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Updated: Jan 25, 2026

Visualization, Quantification, and Mapping of Immune Cell Populations in the Tumor Microenvironment
Published on: March 25, 2020
Anlotinib inhibits esophageal cancer malignancy by ameliorating the immune microenvironment
Zhao Minghong1, Yuan Lin1, Huang Xi1
1Department of Oncology, Jianhu People's Hospital, Yancheng, 224700, Jiangsu, China.
Abstract:
Esophageal cancer (EC) is a global health challenge with limited treatment and low efficacy. The role of vascular endothelial growth factor receptor 2 (VEGFR2) in EC has attracted significant attention. In this study, we found that anlotinib, an oral VEGFR2 inhibitor, exhibited a strong inhibitory effect on EC in vitro and in vivo. Moreover, VEGFR2 expression was positively correlated with infiltration levels of macrophages and dendritic cells (DCs) via comprehensive analysis and molecular experiment. Together, we evaluated the correlations between VEGFR2 expression and immune infiltration and explored the role of anlotinib on EC, providing a potential strategy for the intervention of EC.
Insights
Anlotinib, a VEGFR2 inhibitor, effectively suppresses esophageal cancer (EC) growth. This study links VEGFR2 expression to immune cell infiltration, suggesting anlotinib as a potential EC treatment strategy.
Area of Science:
- Oncology
- Cancer Research
- Immunology
Background:
- Esophageal cancer (EC) presents a significant global health burden with limited therapeutic options.
- Vascular endothelial growth factor receptor 2 (VEGFR2) has emerged as a key target in EC research.
Purpose of the Study:
- To investigate the inhibitory effect of anlotinib, an oral VEGFR2 inhibitor, on esophageal cancer.
- To evaluate the correlation between VEGFR2 expression and immune cell infiltration in EC.
- To explore the therapeutic potential of anlotinib in EC intervention.
Main Methods:
- In vitro and in vivo experiments were conducted to assess anlotinib's efficacy.
- Comprehensive analysis and molecular experiments were employed to study VEGFR2 expression.
- Immune cell infiltration levels, including macrophages and dendritic cells (DCs), were analyzed in relation to VEGFR2.
Main Results:
- Anlotinib demonstrated significant inhibitory effects on esophageal cancer progression both in vitro and in vivo.
- VEGFR2 expression was found to be positively correlated with the infiltration levels of macrophages and dendritic cells (DCs).
Conclusions:
- Anlotinib exhibits potent anti-cancer activity against esophageal cancer.
- VEGFR2 plays a role in modulating the tumor immune microenvironment in EC.
- Targeting VEGFR2 with anlotinib presents a promising therapeutic strategy for esophageal cancer intervention.
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