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MicroRNAs associated with the efficacy of photodynamic therapy in biliary tract cancer cell lines
AuthorWagner, Andrej ; Mayr, Christian ; Bach, Doris ; Illig, Romana ; Plätzer, Kristjan In der Gemeinsamen Normdatei der DNB nachschlagen ; Berr, Frieder ; Pichler, Martin ; Neureiter, Daniel ; Kiesslich, Tobias
Published in
International Journal of Molecular Sciences, Basel, 2014, Vol. 2014, Issue 15, page 20134-20157
PublishedMultidisciplinary Digital Publishing Institute, 2014
Document typeJournal Article
Keywords (EN)MicroRNAs / bile_duct_cancer / photodynamic_therapy / cytotoxicity / sensitivity
URNurn:nbn:at:at-ubs:3-1394 Persistent Identifier (URN)
 The work is publicly available
MicroRNAs associated with the efficacy of photodynamic therapy in biliary tract cancer cell lines [0.79 mb]
Abstract (English)

Photodynamic therapy (PDT) is a palliative treatment option for unresectable hilar biliary tract cancer (BTC) showing a considerable benefit for survival and quality of life with few side effects. Currently, factors determining the cellular response of BTC cells towards PDT are unknown. Due to their multifaceted nature, microRNAs (miRs) are a promising analyte to investigate the cellular mechanisms following PDT. For two photosensitizers, Photofrin® and Foscan®, the phototoxicity was investigated in eight BTC cell lines. Each cell line (untreated) was profiled for expression of n = 754 miRs using TaqMan® Array Human MicroRNA Cards. Statistical analysis and bioinformatic tools were used to identify miRs associated with PDT efficiency and their putative targets, respectively. Twenty miRs correlated significantly with either high or low PDT efficiency. PDT was particularly effective in cells with high levels of clustered miRs 25-93*-106b and (in case of miR-106b) a phenotype characterized by high expression of the mesenchymal marker vimentin and high proliferation (cyclinD1 and Ki67 expression). Insensitivity towards PDT was associated with high miR-200 family expression and (for miR-cluster 200a/b-429) expression of differentiation markers Ck19 and Ck8/18. Predicted and validated downstream targets indicate plausible involvement of miRs 20a*, 25, 93*, 130a, 141, 200a, 200c and 203 in response mechanisms to PDT, suggesting that targeting these miRs could improve susceptibility to PDT in insensitive cell lines. Taken together, the miRNome pattern may provide a novel tool for predicting the efficiency of PDT andfollowing appropriate functional verificationmay subsequently allow for optimization of the PDT protocol.

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