2. Academic Validation
  3. Imlunestrant a next-generation oral SERD overcomes ESR1 mutant resistance in estrogen receptor-positive breast cancer

Imlunestrant a next-generation oral SERD overcomes ESR1 mutant resistance in estrogen receptor-positive breast cancer

  • JCI Insight. 2025 May 6;10(12):e188051. doi: 10.1172/jci.insight.188051.
Shira Sherman 1,  Zachary M Sandusky 1 2,  Douglas Russo 1 3 4,  David Zak 5,  Agostina Nardone 1,  Delia Friel 1 2,  Francisco Hermida-Prado 1,  Capucine Heraud 1,  Genevra Kuziel 1,  Ana Verma 3 6 7,  Giorgio Gaglia 3 6 7,  Sheheryar Kabraji 1 3 8,  Quang-De Nguyen 9,  Sandro Santagata 3 6 7,  Sean W Fanning 5,  Rinath Jeselsohn 1 2 3 8
Affiliations

Affiliations

  • 1 Department of Medical Oncology and.
  • 2 Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • 3 Harvard Medical School, Boston, Massachusetts, USA.
  • 4 Department of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
  • 5 Department of Cancer Biology, Loyola University Stritch School of Medicine, Maywood, Illinois, USA.
  • 6 Ludwig Center at Harvard and.
  • 7 Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • 8 Susan F. Smith Center for Women's Cancers and.
  • 9 Lurie Family Imaging Center, Center for Biomedical Imaging in Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
PMID: 40327396 DOI: 10.1172/jci.insight.188051
Abstract

Estrogen receptor α (ER) is a critical driver of tumorigenesis and tumor progression in most breast cancers. Endocrine therapies (ET) targeting ER are central to treating hormone receptor-positive breast Cancer, but resistance poses a clinical challenge. Some resistance mechanisms, particularly those involving estrogen-independent activity such as the ESR1 mutations, rely on ER signaling, supporting the need for next-generation ET. We investigated the preclinical efficacy of imlunestrant, an oral selective ER degrader, in ER-positive breast Cancer preclinical models, including models harboring the Y537S ESR1 mutation, an activating mutation. Imlunestrant demonstrated antagonistic activity and effective degradation of both WT and mutant ER, resulting in cell growth suppression. In vivo, imlunestrant outperformed fulvestrant, leading to tumor regression in a patient-derived xenograft harboring the Y537S ESR1 mutation. Cyclic mutiplexed immunofluorescence and transcriptomic analysis revealed enhanced cell cycle arrest and downregulation of estrogen-responsive genes with imlunestrant treatment. Additionally, a genome-wide CRISPR knock-out screen identified several vulnerabilities that were either persistent or acquired after imlunestrant treatment, providing a rationale for future studies of combination treatments with imlunestrant. Collectively, these results highlight the on-target and selective activity of imlunestrant, which can circumvent resistance engendered by the Y537S ESR1 mutation.

Keywords

Breast cancer; Cell biology; Oncology.

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