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Updated: Mar 12, 2026

In Vitro Assay to Study Tumor-macrophage Interaction
Published on: August 1, 2019
Elevated AEG-1 expression in macrophages promotes hypopharyngeal cancer invasion through the STAT3-MMP-9 signaling
Xiuxiu Liu1,2, Zhenghua Lv1, Jidong Zou1
1Department of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China.
Abstract:
Macrophages play a critical role in tumor invasion and metastasis, which remain major causes of mortality in patients with hypopharyngeal cancer. Here we investigate the effect of an oncogene, AEG-1 expressed in macrophages on the invasion of hypopharyngeal cancer cells. AEG-1 is more highly expressed in macrophages of human hypopharyngeal cancer samples compared with adjacent non-tumor controls. Using matrigel invasion assay system, THP-1-derived macrophages with forced AEG-1 overexpression enhance FaDu cell invasion whereas macrophages with AEG-1 silence inhibit. Matrix metalloproteinase 9 (MMP-9), which is important in tumor invasion and metastasis through degrading extracellular matrix, is up-reulated by AEG-1 partly through NF-κB p65 in macrophages. Intriguingly, macrophage AEG-1 also induces MMP-9 up-regulated expression in FaDu cells. Furthermore, macrophage AEG-1 activates signal transducer and activator of transcription 3 (STAT3) in FaDu cells, which is responsible for macrophage AEG-1-induced an increase in MMP-9 expression and invasion of FaDu cells. This is the first to demonstrate that macrophage AEG-1 promotes tumor invasion through up-regulation of MMP-9 in both macrophages and cancer cells. Thus, the results provide evidences that macrophage AEG-1 contributes to promotion of tumor invasion, and represents as a potential target in hypopharyngeal cancer therapy.
Insights
Oncogene AEG-1 in macrophages promotes hypopharyngeal cancer invasion by up-regulating matrix metalloproteinase 9 (MMP-9). Targeting macrophage AEG-1 may offer a new therapeutic strategy for this cancer.
Area of Science:
- Oncology
- Cancer Biology
- Immunology
Background:
- Macrophages are crucial in tumor invasion and metastasis, leading causes of mortality in hypopharyngeal cancer.
- The role of the oncogene AEG-1 in macrophages concerning hypopharyngeal cancer invasion is not well understood.
Purpose of the Study:
- To investigate the effect of AEG-1 expressed in macrophages on hypopharyngeal cancer cell invasion.
- To elucidate the underlying molecular mechanisms involving MMP-9 and STAT3 signaling.
Main Methods:
- Analysis of AEG-1 expression in human hypopharyngeal cancer tissues.
- Matrigel invasion assays using THP-1-derived macrophages with altered AEG-1 levels (overexpression and silence).
- Investigation of signaling pathways including NF-κB p65 and STAT3.
Main Results:
- AEG-1 is upregulated in macrophages from hypopharyngeal cancer samples.
- Macrophage AEG-1 overexpression enhances FaDu cell invasion, while AEG-1 silence inhibits it.
- AEG-1 up-regulates MMP-9 in macrophages via NF-κB p65 and in FaDu cells via STAT3 activation, promoting cancer cell invasion.
Conclusions:
- Macrophage-derived AEG-1 significantly promotes hypopharyngeal cancer cell invasion.
- AEG-1 enhances invasion by up-regulating MMP-9 in both macrophages and cancer cells.
- Macrophage AEG-1 represents a potential therapeutic target for hypopharyngeal cancer.
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