Estrogens determine the efficacy of cancer immunotherapy in obese males with melanoma.

Although obesity is a major risk factor for cancer, it may also improve the response to cancer therapy. Here we investigated the impact of obesity on the efficacy of immune checkpoint inhibitors (ICI). In male mice, obesity promoted tumor growth but enhanced the response to ICI. This was associated with higher expression of immune-related genes within the tumor and enhanced infiltration of tumor-specific CD8+ T cells. Further, obesity in mice was associated with higher estrogen levels and enrichment of estrogen response genes in the tumor, and anti-PD-1 efficacy was reduced upon administration of the aromatase inhibitor letrozole, which blocks the production of estrogens. Mechanistically, adipocyte-derived estrogens increased antigen presentation by dendritic cells and tumor-specific CD8+ T-cell cytotoxicity. Lastly, overweight and obese male melanoma patients responded better to ICI, high estrogen levels being associated with improved response and survival. Our results suggest that estrogens may serve as a predictive factor of response to ICI in men with melanoma.

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Publication Details

Journal
Open Access CRIS of the University of Bern
Published
2025-06-12
DOI
https://doi.org/10.48620/89535
Primary Topic
Cancer Risks and Factors
Type
article
Field-Weighted Citation Impact
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article

Estrogens determine the efficacy of cancer immunotherapy in obese males with melanoma.

Open Access CRIS of the University of Bern
Cancer Risks and Factors
article

Estrogens determine the efficacy of cancer immunotherapy in obese males with melanoma.

article en

Abstract

Although obesity is a major risk factor for cancer, it may also improve the response to cancer therapy. Here we investigated the impact of obesity on the efficacy of immune checkpoint inhibitors (ICI). In male mice, obesity promoted tumor growth but enhanced the response to ICI. This was associated with higher expression of immune-related genes within the tumor and enhanced infiltration of tumor-specific CD8+ T cells. Further, obesity in mice was associated with higher estrogen levels and enrichment of estrogen response genes in the tumor, and anti-PD-1 efficacy was reduced upon administration of the aromatase inhibitor letrozole, which blocks the production of estrogens. Mechanistically, adipocyte-derived estrogens increased antigen presentation by dendritic cells and tumor-specific CD8+ T-cell cytotoxicity. Lastly, overweight and obese male melanoma patients responded better to ICI, high estrogen levels being associated with improved response and survival. Our results suggest that estrogens may serve as a predictive factor of response to ICI in men with melanoma.

Open Access CRIS of the University of Bern
Hypertension Institute (US), Institute of Pharmacology (CZ)
Good health and well-being
Openalex Percentile: Top 42%
Cancer Risks and Factors
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Estrogens determine the efficacy of cancer immunotherapy in obese males with melanoma. · Open Access CRIS of the University of Bern (2025) | TGRS Research Map | TGRS