Elevated NR2F1 Underlies the Persistence of Invasive Disease After Treatment of Braf-Mutant Melanoma

Authors

Manoela Tiago
Timothy J Purwin
Casey D Stefanski
Renaira Oliveira da Silva
Mitchell E Fane
Yash Chhabra
Jelan I Haj
Jessica Lf Teh
Rama Kadamb
Weijia Cai
Sheera R Rosenbaum
Vivian Chua
Nir Hacohen
Michael A Davies
Jessie Villanueva
Inna Chervoneva
Ashani T Weeraratna
Dan A Erkes
Claudia Capparelli
Julio A Aguirre-Ghiso
Andrew E Aplin

Language

English

Publication Date

9-16-2025

Journal

The Journal of Clinical Investigation

DOI

10.1172/JCI178446

PMID

40955663

PMCID

PMC12435839

PubMedCentral® Posted Date

7-29-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Despite the success of targeted inhibitors in cutaneous melanoma, therapeutic responses are limited by the aged tumor microenvironment and drug-tolerant residual cells. Given the similarities between drug tolerance and cellular dormancy, we studied the dormancy marker, nuclear receptor subfamily 2 group F member 1 (NR2F1), in response to BRAF-V600E inhibitors (BRAFi) plus MEK inhibitors (MEKi) in BRAF-mutant melanoma models. Transcriptomic analysis of melanoma patient samples treated with BRAFi + MEKi showed increased NR2F1. NR2F1 was highly expressed in the drug-tolerant invasive cell state of minimal residual disease in patient-derived and mouse-derived xenografts on BRAFi + MEKi. NR2F1 over-expression was sufficient to reduce BRAFi + MEKi effects on tumor growth in vivo, and cell proliferation, death, and invasion in vitro. Effects were linked to genes involved in mTORC1 signaling. These cells were sensitive to the combination of BRAFi, MEKi plus rapamycin. Melanomas from aged mice, known to exhibit decreased responses to BRAFi + MEKi, displayed higher levels of NR2F1 compared to tumors from young mice. Depleting NR2F1 in an aged mouse melanomas improved the response to targeted therapy. These findings show high NR2F1 expression in 'invasive-state' residual cells and that targeting NR2F1-high cells with mTORC1 inhibitors may improve outcomes in patients with melanoma.

Keywords

Melanoma, Animals, Humans, Proto-Oncogene Proteins B-raf, Mice, COUP Transcription Factor I, Neoplasm Invasiveness, Mutation, Cell Line, Tumor, Protein Kinase Inhibitors, Skin Neoplasms, Neoplasm Proteins, Xenograft Model Antitumor Assays, Female, Oncology, Therapeutics, Drug therapy, Melanoma

Published Open-Access

yes

Recommended Citation

Tiago, Manoela; Purwin, Timothy J; Stefanski, Casey D; et al., "Elevated NR2F1 Underlies the Persistence of Invasive Disease After Treatment of Braf-Mutant Melanoma" (2025). Faculty, Staff and Student Publications. 5511.
https://digitalcommons.library.tmc.edu/uthgsbs_docs/5511