内质网
未折叠蛋白反应
细胞凋亡
体内
卡尔帕因
癌症
细胞生物学
癌症研究
半胱氨酸蛋白酶
癌细胞
半胱氨酸蛋白酶12
化学
医学
程序性细胞死亡
生物
生物化学
内科学
酶
生物技术
作者
Jialin Li,Kan Chen,Jianhua Huang,Dongqing Chu,Miaomiao Tian,Keqiang Huang,Chunyu Ma
标识
DOI:10.3389/fphar.2021.690612
摘要
From a mechanistic perspective, AA treatment was associated with increases in levels of calcium and the calcium- dependent protease calpain, and it further induced endoplasmic reticulum (ER) stress and consequent Grp78-related IRE1α and JNK phosphorylation, ultimately driving caspase-3 activation and apoptotic death. Together, these results highlight AA as a promising tool for the therapeutic treatment of tongue cancer in clinical practice.
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