[10] However, in contrast to our study, where ICC was exclusively detectable, some tumors in this germline model were identified as hepatocellular carcinoma (HCC) or showed a mixed phenotype. These differences may be explainable by the fact that we transformed adult cells, whereas the albumin-Cre-mediated KRas/p53-induced ICC is initially activated in liver progenitors during late

embryogenesis. Outgrowth of metastases and disease recurrence is life-limiting in ICC patients after surgical resection of the tumor. In our model, we PD0325901 supplier could not detect any manifest metastasis when the primary tumor was not removed by resection. However, primary tumor formation was frequently accompanied by formation of satellites and vascular invasion, this website which can be interpreted as a premetastatic stage. Because of single tumor formation, we could use this model to investigate the pattern of tumor recurrence after curative R0-resection and the impact of adjuvant systemic therapy in ICC. After surgical resection of the primary tumor, we observed a clear correlation between survival outcomes and tumor stages at the time of surgery,

which were classified by tumor size and histopathologic grading. While R0-resection was curative in early ICC, we observed a high incidence of local recurrence/intrahepatic metastases, peritoneal carcinomatosis, and frequent manifestation of lung metastases in advanced ICC. These findings reflect the clinical situation in humans, where the liver is the most common site of recurrence after resection of the primary tumor in ICC patients.[19] Therefore, adjuvant systemic therapy is the favorable treatment of biliary tract cancers.[22] With adjuvant gemcitabine chemotherapy we could show a significantly improved survival of animals after R0-resection. In contrast to the ineffective palliative gemcitabine treatment in our model, our results strongly recommend adjuvant gemcitabine chemotherapy for advanced ICC. We established for the first time a murine tumor R0-resection model of

an autochthonously developed selleck screening library ICC. Our animal model overcomes several important drawbacks of germline genetically engineered mouse models. Therefore, it holds great promise for preclinical evaluation of novel targeted therapies. Most important, this model facilitates investigations of how tumor genetics influence the outcome of adjuvant and neoadjuvant therapies. In addition, it appears likely that the locoregional electroporation method of oncogenic transposons can be easily adapted to genetic and morphologic modeling of further tumor entities to allow for predictive preclinical studies. Additional Supporting Information may be found in the online version of this article. “
“Advanced glycation end products (AGEs) are nonenzymatic modifications of proteins by reducing sugars.