Supplementary Fig. 1 from Targeting the ERα DBD–LBD Interface with Mitoxantrone Disrupts Receptor Function through Proteasomal Degradation
Abstract
Supplementary Fig. 1: MTO, unlike fulvestrant, maintains E2-mediated ER-SRC3 interaction
Fields of Study & Subjects
Melanoma and MAPK Pathways
Protein Degradation and Inhibitors
Protein Kinase Regulation and GTPase Signaling
Publication details
- Publisher
- American Association for Cancer Research (AACR)
- Publication date
- 2 January 2026