Apoptosis is central for the control and elimination of viral infections. In chronic hepatitis C virus (HCV) infection, enhanced hepatocyte apoptosis and upregulation of the death inducing ligands CD95/Fas, TRAIL and ...Apoptosis is central for the control and elimination of viral infections. In chronic hepatitis C virus (HCV) infection, enhanced hepatocyte apoptosis and upregulation of the death inducing ligands CD95/Fas, TRAIL and TNFα occur. Nevertheless, HCV infection persists in the majority of patients. The impact of apoptosis in chronic HCV infection is not well understood. It may be harmful by triggering liver fibrosis, or essential in interferon (IFN) induced HCV elimination. For virtually all HCV proteins, pro- and anti-apoptotic effects have been described, especially for the core and NS5A protein. To date, it is not known which HCV protein affects apoptosis in vivo and whether the infectious virions act pro- or anti- apoptotic. With the availability of an infectious tissue culture system, we now can address pathophysiologically relevant issues. This review focuses on the effect of HCV infection and different HCV proteins on apoptosis and of the corresponding signaling cascades.展开更多
AIM:To investigate the expression and clinical relevance of inhibitor of differentiation(ID)proteins in biliary tract cancer.METHODS:ID protein expression was analyzed in129 samples from patients with advanced biliary...AIM:To investigate the expression and clinical relevance of inhibitor of differentiation(ID)proteins in biliary tract cancer.METHODS:ID protein expression was analyzed in129 samples from patients with advanced biliary tract cancer(BTC)(45 extrahepatic,50 intrahepatic,and 34 gallbladder cancers),compared to normal controls and correlated with clinical an pathological parameters.RESULTS:ID1-3 proteins are frequently overexpressed in all BTC subtypes analyzed.No correlation between increased ID protein expression and tumor grading,tumor subtype or treatment response was detected.Survival was influenced primary tumor localization(extrahepatic vs intrahepatic and gall bladder cancer,OS 1.5 years vs 0.9 years vs 0.7 years,P=0.002),by stage at diagnosis(OS 2.7 years in stageⅠv s 0.6 years in stageⅣ,P<0.001),resection status and response to systemic chemotherapy.In a multivariate model,ID protein expression did not correlate with clinical prognosis.Nevertheless,there was a trend of shorter OS in patients with loss of cytoplasmic ID4 protein expression(P=0.076).CONCLUSION:ID protein expression is frequently deregulated in BTC but does not influence clinical prognosis.Their usefulness as prognostic biomarkers in BTC is very limited.展开更多
The COST Action FP0903 “Climate Change and Forest Mitigation and Adaptation in a Polluted Environment (MAFor)” involved 29 countries and created a platform for information exchange with experts from different fields...The COST Action FP0903 “Climate Change and Forest Mitigation and Adaptation in a Polluted Environment (MAFor)” involved 29 countries and created a platform for information exchange with experts from different fields, with the following main objectives: 1) to increase understanding of the state and potential of forest mitigation and adaptation to climate change in a polluted environment and 2) to reconcile process-oriented research, long-term monitoring and applied modelling at comprehensive forest research sites. In particular, MAFor translated the existing European knowledge on climate and air pollution dynamics into prospects for forest research and monitoring, with focus on the carbon, ozone, nitrogen and water budgets. The aim of this paper is to summarize scientific activities and achievements of MAFor: the creation of a meta-database for highlighting the available data and integrating the information from European forest research/monitoring networks;the development of a new concept of forest sites for research and monitoring (Supersites);the identification of the main knowledge gaps;and the definition of priorities for forest adaptation to climate change in a polluted environment. The action also increased European capacity building in this sector by organizing five conferences, granting 64 short-term scientific missions, organizing four training schools and publishing more than 100 papers.展开更多
文摘Apoptosis is central for the control and elimination of viral infections. In chronic hepatitis C virus (HCV) infection, enhanced hepatocyte apoptosis and upregulation of the death inducing ligands CD95/Fas, TRAIL and TNFα occur. Nevertheless, HCV infection persists in the majority of patients. The impact of apoptosis in chronic HCV infection is not well understood. It may be harmful by triggering liver fibrosis, or essential in interferon (IFN) induced HCV elimination. For virtually all HCV proteins, pro- and anti-apoptotic effects have been described, especially for the core and NS5A protein. To date, it is not known which HCV protein affects apoptosis in vivo and whether the infectious virions act pro- or anti- apoptotic. With the availability of an infectious tissue culture system, we now can address pathophysiologically relevant issues. This review focuses on the effect of HCV infection and different HCV proteins on apoptosis and of the corresponding signaling cascades.
文摘AIM:To investigate the expression and clinical relevance of inhibitor of differentiation(ID)proteins in biliary tract cancer.METHODS:ID protein expression was analyzed in129 samples from patients with advanced biliary tract cancer(BTC)(45 extrahepatic,50 intrahepatic,and 34 gallbladder cancers),compared to normal controls and correlated with clinical an pathological parameters.RESULTS:ID1-3 proteins are frequently overexpressed in all BTC subtypes analyzed.No correlation between increased ID protein expression and tumor grading,tumor subtype or treatment response was detected.Survival was influenced primary tumor localization(extrahepatic vs intrahepatic and gall bladder cancer,OS 1.5 years vs 0.9 years vs 0.7 years,P=0.002),by stage at diagnosis(OS 2.7 years in stageⅠv s 0.6 years in stageⅣ,P<0.001),resection status and response to systemic chemotherapy.In a multivariate model,ID protein expression did not correlate with clinical prognosis.Nevertheless,there was a trend of shorter OS in patients with loss of cytoplasmic ID4 protein expression(P=0.076).CONCLUSION:ID protein expression is frequently deregulated in BTC but does not influence clinical prognosis.Their usefulness as prognostic biomarkers in BTC is very limited.
基金Support by the COST Action FP0903“Climate change and forest mitigation and adaptation in the polluted environment”
文摘The COST Action FP0903 “Climate Change and Forest Mitigation and Adaptation in a Polluted Environment (MAFor)” involved 29 countries and created a platform for information exchange with experts from different fields, with the following main objectives: 1) to increase understanding of the state and potential of forest mitigation and adaptation to climate change in a polluted environment and 2) to reconcile process-oriented research, long-term monitoring and applied modelling at comprehensive forest research sites. In particular, MAFor translated the existing European knowledge on climate and air pollution dynamics into prospects for forest research and monitoring, with focus on the carbon, ozone, nitrogen and water budgets. The aim of this paper is to summarize scientific activities and achievements of MAFor: the creation of a meta-database for highlighting the available data and integrating the information from European forest research/monitoring networks;the development of a new concept of forest sites for research and monitoring (Supersites);the identification of the main knowledge gaps;and the definition of priorities for forest adaptation to climate change in a polluted environment. The action also increased European capacity building in this sector by organizing five conferences, granting 64 short-term scientific missions, organizing four training schools and publishing more than 100 papers.
