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The Real-Time Dynamic Monitoring of microRNA Function in Cholangiocarcinoma

BACKGROUND: Although many studies have confirmed a relationship between microRNAs (miRNAs) and cholangiocarcinoma (CCA), the real-time dynamics of miRNA function have not been examined. METHODS: miRNA reporter constructs were generated using a recombinant adeno-associated virus vector, which contain...

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Detalles Bibliográficos
Autores principales: Chen, Xue, Chen, Jing, Liu, Xinjuan, Guo, Zihao, Sun, Xiaoxin, Zhang, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053425/
https://www.ncbi.nlm.nih.gov/pubmed/24918778
http://dx.doi.org/10.1371/journal.pone.0099431
Descripción
Sumario:BACKGROUND: Although many studies have confirmed a relationship between microRNAs (miRNAs) and cholangiocarcinoma (CCA), the real-time dynamics of miRNA function have not been examined. METHODS: miRNA reporter constructs were generated using a recombinant adeno-associated virus vector, which contained complementary sequences for six miRNAs (miR-200a, miR-200b, miR-21, miR-146a, miR-155, and miR-221), along with two independent expression cassettes encoding the fluorescent reporter genes Fluc and Gluc. The spatio-temporal function of each miRNA was monitored both in CCA and control tissues. RESULTS: All miRNAs participated in CCA development, with distinct patterns of expression over time. The activity of miR-21 was significantly lower in female T3N0M0 CCA tissue relative to controls at three time points, yet was higher in two male T3N1M0 CCA tissues. The difference in miR-200b function between two male T3N1M0 CCA tissues and their corresponding controls peaked at 24 h, while function in a female T3N0M0 CCA was detected only at 72 h. The four remaining miRNAs (miR-200a, miR146a, miR-155, and miR-221) displayed patient-specific activity patterns in both CCA and control tissues. CONCLUSION: Significant variability was observed in the temporal function of all six miRNAs, which may play an important role in the development of CCA.