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Protein expression of ABCC2 and SLC22A3 associates with prognosis of pancreatic adenocarcinoma
L. Cervenkova, O. Vycital, J. Bruha, J. Rosendorf, R. Palek, V. Liska, O. Daum, B. Mohelnikova-Duchonova, P. Soucek,
Language English Country Great Britain
Document type Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't
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- MeSH
- Adenocarcinoma * metabolism mortality pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Survival Rate MeSH
- Neoplasm Proteins biosynthesis MeSH
- Pancreatic Neoplasms * metabolism mortality pathology MeSH
- Disease-Free Survival MeSH
- Organic Cation Transport Proteins biosynthesis MeSH
- Multidrug Resistance-Associated Proteins biosynthesis MeSH
- Gene Expression Regulation, Neoplastic * MeSH
- Aged MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
ATP-binding cassette (ABC) and solute carrier (SLC) transporters translocate diverse substances across cellular membranes and their deregulation may cause drug resistance of cancers. This study investigated significance of protein expression and cellular localization of the previously suggested putative prognostic markers ABCC2 and SLC22A3 in pancreatic cancer patients. Protein localization and brush border staining intensity of ABCC2 and SLC22A3 was assessed in tumor tissue blocks of 65 pancreatic cancer patients and associated with clinical data and survival of patients with regard to therapy. Negative SLC22A3 brush border staining in pancreatic tumors significantly increased the risk of both disease progression and patient´s death in univariate analyses. Multivariate analyses confirmed the association of SLC22A3 expression with progression-free survival of patients. A subgroup analysis of patients treated with regimens based on nucleoside analogs suggested that patients with negative brush border staining or apical localization of SLC22A3 in tumor cells have worse overall survival. The combination of positive ABCC2 and negative SLC22A3 brush border staining predicted worst overall survival and patients with positive brush border staining of both proteins had best overall and progression-free survival. The present study shows for the first time that the protein presence and to some extent also localization of SLC22A3 significantly associate with prognosis of pancreatic cancer in both unstratified and chemotherapy-treated patients. The combination of ABCC2 and SLC22A3 brush border staining also needs further attention in this regard.
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