Modulating the tumor microenvironment improves antitumor effect of anti-PD-L1 mAb in breast cancer

Introduction: Immune checkpoint inhibitors (ICIs) have provided noteworthy benefits in multiple cancer patients. However, the efficacy of monotherapy of ICIs was very limited. In this study, we endeavored to explore whether losartan can modulate the solid tumor microenvironment (TME) and improve the...

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Main Authors: Xiuying Li, Xianqin Luo, Shunqin Hu
Format: Article
Language:English
Published: Tabriz University of Medical Sciences 2023-03-01
Series:BioImpacts
Subjects:
Online Access:https://bi.tbzmed.ac.ir/PDF/bi-13-89.pdf
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author Xiuying Li
Xianqin Luo
Shunqin Hu
author_facet Xiuying Li
Xianqin Luo
Shunqin Hu
author_sort Xiuying Li
collection DOAJ
description Introduction: Immune checkpoint inhibitors (ICIs) have provided noteworthy benefits in multiple cancer patients. However, the efficacy of monotherapy of ICIs was very limited. In this study, we endeavored to explore whether losartan can modulate the solid tumor microenvironment (TME) and improve the therapeutic efficacy of anti-PD-L1 mAb in 4T1 mouse breast tumor model and the underlying mechanism. Methods: The tumor-bearing mice were treated with control agents, losartan, anti-PD-L1 mAb or the dual agents. The blood and tumor tissues were respectively used for ELISA and immunohistochemical analysis. CD8-depletion and lung metastatic experiments were performed. Results: Compared to control group, losartan inhibited the expression of alpha-smooth muscle actin (α-SMA), deposition of collagen I in the tumor tissues. The concentration of transforming growth factor-β1 (TGF-β1) in the serum was low in the losartan treated group. Although losartan alone was ineffective, the combination of losartan and anti-PD-L1 mAb elicited dramatic antitumor effect. Immunohistochemical analysis revealed that there were more intra-tumoral infiltration of CD8+ T cells and increased granzyme B production in the combination therapy group. In addition, the size of spleen was smaller in the combination therapy group, compared to monotherapy. The CD8-depleting Abs abrogated the antitumor efficacy of losartan and anti-PD-L1 mAb in vivo. The combination of losartan and anti-PD-L1 mAb significantly inhibited 4T1 tumor cells lung metastatic in vivo. Conclusion: Our results indicated that losartan can modulate the tumor microenvironment, and improve the efficacy of anti-PD-L1 mAb.
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spelling doaj.art-eddc149e8acb4b1783be25cc03d12e692023-04-16T06:58:18ZengTabriz University of Medical SciencesBioImpacts2228-56602228-56522023-03-01132899610.34172/bi.2023.24166bi-24166Modulating the tumor microenvironment improves antitumor effect of anti-PD-L1 mAb in breast cancerXiuying Li0Xianqin Luo1Shunqin Hu2Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, ChinaCollege of Traditional Chinese Medicine, Chongqing Medical University; Chongqing, ChinaDepartment of Gynecology and Obstetrics, the First Affiliated Hospital of Kunming Medical University, Kunming, ChinaIntroduction: Immune checkpoint inhibitors (ICIs) have provided noteworthy benefits in multiple cancer patients. However, the efficacy of monotherapy of ICIs was very limited. In this study, we endeavored to explore whether losartan can modulate the solid tumor microenvironment (TME) and improve the therapeutic efficacy of anti-PD-L1 mAb in 4T1 mouse breast tumor model and the underlying mechanism. Methods: The tumor-bearing mice were treated with control agents, losartan, anti-PD-L1 mAb or the dual agents. The blood and tumor tissues were respectively used for ELISA and immunohistochemical analysis. CD8-depletion and lung metastatic experiments were performed. Results: Compared to control group, losartan inhibited the expression of alpha-smooth muscle actin (α-SMA), deposition of collagen I in the tumor tissues. The concentration of transforming growth factor-β1 (TGF-β1) in the serum was low in the losartan treated group. Although losartan alone was ineffective, the combination of losartan and anti-PD-L1 mAb elicited dramatic antitumor effect. Immunohistochemical analysis revealed that there were more intra-tumoral infiltration of CD8+ T cells and increased granzyme B production in the combination therapy group. In addition, the size of spleen was smaller in the combination therapy group, compared to monotherapy. The CD8-depleting Abs abrogated the antitumor efficacy of losartan and anti-PD-L1 mAb in vivo. The combination of losartan and anti-PD-L1 mAb significantly inhibited 4T1 tumor cells lung metastatic in vivo. Conclusion: Our results indicated that losartan can modulate the tumor microenvironment, and improve the efficacy of anti-PD-L1 mAb.https://bi.tbzmed.ac.ir/PDF/bi-13-89.pdfanti-pd-l1 mablosartantumor microenvironmentimmunotherapy
spellingShingle Xiuying Li
Xianqin Luo
Shunqin Hu
Modulating the tumor microenvironment improves antitumor effect of anti-PD-L1 mAb in breast cancer
BioImpacts
anti-pd-l1 mab
losartan
tumor microenvironment
immunotherapy
title Modulating the tumor microenvironment improves antitumor effect of anti-PD-L1 mAb in breast cancer
title_full Modulating the tumor microenvironment improves antitumor effect of anti-PD-L1 mAb in breast cancer
title_fullStr Modulating the tumor microenvironment improves antitumor effect of anti-PD-L1 mAb in breast cancer
title_full_unstemmed Modulating the tumor microenvironment improves antitumor effect of anti-PD-L1 mAb in breast cancer
title_short Modulating the tumor microenvironment improves antitumor effect of anti-PD-L1 mAb in breast cancer
title_sort modulating the tumor microenvironment improves antitumor effect of anti pd l1 mab in breast cancer
topic anti-pd-l1 mab
losartan
tumor microenvironment
immunotherapy
url https://bi.tbzmed.ac.ir/PDF/bi-13-89.pdf
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AT shunqinhu modulatingthetumormicroenvironmentimprovesantitumoreffectofantipdl1mabinbreastcancer