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Updated: Jun 15, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Inhibiting colorectal carcinoma growth and metastasis by blocking the expression of VEGF using RNA interference
Shaochuang Wang1, Hui Liu, Lifeng Ren
1National Hepatobiliary and Enteric Surgery Research Center, Ministry of Health, Central South University, Hunan Province, 410008, People's Republic of China.
Abstract:
Angiogenesis plays an essential role in tumor growth and metastasis and is a promising target for cancer therapy. Vascular endothelial growth factor (VEGF) is a key regulator of angiogenesis. The present study was designed to determine the role of VEGF in tumor growth and metastasis using RNA interference (RNAi) technology. Four small interfering RNA (siRNA) sequences for the VEGF gene were cloned into expression plasmids and transfected into human colorectal carcinoma (CRC) SW620 cells. Stable transfection of these plasmids decreased VEGF protein expression, leading to the potent suppression of tumor cell proliferation, migration, invasion, and angiogenesis in vitro. Furthermore, in subcutaneous and intrasplenic/portal injection models involving athymic nude mice, the tumor growth and metastasis of SW620 cells expressing VEGF siRNA were significantly inhibited compared with untransfected cells or cells transfected with control vector alone. Immunohistochemical analyses of tumor sections revealed a decreased vessel density and decreased VEGF expression in the animals where siRNA against VEGF were expressed. These results indicate that RNAi of VEGF can be an effective antiangiogenic strategy for CRC.
Insights
RNA interference targeting vascular endothelial growth factor (VEGF) effectively suppressed colorectal cancer cell growth and metastasis in preclinical models. This anti-angiogenic strategy shows promise for treating this common cancer type.
Area of Science:
- Oncology
- Molecular Biology
- Biotechnology
Background:
- Angiogenesis is crucial for tumor progression and metastasis, making it a key therapeutic target.
- Vascular endothelial growth factor (VEGF) is a primary regulator of angiogenesis.
- RNA interference (RNAi) offers a potential method to target VEGF-driven tumor growth.
Purpose of the Study:
- To investigate the role of VEGF in colorectal carcinoma (CRC) tumor growth and metastasis.
- To evaluate the efficacy of RNA interference (RNAi) targeting VEGF using small interfering RNA (siRNA).
Main Methods:
- Four VEGF-specific siRNA sequences were designed and cloned into expression plasmids.
- Human colorectal carcinoma (CRC) SW620 cells were stably transfected with these plasmids.
- Tumorigenicity and metastasis were assessed in vitro and in athymic nude mouse models.
Main Results:
- Stable transfection significantly reduced VEGF protein expression in SW620 cells.
- VEGF siRNA suppressed tumor cell proliferation, migration, invasion, and angiogenesis in vitro.
- Tumor growth and metastasis were significantly inhibited in mice receiving VEGF siRNA-expressing cells.
- Immunohistochemistry confirmed reduced vessel density and VEGF expression in tumors.
Conclusions:
- RNA interference targeting VEGF is a potent strategy for inhibiting colorectal cancer growth and metastasis.
- This anti-angiogenic approach holds significant therapeutic potential for colorectal cancer treatment.
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This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
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This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
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