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TFF1 antagonizes TIMP-1 mediated proliferative functions in gastric cancer
Omar M Omar1, Mohammed Soutto2,3, Nadeem S Bhat3
1Department of Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.
Abstract:
Tissue inhibitor matrix metalloproteinase-1 (TIMP1) is one of four identified members of the TIMP family. We evaluated the role of TIMP1 in gastric cancer using human and mouse tissues along with gastric organoids and in vitro cell models. Using quantitative real-time RT-PCR, we detected significant overexpression of TIMP1 in the human gastric cancer samples, as compared to normal stomach samples (P < 0.01). We also detected overexpression of Timp1 in neoplastic gastric lesions of the Tff1-knockout (KO) mice, as compared to normal stomach tissues. Reconstitution of TFF1 in human gastric cancer cell lines led to a significant decrease in the mRNA expression level of TIMP1 (P < 0.05). In vitro analysis demonstrated that TIMP1 mRNA expression is induced by TNF-α and activation of NF-κB whereas inhibition of NF-κB using BAY11-7082 led to inhibition of NF-κB and downregulation of TIMP1. Western blot analysis confirmed the decrease in TIMP1 protein level following reconstitution of TFF1. By using immunofluorescence, we showed nuclear localization of NF-κB and expression of TIMP1 in gastric organoids established from the Tff1-KO stomach where reconstitution of Tff1 using recombinant protein led to a notable reduction in the expression of both NF-κB and TIMP1. Using EDU assay, as a measure of proliferating cells, we found that TIMP1 promotes cellular proliferation whereas TFF1 reconstitution leads to a significant decrease in cellular proliferation (P < 0.05). In summary, our findings demonstrate overexpression of TIMP1 in mouse and human gastric cancers through NF-kB-dependent mechanism. We also show that TFF1 suppresses NF-κB and inhibits TIMP1-mediated proliferative potential in gastric cancer.
Insights
Tissue inhibitor of metalloproteinase-1 (TIMP1) is overexpressed in gastric cancer, promoting proliferation. TFF1 suppresses NF-κB, reducing TIMP1 levels and proliferation in gastric cancer models.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Tissue inhibitor of metalloproteinase-1 (TIMP1) is a key regulator of extracellular matrix degradation.
- Gastric cancer remains a significant global health challenge with complex underlying molecular mechanisms.
- The role of TIMP1 in gastric tumorigenesis requires further elucidation.
Purpose of the Study:
- To investigate the role of TIMP1 in gastric cancer development and progression.
- To explore the regulatory mechanisms of TIMP1 expression in gastric cancer.
- To assess the potential of TFF1 as a suppressor of gastric cancer proliferation.
Main Methods:
- Quantitative real-time RT-PCR and Western blot analysis for TIMP1 expression.
- In vitro cell models and gastric organoids derived from Tff1-knockout mice.
- NF-κB activation/inhibition assays and immunofluorescence.
- EDU assay to measure cellular proliferation.
Main Results:
- TIMP1 was significantly overexpressed in human gastric cancer tissues and Tff1-knockout mouse gastric lesions.
- TIMP1 expression is induced by TNF-α via NF-κB activation.
- TFF1 reconstitution decreased TIMP1 expression and NF-κB activity.
- TIMP1 promoted cellular proliferation, while TFF1 suppressed it.
Conclusions:
- TIMP1 is overexpressed in gastric cancer through an NF-κB-dependent mechanism.
- TFF1 acts as a suppressor by inhibiting NF-κB and reducing TIMP1-mediated proliferation.
- Targeting TIMP1 and modulating TFF1 could offer therapeutic strategies for gastric cancer.
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