Abstract 3623: Effects of the anti-obesity medication tirzepatide on the tumor microenvironment in a mouse model of obesity-associated, hormone-dependent breast cancer

Abstract Numerous anti-obesity agents have been approved for obesity/diabetes treatment, but their impact on obesity-related breast cancer is not clear. Our pilot data supported a trend for reduced growth of estrogen-receptor positive (ER+) tumors with tirzepatide (TZP), an FDA-approved incretin mimetic targeting both GLP-1 and GIP receptors. Here, our goal was to determine if TZP-induced changes in the mammary tumor microenvironment contributed to the anti-cancer effects of TZP. Female C57/BL6 mice were fed a 46% high-fat diet to induce obesity. They were then randomized to receive tirzepatide (15-week dose escalation to 75nM) or vehicle for the duration of the study. Three weeks after starting TZP, tumors were initiated by injection of estrogen-receptor positive Py230 cells, and tumor volumes were measured twice weekly. Mice were terminated when tumor volumes reached humane endpoints, or after 16 weeks of treatment. Mammary adipose tissue was collected at the end of the study and processed for histological examination. Adipocyte size was assessed in H&E stained tissues using the Adiposoft plugin for ImageJ, and number of macrophages in the tumor microenvironment was assessed using Mac2 immunofluorescence staining. As expected, TZP induced ∼20% weight loss, which was reflected in both an increase in the proportion of small adipocytes and a reduction in the number of large adipocytes in the tumor microenvironment (mammary gland). This suggests that changes in macrophage infiltration are not likely to contribute to the potential anti-cancer effects of TZP in our pilot studies. Ongoing studies will address additional mechanisms by which TZP affects tumors and/or the obese tumor microenvironment. Citation Format: Charlotte E. Gibson, Amanda L. Kucinskas, Emma G. Bailey, Flora Tao, Katherine E. Sanchez, Katherine L. Cook, Erin D. Giles. Effects of the anti-obesity medication tirzepatide on the tumor microenvironment in a mouse model of obesity-associated, hormone-dependent breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3623.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-3623
Primary Topic
Cancer Risks and Factors
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 3623: Effects of the anti-obesity medication tirzepatide on the tumor microenvironment in a mouse model of obesity-associated, hormone-dependent breast cancer

Katherine Sánchez, Charlotte Gibson, Erin D. Giles, Amanda L. Kucinskas et al.
Cancer Research
Cancer Risks and Factors
article

Abstract 3623: Effects of the anti-obesity medication tirzepatide on the tumor microenvironment in a mouse model of obesity-associated, hormone-dependent breast cancer

Katherine Sánchez, Charlotte Gibson, Erin D. Giles, Amanda L. Kucinskas, Flora Tao, K. L. Cook
article en

Abstract

Abstract Numerous anti-obesity agents have been approved for obesity/diabetes treatment, but their impact on obesity-related breast cancer is not clear. Our pilot data supported a trend for reduced growth of estrogen-receptor positive (ER+) tumors with tirzepatide (TZP), an FDA-approved incretin mimetic targeting both GLP-1 and GIP receptors. Here, our goal was to determine if TZP-induced changes in the mammary tumor microenvironment contributed to the anti-cancer effects of TZP. Female C57/BL6 mice were fed a 46% high-fat diet to induce obesity. They were then randomized to receive tirzepatide (15-week dose escalation to 75nM) or vehicle for the duration of the study. Three weeks after starting TZP, tumors were initiated by injection of estrogen-receptor positive Py230 cells, and tumor volumes were measured twice weekly. Mice were terminated when tumor volumes reached humane endpoints, or after 16 weeks of treatment. Mammary adipose tissue was collected at the end of the study and processed for histological examination. Adipocyte size was assessed in H&E stained tissues using the Adiposoft plugin for ImageJ, and number of macrophages in the tumor microenvironment was assessed using Mac2 immunofluorescence staining. As expected, TZP induced ∼20% weight loss, which was reflected in both an increase in the proportion of small adipocytes and a reduction in the number of large adipocytes in the tumor microenvironment (mammary gland). This suggests that changes in macrophage infiltration are not likely to contribute to the potential anti-cancer effects of TZP in our pilot studies. Ongoing studies will address additional mechanisms by which TZP affects tumors and/or the obese tumor microenvironment. Citation Format: Charlotte E. Gibson, Amanda L. Kucinskas, Emma G. Bailey, Flora Tao, Katherine E. Sanchez, Katherine L. Cook, Erin D. Giles. Effects of the anti-obesity medication tirzepatide on the tumor microenvironment in a mouse model of obesity-associated, hormone-dependent breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3623.

Cancer ResearchVol. 86(7_Supplement)
Johns Hopkins University (US), University of Michigan (US), Wake Forest University (US), University of Baltimore (US)
Good health and well-being
Openalex Percentile: Top 18%
Cancer Risks and Factors
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.