-af03-2cac47ea718d
Tipo de recurso: artículo
Fecha de publicación:2019
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/62533
Acceso en línea:https://hdl.handle.net/10171/62533
Access Level:acceso abierto
Palabra clave:Pancreatic adenocarcinoma
ctDNA
Proteomic
Genomic
Metabolomic
Lipidomic
FFPE
Tissue
Body fluids
Descripción
Sumario:Pancreatic ductal adenocarcinoma, which represents 80% of pancreatic cancers, is mainly diagnosed when treatment with curative intent is not possible. Consequently, the overall five-year survival rate is extremely dismal—around 5% to 7%. In addition, pancreatic cancer is expected to become the second leading cause of cancer-related death by 2030. Therefore, advances in screening, prevention and treatment are urgently needed. Fortunately, a wide range of approaches could help shed light in this area. Beyond the use of cytological or histological samples focusing in diagnosis, a plethora of new approaches are currently being used for a deeper characterization of pancreatic ductal adenocarcinoma, including genetic, epigenetic, and/or proteo-transcriptomic techniques. Accordingly, the development of new analytical technologies using body fluids (blood, bile, urine, etc.) to analyze tumor derived molecules has become a priority in pancreatic ductal adenocarcinoma due to the hard accessibility to tumor samples. These types of technologies will lead us to improve the outcome of pancreatic ductal adenocarcinoma patients.