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siRNA Delivery for Control of Cyclin D1 and E2F1 Expression in Crohn’s Disease

Evidence in inflammatory bowel diseases (IBD) supports a connection between inflammation and cancer due to the alteration of the cell cycle with loss of control at the G1/S checkpoint. In this study, we analyze the expression and modulation of CyD1 and E2F1 in colon explants from Crohn’s disease (CD...

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Detalles Bibliográficos
Autores principales: Russo, Ilaria, Carrizzo, Albino, Bochicchio, Sabrina, Piazza, Ornella, Lamberti, Gaetano, Barba, Anna Angela, Vecchione, Carmine, Zeppa, Pio, Iovino, Paola, Bucci, Cristina, Santonicola, Antonella, Ciacci, Carolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Università di Salerno 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056255/
https://www.ncbi.nlm.nih.gov/pubmed/30050877
Descripción
Sumario:Evidence in inflammatory bowel diseases (IBD) supports a connection between inflammation and cancer due to the alteration of the cell cycle with loss of control at the G1/S checkpoint. In this study, we analyze the expression and modulation of CyD1 and E2F1 in colon explants from Crohn’s disease (CD) patients. We used ex vivo culture of colon explants from 4 CD patients and 2 healthy controls, stimulated with lipopolysaccharide from Escherichia Coli (EC-LPS). Commercial siRNAs for CyD1 and E2F1 inhibition were encapsulated in Invivofectamine® and in purposely produced nanoliposomal vectors to silencing CyD1 and E2F1 expression. Western blot analysis was used to investigate the effect of siRNA on CyD1, E2F1 and cyclooxygenase 2 (COX-2) expression. In CD patients colon explants, CyD1 and E2F1 increased after the inflammatory stimulus but siRNA silencing attenuated their expression and controlled the COX-2 expression too. These data represent a prelimiary exploration of in vitro siRNA use.