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Extracellular signal-regulated kinase 1 (ERK1, MAPK3) and Extracellular signal-regulated kinase 2 (ERK2, MAPK1) (ERK1 (MAPK3), ERK2 (MAPK1))

Target
ERK1 (MAPK3), ERK2 (MAPK1)
Molecular classification
Enzyme (protein-serine/threonine kinase), Signal transduction protein, Member of the MAP kinase family (Mitogen-activated protein kinases)
01

Overview

Extracellular signal-regulated kinase 1 and 2 are highly conserved serine/threonine kinases, encoded by the MAPK3 and MAPK1 genes, respectively. They act as the final effectors in the canonical MAPK/ERK signaling cascade. Activated by upstream MEK1/2 kinases (which are in turn activated by Raf kinases in response to extracellular signals such as growth factors), ERK1/2 phosphorylate numerous cytoplasmic and nuclear substrates, including transcription factors (e.g., ELK1, c-Fos, JunB), cytoskeletal proteins, and additional regulatory molecules. ERK1/2 control critical cell functions such as cell cycle progression, survival, differentiation, migration, and transcription. Dysregulation of ERK1/2 activity is implicated in oncogenesis, making them key cancer therapeutic targets. Drugs targeting the MAPK/ERK pathway, directly or indirectly, are in clinical use and development, but their broad roles in normal cellular physiology pose notable toxicity and resistance challenges.

Other names
ERK1ERK2MAPK3 (for ERK1)MAPK1 (for ERK2)Extracellular signal-regulated kinase 1Extracellular signal-regulated kinase 2Mitogen-activated protein kinase 1/2p44 MAPK (ERK1)p42 MAPK (ERK2)
02

Mechanism of action

Inhibition of ERK1/2 phosphorylation (inhibiting kinase activity); Disruption of downstream transcription factor activation; Cell cycle arrest through cyclin-dependent kinase inhibitors

03

Biological functions

Signal transductionCell proliferationCell cycle progressionCell survivalCell differentiationApoptosisCell migrationMetabolismRegulation of transcription
04

Disease associations

Cancer (increased ERK activity is found in ~1/3 of human cancers)InflammationNeurodegenerative diseaseCardiovascular disease
05

Safety considerations

Toxicity due to broad pathway involvement in normal cell functions (rash, diarrhea, fatigue, cardiac effects with pathway inhibitors)Rapid development of resistance in cancer therapy due to pathway redundancyOff-target effects from interfering with physiological MAPK signaling
06

Interacting drugs

Trametinib, cobimetinib, binimetinib (MEK1/2 inhibitors indirectly affect ERK1/2)

2 more in the full profile.

07

Biomarkers

Phosphorylated ERK1/2 (p-ERK) levels in tumors/tissues for patient selection and efficacy monitoring

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