PMID- 12161009 OWN - NLM STAT- MEDLINE DCOM- 20030613 LR - 20190813 IS - 0303-7207 (Print) IS - 0303-7207 (Linking) VI - 193 IP - 1-2 DP - 2002 Jul 31 TI - Alfa and beta estrogen receptors and the biliary tree. PG - 105-8 AB - This manuscript summarizes recent data showing that estrogens and their receptors play an important role in modulating cholangiocyte proliferation. We have recently demonstrated that rat cholangiocytes express both estrogen receptors (ER)-alpha and -beta subtypes, while hepatocytes only express ER-alpha. ER and especially the ER-beta subtype, are overexpressed in cholangiocytes proliferating after bile duct ligation (BDL) in the rat, in association with enlarged bile duct mass and with enhanced estradiol serum levels. Cholangiocyte proliferation, during BDL, is impaired by estrogen antagonists (tamoxifen, ICI 182,780) which furthermore, induce the overexpression of Fas antigen and activate apoptosis of proliferating cholangiocytes. 17beta-estradiol stimulates, in vitro cholangiocyte proliferation, and this effect is individually blocked by tamoxifen or ICI 182,780. Cholangiocyte proliferation during BDL was associated with an enhanced protein expression of phosphorylated extracellular regulated kinases (ERK)1/2 which is, in contrast, negatively modulated by tamoxifen in association with its antiproliferative effect. This indicates a major involvement of the ERK system in the estrogen modulation of cholangiocyte proliferation. CI - Copyright 2002 Elsevier Science Ireland Ltd. FAU - Alvaro, Domenico AU - Alvaro D AD - Division of Gastroenterology, Department of Clinical Medicine, University of Rome 'La Sapienza', Via valsolda 45/i, 00141 Rome, Italy. alvaro@axrma.uniromal.it FAU - Alpini, G AU - Alpini G FAU - Onori, P AU - Onori P FAU - Franchitto, A AU - Franchitto A FAU - Glaser, S S AU - Glaser SS FAU - Le Sage, G AU - Le Sage G FAU - Folli, F AU - Folli F FAU - Attili, A F AU - Attili AF FAU - Gaudio, E AU - Gaudio E LA - eng GR - DK58411/DK/NIDDK NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. PT - Research Support, U.S. Gov't, P.H.S. PT - Review PL - Ireland TA - Mol Cell Endocrinol JT - Molecular and cellular endocrinology JID - 7500844 RN - 0 (Estrogen Receptor alpha) RN - 0 (Estrogen Receptor beta) RN - 0 (Receptors, Estrogen) SB - IM MH - Animals MH - Bile Ducts, Intrahepatic/chemistry/*cytology MH - Cell Division/drug effects MH - Estrogen Receptor alpha MH - Estrogen Receptor beta MH - Humans MH - Rats MH - Receptors, Estrogen/*metabolism MH - Signal Transduction RF - 23 EDAT- 2002/08/06 10:00 MHDA- 2003/06/14 05:00 CRDT- 2002/08/06 10:00 PHST- 2002/08/06 10:00 [pubmed] PHST- 2003/06/14 05:00 [medline] PHST- 2002/08/06 10:00 [entrez] AID - S030372070200103X [pii] AID - 10.1016/s0303-7207(02)00103-x [doi] PST - ppublish SO - Mol Cell Endocrinol. 2002 Jul 31;193(1-2):105-8. doi: 10.1016/s0303-7207(02)00103-x.