A mouse to human search for plasma proteome changes associated with pancreatic tumor development.

Publication Type:

Journal Article


PLoS medicine, Volume 5, Issue 6, p.e123 (2008)


2008, Animals, Humans, mass spectrometry, MICE, Pancreatic Neoplasms, Proteome, PROTEOMICS, Public Health Sciences Division, RNA, Messenger, Tumor Markers, Biological


The complexity and heterogeneity of the human plasma proteome have presented significant challenges in the identification of protein changes associated with tumor development. Refined genetically engineered mouse (GEM) models of human cancer have been shown to faithfully recapitulate the molecular, biological, and clinical features of human disease. Here, we sought to exploit the merits of a well-characterized GEM model of pancreatic cancer to determine whether proteomics technologies allow identification of protein changes associated with tumor development and whether such changes are relevant to human pancreatic cancer.