Abstract
We recently demonstrated that a novel storage and transport mechanism for nitric oxide (NO) mediated by glutathione-S-transferase P1 (GSTP1) and multidrug resistance protein 1 (MRP1/ABCC1), protects M1-macrophage (M1-MØ) models from large quantities of endogenous NO. This system stores and transports NO as dinitrosyl-dithiol-iron complexes (DNICs) composed of iron, NO and glutathione (GSH). Hence, this gas with contrasting anti- and pro-tumor effects, which has been assumed to be freely diffusible, is a tightly-regulated species in M1-MØs. These control systems prevent NO cytotoxicity and may be responsible for delivering cytotoxic NO as DNICs via MRP1 from M1-MØs, to tumor cell targets.
Originalsprog | Engelsk |
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Tidsskrift | B B A - Reviews on Cancer |
Vol/bind | 1861 |
Udgave nummer | 5 Pt A |
Sider (fra-til) | 995-999 |
Antal sider | 5 |
ISSN | 0006-3002 |
DOI | |
Status | Udgivet - maj 2017 |