E3 ligase LMO7 enhances temozolomide sensitivity by promoting MGMT degradation in lung cancer
Abstract
-methylguanine-DNA methyltransferase (MGMT). Here, we identify the E3 ubiquitin ligase LIM domain only 7 (LMO7) as a regulator of TMZ sensitivity in NSCLC cells by promoting MGMT degradation. LMO7 directly binds MGMT via its F-box domain and promotes K48-linked polyubiquitination and proteasomal degradation of MGMT, thereby increasing TMZ sensitivity. TMZ treatment further strengthens the LMO7-MGMT interaction, creating a positive feedback loop that accelerates MGMT degradation and enhances TMZ sensitivity. Consistently, TMZ further strengthened the LMO7-MGMT interaction, and this enhancement was attenuated with the catalytically inactive MGMT-C145A mutant. In patient datasets, lower LMO7 expression and higher MGMT expression correlate with shorter overall survival in lung cancer (Kaplan-Meier Plotter analysis, p < 0.01). Together, these results indicate that LMO7-mediated MGMT degradation increases TMZ sensitivity in NSCLC, positioning LMO7 as a potential prognostic biomarker and therapeutic target.
Fields of Study & Subjects
Protein Degradation and Inhibitors
Lung Cancer Treatments and Mutations
Cancer-related Molecular Pathways
Publication details
- Journal / source
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Volume
- 302
- Issue
- 4
- Pages
- 111331–111331
- Publication date
- 27 February 2026
- Language
- EN