http://purl.uniprot.org/citations/20416094 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/20416094 | http://www.w3.org/2000/01/rdf-schema#comment | "BackgroundTissue fibrosis is an integral component of chronic inflammatory (liver and pancreas) diseases and pancreatic cancer. Activated pancreatic- (PSC) and hepatic-(HSC) stellate cells play a key role in fibrogenesis. To identify organ- and disease-specific stellate cell transcriptional fingerprints, we employed genome-wide transcriptional analysis of primary human PSC and HSC isolated from patients with chronic inflammation or cancer.MethodsStellate cells were isolated from patients with pancreatic ductal adenocarcinoma (n = 5), chronic pancreatitis (n = 6), liver cirrhosis (n = 5) and liver metastasis of pancreatic ductal adenocarcinoma (n = 6). Genome-wide transcriptional profiles of stellate cells were generated using our 51K human cDNA microarray platform. The identified organ- and disease specific genes were validated by quantitative RT-PCR, immunoblot, ELISA, immunocytochemistry and immunohistochemistry.ResultsExpression profiling identified 160 organ- and 89 disease-specific stellate cell transcripts. Collagen type 11a1 (COL11A1) was discovered as a novel PSC specific marker with up to 65-fold higher expression levels in PSC compared to HSC (p < 0.0001). Likewise, the expression of the cytokine CCL2 and the cell adhesion molecule VCAM1 were confined to HSC. PBX1 expression levels tend to be increased in inflammatory- vs. tumor-stellate cells. Intriguingly, tyrosine kinase JAK2 and a member of cell contact-mediated communication CELSR3 were found to be selectively up-regulated in tumor stellate cells.ConclusionsWe identified and validated HSC and PSC specific markers. Moreover, novel target genes of tumor- and inflammation associated stellate cells were discovered. Our data may be instrumental in developing new tailored organ- or disease-specific targeted therapies and stellate cell biomarkers."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.org/dc/terms/identifier | "doi:10.1186/1476-4598-9-88"xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Ansorge W."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Jiang X."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Pan Z."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Schwager C."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Weis N."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Wirkner U."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Friess H."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Abdollahi A."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Erkan M."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Kleeff J."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Giese N.A."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Debus J."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Huber P.E."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/author | "Samkharadze T."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/date | "2010"xsd:gYear |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/name | "Mol Cancer"xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/pages | "88"xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/title | "Organ-, inflammation- and cancer specific transcriptional fingerprints of pancreatic and hepatic stellate cells."xsd:string |
http://purl.uniprot.org/citations/20416094 | http://purl.uniprot.org/core/volume | "9"xsd:string |
http://purl.uniprot.org/citations/20416094 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/20416094 |
http://purl.uniprot.org/citations/20416094 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/20416094 |
http://purl.uniprot.org/uniprot/#_B4DSQ9-mappedCitation-20416094 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/20416094 |