Data from Extracellular ATP and Purinergic P2Y<sub>2</sub> Receptor Signaling Promote Liver Tumorigenesis in Mice by Exacerbating DNA Damage

Abstract

<div>Abstract<p>Release of ATP to the extracellular compartment and subsequent activation of purinergic receptors is a conserved mechanism mediating inflammatory responses and cell fate decisions in various organs including the liver. Previous findings suggest that extracellular ATP may promote liver tumorigenesis, however, the underlying mechanisms are poorly understood. Therefore, our aim was to dissect the functions of extracellular ATP and P2Y<sub>2</sub> receptors (P2Y<sub>2</sub>R) during hepatocarcinogenesis. Liver tumors were induced in wild-type and <i>P2y<sub>2</sub>r</i><sup>−/−</sup> knockout mice by intraperitoneal diethylnitrosamine (DEN) injection. Tumorigenesis was analyzed after 8 to 10 months and molecular analyses were performed at different stages of tumorigenesis <i>in vivo</i>, as well as in primary mouse hepatocytes <i>in vitro</i>. Liver tumor incidence and tumor numbers were strongly reduced in <i>P2y<sub>2</sub>r</i><sup>−/−</sup> mice, whereas tumor size and morphology were comparable to wild-type controls, suggesting that P2Y<sub>2</sub>R contributes to tumor initiation. Mechanistically, hepatocyte proliferation in DEN-treated <i>P2y<sub>2</sub>r</i><sup>−/−</sup> mice was reduced, which correlated with reduced c-JUN and CCND1 but increased p21 expression. Moreover, DNA damage as determined by hepatocellular expression of γH2A.X and of genes related to genotoxic stress, as well as STAT3 phosphorylation, was reduced in the absence of <i>P2y<sub>2</sub>r</i>. Administration of genotoxic agents to primary hepatocytes <i>in vitro</i> confirmed that DNA damage was indeed exacerbated by extracellular ATP, subsequent P2Y<sub>2</sub>R activation, and downstream intracellular calcium-dependent signal transduction. In conclusion, our data reveal that extracellular ATP and subsequent P2Y<sub>2</sub>R function stimulate DNA damage responses and hepatocyte proliferation, thereby promoting hepatocarcinogenesis. Targeting this pathway may be an attractive approach for chemoprevention of hepatocellular carcinoma.</p>Significance:<p>Extracellular ATP and subsequent P2Y<sub>2</sub> receptor function stimulate DNA damage responses and hepatocyte proliferation, thereby promoting hepatocarcinogenesis in mice. Targeting this pathway may be an attractive approach for chemoprevention of hepatocellular carcinoma.</p></div>