RT Journal Article
T1 Role of p63 and p73 isoforms on the cell death in patients with hepatocellular carcinoma submitted to orthotopic liver transplantation.
A1 Gonzalez, Raul
A1 De la Rosa, Angel J
A1 Rufini, Alessandro
A1 Rodriguez-Hernandez, Maria A
A1 Navarro-Villaran, Elena
A1 Marchal, Trinidad
A1 Pereira, Sheila
A1 De la Mata, Manuel
A1 Müller-Schilling, Martina
A1 Pascasio-Acevedo, Juan M
A1 Ferrer-Rios, Maria T
A1 Gomez-Bravo, Miguel A
A1 Padillo, Francisco J
A1 Muntane, Jordi
K1 Protein Isoforms
K1 Receptors, Death Domain
K1 Transcription Factors
K1 Tumor Protein p73
K1 Tumor Suppressor Proteins
AB Patients with hepatocellular carcinoma (HCC) submitted to orthotopic liver transplantation (OLT) have a variable 5-year survival rate limited mostly by tumor recurrence. The etiology, age, sex, alcohol, Child-Pugh, and the immunesuppressor have been associated with tumour recurrence. The expression of ΔNp73 is related to the reduced survival of patients with HCC. The study evaluated the expression of p63 and p73 isoforms and cell death receptors, and their relation to tumour recurrence and survival. The results were in vitro validated in HCC cell lines. HCC sections from patients submitted to OLT were used. The in vitro study was done in differentiated hepatitis B virus (HBV)-expressing Hep3B and control HepG2 cells. The expression of cell death receptors and cFLIPS/L, caspase-8 and -3 activities, and cell proliferation were determined in control and p63 and p73 overexpressing HCC cells. The reduced tumor expression of cell death receptors and TAp63 and TAp73, and increased ΔNp63 and ΔNp73 expression were associated with tumor recurrence and reduced survival. The in vitro study demonstrated that HBV-expressing Hep3B vs HepG2 cells showed reduced expression of p63 and p73, cell death receptors and caspase activation, and increased cFLIPL/cFLIPS ratio. The overexpression of TAp63 and TAp73 exerted a more potent pro-apoptotic and anti-proliferative effects in Hep3B than HepG2-transfected cells which was related to cFLIPL upregulation. The reduction of TAp63 and TAp73 isoforms, rather than alteration of ΔN isoform expression, exerted a significant functional repercussion on cell death and proliferation in HBV-expressing HepB cells.
PB Public Library of Science
YR 2017
FD 2017-03-07
LK http://hdl.handle.net/10668/11017
UL http://hdl.handle.net/10668/11017
LA en
NO González R, De la Rosa ÁJ, Rufini A, Rodríguez-Hernández MA, Navarro-Villarán E, Marchal T, et al. Role of p63 and p73 isoforms on the cell death in patients with hepatocellular carcinoma submitted to orthotopic liver transplantation. PLoS One. 2017 Mar 28;12(3):e0174326
DS RISalud
RD Apr 5, 2025