糖酵解
癌症研究
结直肠癌
瓦博格效应
慢性应激
细胞生长
血管生成
生物
癌症
内科学
内分泌学
医学
生物化学
新陈代谢
作者
Yunfeng Guan,Yao Wang,Hao Yu,Ying Feng,Yiyang Zhao,Xiangyang Zhan,Yan Wang
摘要
Colorectal cancer (CRC) is a common malignancy worldwide, and chronic stress has been considered as a significant risk factor for CRC.However, the role of chronic stress in CRC progression is unclear.The present study showed that pre-exposure to chronic stress facilitated CRC tumor growth in mice, and epinephrine promoted CRC cell proliferation in vitro.Metabolomics analysis revealed that chronic stress reshaped metabolic pathways to enhance glycolysis.Additional studies have shown that stress enhanced the expression levels of glycolytic-associated enzymes, including GLUT1, HK2 and PFKP.Mechanistically, chronic stress activated the β2-AR/PKA/CREB1 pathway, as a result, phosphorylated CREB1 transcriptional induced glycolytic enzymes expression.Furthermore, stress-induced cell proliferation and tumor growth could be reversed by administration of glycolysis inhibitor 2-deoxyglucose (2-DG) and β2-AR antagonist ICI118,551, respectively.Altogether, these findings define novel insights into the stress-induced epinephrine-mediated CRC progression from the point of view of tumor energy metabolism reprogramming and provide a perspective on targeting glycolysis as a potential approach in stress-associated CRC treatment.
科研通智能强力驱动
Strongly Powered by AbleSci AI