Büro PER 17 - 123
+41 26 300 9409
Csaba Szabo has joined the University of Fribourg in 2018. The research interest of Pr. Szabo and his group focuses on the biological and pathophysiological roles of various labile, diffusible small biological molecules.
One class of these molecules is called free radicals. These species (for example superoxide, or nitric oxide) are produced in various cells during biological and pathophysiological processes and are involved in various processes ranging from cell death to inflammatory responses. Free radicals can induce cellular injury through damage to proteins, lipids or nucleic acids. One of the consequences of free radical mediated cellular injury involves the activation of an enzyme called poly(ADP-ribose) polymerase (PARP). Pr. Szabo has been working on the role of PARP in various pathophysiological processes (vascular injury, circulatory shock, inflammation) for many years, and is now involved in efforts seeking to repurpose clinically used (for cancer) PARP inhibitors for the experimental therapy of various non-oncological diseases.
Nitric oxide (NO), carbon monoxide (CO), and hydrogen sulfide (H2S) represent a unique class of labile biological mediators called gasotransmitters. These molecules travel easily through cell membranes and mediate multiple processes in the vascular, immune and nervous system through acting on multiple interrelated receptors and effectors. For the last decade, Pr. Szabo has been active in the field of H2S biology, where he studies the pathophysiology, pharmacology and experimental therapy of various diseases (vascular, metabolic, cancer) in the context of alterations in H2S homeostasis.
3-mercaptopyruvate sulfurtransferase (3-MST) is one of the enzymes involved in the production of H2S. This enzyme, present in the mitochondria as well as in the cytosol, is involved in the regulation of bioenergetic and signaling processes. With the support of a Swiss National Foundation (SNF) grant, Pr. Szabo's group studies the involvement of the 3-MST system in the regulation of hepatocyte dysfunction, adipocyte differentiation and vascular dysfunction in the context of metabolic disease.
C. Szabo, T. Panagaki, F. Augsburger, N.Duffey
3-mercaptopyruvate sulfurtransferase (3-MST) and the H2S produced from it is also involved in the support of metabolic and signaling functions of cancer cells. With the support of a Novartis Foundation grant, Pr. Szabo's group studies the involvement of the 3-MST system in the regulation of colon cancer cell growth and differentiation.
C. Szabo, E. Randi, F. Augsburger, N. Duffey
CBS is one of the enzymes involved in the production of H2S. This enzyme is overexpressed in Down Syndrome and, according to the so-called "Kamoun Hypothesis", it produces excessive amounts of H2S that may lead to cytotoxicity. With the support of a LeJenue Foundation (Paris) grant, Pr. Szabo's group studies the involvement of the CBS system in the regulation of mitochondrial function, cell proliferation and cell viability in cell-based models of Down Syndrome.
C. Szabo, T. Panagaki, E. Randi, F. Augsburger, N. Duffey
The key enzyme responsible for H2S production in colon cancer cells is cystathionine beta synthase (CBS). Although the phenomenon itself that cancer cells produce increased amounts of H2S to support their various biological functions is now well accepted, there are still significant gaps in our knowledge, with respect tothe mechanism(s) how CBS is upregulated and activated in colon cancer cells in the early stages of colonic polypogenesis/carcinogenesis. With the support of a Swiss Krebsliga grant,identification of these activation and upregulation mechanisms is the goal of the current project.
C. Szabo, E. Randi, T. Panagaki, F. Augsburger, N. Duffey