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Local and systemic inflammation: role of poly (ADP-ribose) synthetase activation by reactive nitrogen species

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Nitric Oxide and Inflammation

Abstract

Poly (ADP)-ribosyltransferase (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 emerges that under various pathophysio-logical conditions, PARS plays a crucial role in the regulation and generation of the inflammatory response. Here, we summarize the evidence favoring this new role for PARS in various forms of local and systemic inflammation and propose therapeutic opportunities afforded by PARS inhibition.

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Mabley, J. et al. (2001). Local and systemic inflammation: role of poly (ADP-ribose) synthetase activation by reactive nitrogen species. In: Salvemini, D., Billiar, T.R., Vodovotz, Y. (eds) Nitric Oxide and Inflammation. Progress in Inflammation Research. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-8241-5_5

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  • DOI: https://doi.org/10.1007/978-3-0348-8241-5_5

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