ROS mediated EGFR/MEK/ERK/HIF-1α Loop Regulates Glucose metabolism in pancreatic cancer

被引:50
|
作者
Wang, Gang [1 ,2 ]
Li, Yifeng [3 ]
Yang, Zeyu [4 ]
Xu, Weina [5 ]
Yang, Yifan [2 ]
Tan, Xiaodong [2 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Emergency Med, Shenyang 110004, Liaoning, Peoples R China
[2] China Med Univ, Shengjing Hosp, Dept Gen Surg, 36 Sanhao St, Shenyang 110004, Liaoning, Peoples R China
[3] China Med Univ, Clin Dept 1, 101K, Shenyang 110122, Liaoning, Peoples R China
[4] China Med Univ, Shengjing Hosp, Dept Ultrasound, Shenyang 110004, Liaoning, Peoples R China
[5] China Med Univ, Shengjing Hosp, Dept Radiol & Nucl Med, Shenyang 110004, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Pancreatic cancer; Glycometabolism; HIF-1; alpha; EGFR/MEK/ ERK pathway; ROS; CELL-DISSOCIATION; INVASION-METASTASIS; HYPOXIA; EXPRESSION; INVOLVEMENT; PROMOTES; HIF-1; ACTIVATION; INDUCTION; RESPONSES;
D O I
10.1016/j.bbrc.2018.04.177
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To investigate the glycometabolism associated mechanism in invasion and metastasis of pancreatic cancer. We screened out genes involved in anaerobic glycolysis headed by HIF-1 alpha,using pre-established a pair of pancreatic cancer cell lines. In this study, we further detected the glucose metabolism state not only in the cells but all also in two groups of patients with different SUVmax on F-18-FDG PET/CT. The data suggests that ROS mediated EGFR/MEK/ERK/HIF-1 alpha loop is activated in high glucose metabolic samples both in vitro and in vivo: The increasing of HIF-1 alpha expression is controlled by activation of EGFR/MEK/ERK pathway in hypoxia condition, HlF-l alpha inhibits excessive release of ROS, the reduction of ROS further activates EGFR to form a positive feedback loop. This difference is closely related to invasion and metastasis capacity of pancreatic cancer, and can be rescued by separate or combined inhibition of EGFR or HIF-l alpha in various degree. These results indicate a new clue to develop therapy of pancreatic cancer by regulating the glucose metabolism. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:873 / 878
页数:6
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