Döppler Heike, Storz Peter
Department of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Mayo Clinic , Jacksonville, FL , USA.
Front Oncol. 2017 Mar 15;7:41. doi: 10.3389/fonc.2017.00041. eCollection 2017.
Due to alterations in their metabolic activity and decreased mitochondrial efficiency, cancer cells often show increased generation of reactive oxygen species (ROS), but at the same time, to avoid cytotoxic signaling and to facilitate tumorigenic signaling, have mechanism in place that keep ROS in check. This requires signaling molecules that convey increases in oxidative stress to signal to the nucleus to upregulate antioxidant genes. Protein kinase D1 (PKD1), the serine/threonine kinase, is one of these ROS sensors. In this mini-review, we highlight the mechanisms of how PKD1 is activated in response to oxidative stress, so far known downstream effectors, as well as the importance of PKD1-initiated signaling for development and progression of pancreatic cancer.
由于癌细胞代谢活性的改变和线粒体效率的降低,它们通常表现出活性氧(ROS)生成增加,但与此同时,为了避免细胞毒性信号传导并促进致瘤信号传导,癌细胞具备控制ROS水平的机制。这需要信号分子将氧化应激的增加传递给细胞核,以上调抗氧化基因。丝氨酸/苏氨酸激酶蛋白激酶D1(PKD1)就是这些ROS传感器之一。在本综述中,我们重点介绍了PKD1如何响应氧化应激而被激活的机制、目前已知的下游效应器,以及PKD1启动的信号传导对胰腺癌发生和发展的重要性。