Dual Oxidase2 and pancreatic adenocarcinoma: IFN-gamma-mediated dual oxidase2 overexpression results in H2O2-induced, ERKassociated up-regulation of HIF-1 alpha and VEGF-A

作者：Wu Yongzhong; Meitzler Jennifer L; Antony Smitha; Juhasz Agnes; Lu Jiamo; Jiang Guojian; Liu Han; Hollingshead Melinda; Haines Diana C; Butcher Donna; Panter Michaela S; Roy Krishnendu; Doroshow James H^*

来源：Oncotarget, 2016, 7(42): 68412-68433.

DOI：10.18632/oncotarget.12032

• dual oxidase
• NADPH oxidase
• pancreatic cancer
• hydrogen peroxide
• angiogenesis

Several NADPH oxidase family members, including dual oxidase 2 [DUOX2], are expressed in human tumors, particularly gastrointestinal cancers associated with long-standing chronic inflammation. We found previously that exposure of pancreatic ductal adenocarcinoma cells to the pro-inflammatory cytokine IFN-gamma increased DUOX2 expression (but not other NADPH oxidases) leading to long-lived H2O2 production. To elucidate the pathophysiology of DUOX2-mediated H2O2 formation in the pancreas further, we demonstrate here that IFN-gamma-treated BxPC-3 and CFPAC-1 pancreatic cancer cells (known to increase DUOX2 expression) produce significant levels of intracellular oxidants and extracellular H2O2 which correlate with concomitant upregulation of VEGF-A and HIF-1 alpha transcription. These changes are not observed in the PANC-1 line that does not increase DUOX2 expression following IFN-gamma treatment. DUOX2 knockdown with short interfering RNA significantly decreased IFN-gamma-induced VEGF-A or HIF-1 alpha up-regulation, as did treatment of pancreatic cancer cells with the NADPH oxidase inhibitor diphenylene iodonium, the multifunctional reduced thiol N-acetylcysteine, and the polyethylene glycol-modified form of the hydrogen peroxide detoxifying enzyme catalase. Increased DUOX2-related VEGF-A expression appears to result from reactive oxygen-mediated activation of ERK signaling that is responsible for AP-1-related transcriptional effects on the VEGF-A promoter. To clarify the relevance of these observations in vivo, we demonstrate that many human premalignant pancreatic intraepithelial neoplasms and frank pancreatic cancers express substantial levels of DUOX protein compared to histologically normal pancreatic tissues, and that expression of both DUOX2 and VEGF-A mRNAs is significantly increased in surgically-resected pancreatic cancers compared to the adjacent normal pancreas.

• 出版日期2016-10-18