Abstract 5988: MEK1/2 degraders uncover kinase-independent role of MEK1/2 in CRAF stabilization and maturation

Abstract The mitogen-activated protein kinase (MAPK) cascade is an evolutionarily conserved signaling pathway comprised of RAS GTPases, and downstream effector kinases (RAF, MEK, and ERK) that promote cell growth and survival. MEK1 and MEK2 (MEK1/2) are ubiquitous members of the dual-specificity MAP2K kinase family that phosphorylate and activate ERK1/2, controlling cellular proliferation. MEK1/2 paralogs share highly similar kinase domains, including their activation loops, which are phosphorylated by the upstream RAF family of kinases ARAF, BRAF, and CRAF. The activation of MEK1/2 by RAF is thoroughly described; RAF directly interacts with and phosphorylates MEK1/2, resulting in MEK1/2 kinase activation and subsequent phosphorylation of ERK1/2. In contrast, how the upstream RAF kinase, particularly CRAF, is activated is highly complex, involving an orchestration of chaperones, phosphorylation, and RAF dimerization, ultimately resulting in the phosphorylation of MEK1/2. The recognized CRAF signaling cascade has MEK1/2 functioning solely as a substrate of CRAF, binding to CRAF after RAS binding and RAF dimerization. However, there is evidence that MEK1 can directly regulate CRAF activity independent of RAS, suggesting that MEK1 has additional functions in the CRAF cycle. Here, using MEK1/2 proteolysis targeting chimeras (PROTACs), we discovered that MEK1/2 have kinase-independent functions in the regulation of CRAF protein stabilization, maturation, and kinase activation. Our findings reshape the current view of the CRAF activation cycle, establishing MEK1/2 binding to CRAF as an early required stabilizing event preceding CRAF-RAS engagement. Thus, MEK1/2 functions as both an activator and substrate of CRAF. Citation Format: Jason S. Wasserman, Alison M. Kurimchak, Carlos Herrera-Montávez, Glenn A. Doyle, Brandon D. Fox, Ishadi K. Kodikara, Jian Jin, James S. Duncan. MEK1/2 degraders uncover kinase-independent role of MEK1/2 in CRAF stabilization and maturation [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5988.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-5988
Primary Topic
Melanoma and MAPK Pathways
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article
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article

Abstract 5988: MEK1/2 degraders uncover kinase-independent role of MEK1/2 in CRAF stabilization and maturation

Carlos Herrera-Montávez, Glenn A. Doyle, James S. Duncan, Alison Kurimchak et al.
Cancer Research
Melanoma and MAPK Pathways
article

Abstract 5988: MEK1/2 degraders uncover kinase-independent role of MEK1/2 in CRAF stabilization and maturation

Carlos Herrera-Montávez, Glenn A. Doyle, James S. Duncan, Alison Kurimchak, Jason S. Wasserman, Ishadi K. M. Kodikara, Brandon D. Fox, Jian Jin
article en

Abstract

Abstract The mitogen-activated protein kinase (MAPK) cascade is an evolutionarily conserved signaling pathway comprised of RAS GTPases, and downstream effector kinases (RAF, MEK, and ERK) that promote cell growth and survival. MEK1 and MEK2 (MEK1/2) are ubiquitous members of the dual-specificity MAP2K kinase family that phosphorylate and activate ERK1/2, controlling cellular proliferation. MEK1/2 paralogs share highly similar kinase domains, including their activation loops, which are phosphorylated by the upstream RAF family of kinases ARAF, BRAF, and CRAF. The activation of MEK1/2 by RAF is thoroughly described; RAF directly interacts with and phosphorylates MEK1/2, resulting in MEK1/2 kinase activation and subsequent phosphorylation of ERK1/2. In contrast, how the upstream RAF kinase, particularly CRAF, is activated is highly complex, involving an orchestration of chaperones, phosphorylation, and RAF dimerization, ultimately resulting in the phosphorylation of MEK1/2. The recognized CRAF signaling cascade has MEK1/2 functioning solely as a substrate of CRAF, binding to CRAF after RAS binding and RAF dimerization. However, there is evidence that MEK1 can directly regulate CRAF activity independent of RAS, suggesting that MEK1 has additional functions in the CRAF cycle. Here, using MEK1/2 proteolysis targeting chimeras (PROTACs), we discovered that MEK1/2 have kinase-independent functions in the regulation of CRAF protein stabilization, maturation, and kinase activation. Our findings reshape the current view of the CRAF activation cycle, establishing MEK1/2 binding to CRAF as an early required stabilizing event preceding CRAF-RAS engagement. Thus, MEK1/2 functions as both an activator and substrate of CRAF. Citation Format: Jason S. Wasserman, Alison M. Kurimchak, Carlos Herrera-Montávez, Glenn A. Doyle, Brandon D. Fox, Ishadi K. Kodikara, Jian Jin, James S. Duncan. MEK1/2 degraders uncover kinase-independent role of MEK1/2 in CRAF stabilization and maturation [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5988.

Cancer ResearchVol. 86(7_Supplement)
Fox Chase Cancer Center (US), Icahn School of Medicine at Mount Sinai (US)
Openalex Percentile: Top 8%
Melanoma and MAPK Pathways
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