Effects of angiogenic factor overexpression by human and rodent cholangiocytes in polycystic liver diseases
Luca Fabris, Massimiliano Cadamuro, Romina Fiorotto, Tania Roskams, Carlo Spirlì, Saida Melero, Aurelio Sonzogni, Ruth E. Joplin, Lajos Okolicsanyi, Mario Strazzabosco – 20 April 2006 – Liver involvement in autosomal dominant polycystic kidney disease (ADPKD) is characterized by altered remodeling of the embryonic ductal plate (DP) with presence of biliary cysts and aberrant portal vasculature. The genetic defect causing ADPKD has been identified, but mechanisms of liver cyst growth remain uncertain.