Navigating the ERK1/2 MAPK Cascade

被引:32
|
作者
Martin-Vega, Ana [1 ]
Cobb, Melanie H. [1 ,2 ]
机构
[1] UT Southwestern Med Ctr, Dept Pharmacol, 6001 Forest Pk Rd, Dallas, TX 75390 USA
[2] UT Southwestern Med Ctr, Simmons Comprehens Canc Ctr, 6001 Forest Pk Rd, Dallas, TX 75390 USA
关键词
ERK1/2; MAPKs; cancer; scaffold; therapies; inhibitors; ACTIVATED PROTEIN-KINASE; SIGNAL-REGULATED KINASE; EPIDERMAL-GROWTH-FACTOR; SELECTIVE MEK1/2 INHIBITOR; IQGAP1 INTEGRATES CA2+/CALMODULIN; NEGATIVE FEEDBACK-REGULATION; EFFECTOR DOMAIN PROTEIN; RASGAP-RELATED PROTEIN; EMBRYONIC STEM-CELLS; OF-FUNCTION MUTATION;
D O I
10.3390/biom13101555
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
The RAS-ERK pathway is a fundamental signaling cascade crucial for many biological processes including proliferation, cell cycle control, growth, and survival; common across all cell types. Notably, ERK1/2 are implicated in specific processes in a context-dependent manner as in stem cells and pancreatic beta-cells. Alterations in the different components of this cascade result in dysregulation of the effector kinases ERK1/2 which communicate with hundreds of substrates. Aberrant activation of the pathway contributes to a range of disorders, including cancer. This review provides an overview of the structure, activation, regulation, and mutational frequency of the different tiers of the cascade; with a particular focus on ERK1/2. We highlight the importance of scaffold proteins that contribute to kinase localization and coordinate interaction dynamics of the kinases with substrates, activators, and inhibitors. Additionally, we explore innovative therapeutic approaches emphasizing promising avenues in this field.
引用
收藏
页数:48
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