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Omics Approaches in Pancreatic Adenocarcinoma.
González-Borja, Iranzu; Viúdez, Antonio; Goñi, Saioa; Santamaria, Enrique; Carrasco-García, Estefania; Pérez-Sanz, Jairo; Hernández-García, Irene; Sala-Elarre, Pablo; Arrazubi, Virginia; Oyaga-Iriarte, Esther; Zárate, Ruth; Arévalo, Sara; Sayar, Onintza; Vera, Ruth; Fernández-Irigoyen, Joaquin.
Affiliation
  • González-Borja I; OncobionaTras Lab, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA) Irunlarrea 3, 31008 Pamplona, Spain.
  • Viúdez A; OncobionaTras Lab, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA) Irunlarrea 3, 31008 Pamplona, Spain. aviudezb@navarra.es.
  • Goñi S; Medical Oncology Department, Complejo Hospitalario de Navarra, Irunlarrea 3, 31008 Pamplona, Spain. aviudezb@navarra.es.
  • Santamaria E; OncobionaTras Lab, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA) Irunlarrea 3, 31008 Pamplona, Spain.
  • Carrasco-García E; Clinical Neuroproteomics Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), Irunlarrea 3, 31008 Pamplona, Spain.
  • Pérez-Sanz J; Proteored-ISCIII, Proteomics Unit, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA), Irunlarrea 3, 31008 Pamplona, Spain.
  • Hernández-García I; Instituto de Investigación Sanitaria de Navarra (IdiSNA), Irunlarrea 3, 31008 Pamplona, Spain.
  • Sala-Elarre P; Grupo de Oncología Celular, Instituto de Investigación Sanitaria Biodonostia, 20014 San Sebastián, Spain.
  • Arrazubi V; CIBER de Fragilidad y Envejecimiento Saludable (CIBERfes), 28029 Madrid, Spain.
  • Oyaga-Iriarte E; OncobionaTras Lab, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA) Irunlarrea 3, 31008 Pamplona, Spain.
  • Zárate R; Medical Oncology Department, Complejo Hospitalario de Navarra, Irunlarrea 3, 31008 Pamplona, Spain.
  • Arévalo S; Medical Oncology Department, Clínica Universidad de Navarra, 31008 Pamplona, Spain.
  • Sayar O; Medical Oncology Department, Complejo Hospitalario de Navarra, Irunlarrea 3, 31008 Pamplona, Spain.
  • Vera R; Pharmamodelling S.L., 31008 Pamplona, Spain.
  • Fernández-Irigoyen J; OncobionaTras Lab, Navarrabiomed, Complejo Hospitalario de Navarra (CHN), Universidad Pública de Navarra (UPNA) Irunlarrea 3, 31008 Pamplona, Spain.
Cancers (Basel) ; 11(8)2019 07 25.
Article in En | MEDLINE | ID: mdl-31349663
ABSTRACT
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancers (Basel) Year: 2019 Document type: Article Affiliation country: España

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cancers (Basel) Year: 2019 Document type: Article Affiliation country: España