Abstract
Poly (ADP-ribose) synthetase (PARS), also known as poly(ADP-ribose) polymerase (PARP), is an abundant nuclear enzyme present throughout the phylogenetic spectrum [1]. The precise physiologic roles of PARS remain undefined; its traditional role as a DNA-repair enzyme has been questioned by recent studies [2]. PARS appears to play diverse roles, participating in DNA repair [3,4], chromatin relaxation [5], cell differentiation [6], DNA replication [7], transcriptional regulation [8], control of cell cycle [9], p53 expression and apoptosis [10], and transformation [11]. In the last decade, the novel concept has emerged that in circulatory shock, and various other pathophysiological conditions, PARS plays a crucial role in the regulation and generation of the inflammatory response and cell and organ injury. Here we summarize the evidence favoring this new role for PARS in circulatory shock and evaluate the therapeutic opportunities afforded by PARS inhibition.
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Liaudet, L., Soriano, F.G., Szabó, C. (2001). Poly (ADP-Ribose) Synthetase as a Novel Therapeutic Target for Circulatory Shock. In: Vincent, JL. (eds) Yearbook of Intensive Care and Emergency Medicine 2001. Yearbook of Intensive Care and Emergency Medicine 2001, vol 2001. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-59467-0_8
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DOI: https://doi.org/10.1007/978-3-642-59467-0_8
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