NADPH Oxidase Promotes Pancreatic Cancer Cell Survival via Inhibiting JAK2 Dephosphorylation by Tyrosine Phosphatases

阅读量:

57

摘要:

Background & Aims:Growth factors, such as insulin-like growth factor-1 (IGF-I), protect pancreatic cancer (PaCa) cells from death. We recently showed that reactive oxygen species (ROS) produced by nicotinamide adenine dinucleotide phosphate (NADPH) oxidase Nox4 mediate the antiapoptotic effect of growth factors. Here, we examine the mechanisms of the antiapoptotic role of NADPH oxidase. We hypothesized that ROSs produced by NADPH oxidase inhibit key protein tyrosine phosphatases (PTPs) and thus sustain the activation of kinases mediating antiapoptotic pathways in PaCa cells.Methods:Transfections and pharmacologic inhibition were used to assess the effects of NADPH oxidase on Janus kinase 2 (JAK2) kinase, the low molecular weight–protein tyrosine phosphatase (LMW-PTP), and apoptosis.Results:We found that 1 target of ROSs is JAK2, an important antiapoptotic kinase in PaCa cells. Both serum-induced and IGF-I biphasic JAK2 phosphorylation, with a rapid (minutes) and transient first phase, and a slow and sustained (24–72 hours) second phase. Nox4 mediated the sustained phase of JAK2 phosphorylation, which was required for the antiapoptotic effects of IGF-I and serum. Transfection experiments identified the LMW-PTP as a negative regulator of sustained JAK2 phosphorylation. Growth factors inhibited LMW-PTP through its oxidation by NADPH oxidase. LMW-PTP colocalizes with Nox4 both in PaCa cells and in human pancreatic adenocarcinoma.Conclusions:The results suggest a novel signaling pathway, in which NADPH oxidase activation results in inhibition of PTPs, such as LMW-PTP, leading, in turn, to enhanced and sustained phosphorylation of kinases, such as JAK2, and suppression of apoptosis. This pathway mediates the prosurvival effect of ROSs and suggests new targets for pancreatic cancer treatment.

展开

DOI:

10.1053/j.gastro.2007.08.022

被引量:

314

年份:

2007

通过文献互助平台发起求助,成功后即可免费获取论文全文。

我们已与文献出版商建立了直接购买合作。

你可以通过身份认证进行实名认证,认证成功后本次下载的费用将由您所在的图书馆支付

您可以直接购买此文献,1~5分钟即可下载全文,部分资源由于网络原因可能需要更长时间,请您耐心等待哦~

身份认证 全文购买

相似文献

参考文献

引证文献

辅助模式

0

引用

文献可以批量引用啦~
欢迎点我试用!

引用