Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University. 283 Tongzipo Road, Changsha, 410013, Hunan, China.
Laboratory of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Guilin Medical University, 15 Lequn Road, Guilin, 541001, Guangxi, China.
Cancer Lett. 2019 Sep 10;459:30-40. doi: 10.1016/j.canlet.2019.05.025. Epub 2019 May 23.
Phosphatidylinositol 3-kinase (PI3K)/AKT pathway regulates cell growth, proliferation, survival, mobility and invasion. Mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) pathway is also an important mitogenic signaling pathway involved in various cellular progresses. AKT, also named protein kinase B (PKB), is a primary mediator of the PI3K signaling pathway; and ERK at the end of MAPK signaling is the unique substrate and downstream effector of mitogen-activated protein/extracellular signal-regulated kinase (MEK). The AKT and ERK signaling are both aberrantly activated in a wide range of human cancers and have long been targeted for cancer therapy, but the clinical benefits of these targeted therapies have been limited due to complex cross-talk. Novel strategies, such as AKT/ERK dual inhibitors, may be needed.
磷脂酰肌醇 3-激酶(PI3K)/AKT 途径调节细胞生长、增殖、存活、迁移和侵袭。丝裂原激活的蛋白激酶(MAPK)/细胞外信号调节激酶(ERK)途径也是参与各种细胞进程的重要有丝分裂信号通路。AKT,也称为蛋白激酶 B(PKB),是 PI3K 信号通路的主要介质;而 MAPK 信号通路末端的 ERK 是丝裂原激活蛋白/细胞外信号调节激酶(MEK)的独特底物和下游效应物。AKT 和 ERK 信号在广泛的人类癌症中均异常激活,长期以来一直是癌症治疗的靶点,但由于复杂的交叉对话,这些靶向治疗的临床获益有限。可能需要新的策略,如 AKT/ERK 双重抑制剂。