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Article

Single-Cell Transcriptomics Reveals Immune Modulation by Telmisartan in Colorectal Cancer

1
Institute of Medical Innovation and Research, Peking University Third Hospital, Beijing 100191, China
2
Medical Research Center, Peking University Third Hospital, Beijing 100191, China
3
Emergency Department, Peking University Third Hospital, Beijing 100191, China
4
Department of Medicine, School of Medicine, Stanford University, Stanford, CA 94305, USA
5
Division of Vascular Surgery, Department of Surgery, School of Medicine, Stanford University, Stanford, 94305 CA, USA
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Cells 2026, 15(8), 729; https://doi.org/10.3390/cells15080729
Submission received: 18 March 2026 / Revised: 14 April 2026 / Accepted: 17 April 2026 / Published: 20 April 2026

Abstract

Telmisartan, an angiotensin II type 1 receptor blocker with established anti-inflammatory and antihypertensive properties, has been reported to inhibit tumor cell proliferation, yet its impact on the tumor immune microenvironment remains poorly understood. In this study, we evaluated the immunomodulatory effects of telmisartan using a syngeneic MC38 colorectal cancer model in C57BL/6 mice. Daily intragastric administration of telmisartan significantly suppressed tumor growth and reduced endpoint tumor weight compared with controls. To elucidate the underlying mechanisms, we performed single-cell RNA sequencing on tumor-infiltrating CD45+ immune cells and revealed a macrophage-dominated immune landscape comprising multiple transcriptionally distinct subclusters. Telmisartan broadly downregulated pro-tumoral and M2-associated macrophage programs, including decreased expression of genes such as Mrc1 and Spp1, while also suppressing cell proliferation-related pathways. In contrast to its overall suppressive impact on macrophages, telmisartan increased the proportion of cytotoxic CD8+ T cells, reduced regulatory T cell counts, and enhanced major histocompatibility complex class I antigen presentation, consistent with an immune-activating effect. These results indicate that telmisartan reshapes the colorectal tumor immune microenvironment by simultaneously attenuating tumor-promoting macrophage activity and augmenting cytotoxic T cell responses. Overall, this study provides a single-cell framework to understand how angiotensin receptor blockade reshapes tumor-infiltrating immune programs, highlighting the translational potential of repurposing telmisartan for novel cancer immunotherapy strategies.
Keywords: telmisartan; colorectal cancer; tumor microenvironment; macrophage; T cell telmisartan; colorectal cancer; tumor microenvironment; macrophage; T cell

Share and Cite

MDPI and ACS Style

Li, J.; Yang, D.; Wang, X.; Ju, R.; Chen, S.; Zhao, J.; Xu, J.; Chen, J.; Ye, J.; Xu, B.; et al. Single-Cell Transcriptomics Reveals Immune Modulation by Telmisartan in Colorectal Cancer. Cells 2026, 15, 729. https://doi.org/10.3390/cells15080729

AMA Style

Li J, Yang D, Wang X, Ju R, Chen S, Zhao J, Xu J, Chen J, Ye J, Xu B, et al. Single-Cell Transcriptomics Reveals Immune Modulation by Telmisartan in Colorectal Cancer. Cells. 2026; 15(8):729. https://doi.org/10.3390/cells15080729

Chicago/Turabian Style

Li, Jinxin, Decao Yang, Xiaoyue Wang, Runqing Ju, Shaomeng Chen, Jingyi Zhao, Jiaxing Xu, Jiaxin Chen, Jiayu Ye, Baohui Xu, and et al. 2026. "Single-Cell Transcriptomics Reveals Immune Modulation by Telmisartan in Colorectal Cancer" Cells 15, no. 8: 729. https://doi.org/10.3390/cells15080729

APA Style

Li, J., Yang, D., Wang, X., Ju, R., Chen, S., Zhao, J., Xu, J., Chen, J., Ye, J., Xu, B., Yin, Q., & Wang, Y. (2026). Single-Cell Transcriptomics Reveals Immune Modulation by Telmisartan in Colorectal Cancer. Cells, 15(8), 729. https://doi.org/10.3390/cells15080729

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