TY - JOUR
T1 - Cholangiocyte injury and ductopenic syndromes
AU - Xia, Xuefeng
AU - DeMorrow, Sharon
AU - Francis, Heather
AU - Glaser, Shannon
AU - Alpini, Gianfranco
AU - Marzioni, Marco
AU - Fava, Giammarco
AU - LeSage, Gene
PY - 2007/11
Y1 - 2007/11
N2 - Cholangiopathies are characterized by a predominately bile duct-directed inflammatory response that leads to bile duct injury and, if the injury is persistent, bile duct loss and the chance of developing bile duct cancer (cholangiocarcinoma). Although the cholangiopathies have broad range of etiologies and pathogenesis (e.g., inherited disorders, autoimmune disorders, infections, drug-induced, ischemia, and unknown etiology), all share the common pathogenetic target - the biliary epithelial cell (cholangiocyte). For the most part, the pathogenesis of these diseases is poorly understood, which correspondingly has restricted clinicians to nonspecific and usually ineffective therapies for these disorders. Nevertheless, significant advances toward the understanding of the mechanisms involved in cholangiocyte-directed inflammation, biliary fibrosis, cholangiocyte death, and cholangiocarcinoma have unfolded over the past 15 years that may provide us new hopes and schemes for treatment of these disorders.
AB - Cholangiopathies are characterized by a predominately bile duct-directed inflammatory response that leads to bile duct injury and, if the injury is persistent, bile duct loss and the chance of developing bile duct cancer (cholangiocarcinoma). Although the cholangiopathies have broad range of etiologies and pathogenesis (e.g., inherited disorders, autoimmune disorders, infections, drug-induced, ischemia, and unknown etiology), all share the common pathogenetic target - the biliary epithelial cell (cholangiocyte). For the most part, the pathogenesis of these diseases is poorly understood, which correspondingly has restricted clinicians to nonspecific and usually ineffective therapies for these disorders. Nevertheless, significant advances toward the understanding of the mechanisms involved in cholangiocyte-directed inflammation, biliary fibrosis, cholangiocyte death, and cholangiocarcinoma have unfolded over the past 15 years that may provide us new hopes and schemes for treatment of these disorders.
KW - Bile duct epithelium
KW - Cholangiopathy
KW - Ductopenia
KW - Primary biliary cirrhosis
KW - Primary sclerosing cholangitis
UR - http://www.scopus.com/inward/record.url?scp=35948937304&partnerID=8YFLogxK
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U2 - 10.1055/s-2007-991516
DO - 10.1055/s-2007-991516
M3 - Article
C2 - 17979076
AN - SCOPUS:35948937304
VL - 27
SP - 401
EP - 412
JO - Seminars in Liver Disease
JF - Seminars in Liver Disease
SN - 0272-8087
IS - 4
ER -