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Updated: Jun 18, 2026

DNA Vector-based RNA Interference to Study Gene Function in Cancer
Published on: June 4, 2012
Inhibiting tumor growth of colorectal cancer by blocking the expression of vascular endothelial growth factor
Zhicheng Lui1, Qiang Ma, Xianghui Wang
1Department of General Surgery, Lanzhou University Second Hospital, Lanzhou 730030, P.R. China.
Abstract:
Many reports show that vascular endothelial growth factor receptor 3 (VEGFR3) plays an essential role in tumor metastasis and is a promising target for cancer therapy. The present study was designed to determine the role of VEGFR3 in tumor growth using RNA interference (RNAi) technology. Three small interfering RNA (siRNA) sequences for the VEGFR3 gene were cloned into expression plasmids (pSUPER) and transfected into human colorectal carcinoma (CRC) LoVo cells. Stable transfection of these plasmids decreased VEGFR3 protein expression, leading to the potent suppression of tumor cell proliferation and lymphangiogenesis in vitro. Furthermore, we selected the most effective silenced expressor vector and injected it and pSUPER vector into a tumor xenograft model in nude mice. The tumor growth of LoVo cells expressing VEGFR3 siRNA were significantly inhibited compared with cells transfected with control vector alone. Immunohistochemical analyses of tumor sections revealed a decreased vessel density and decreased VEGFR3 expression in animals when siRNA against VEGFR3 was expressed. These results showed that RNAi of VEGFR3 is an effective tool to reduce lymphangiogenesis in CRC.
Insights
RNA interference targeting vascular endothelial growth factor receptor 3 (VEGFR3) effectively suppressed colorectal cancer cell growth and lymphangiogenesis. This study demonstrates VEGFR3 as a viable target for inhibiting tumor metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Biotechnology
Background:
- Vascular endothelial growth factor receptor 3 (VEGFR3) is implicated in tumor metastasis.
- VEGFR3 presents a promising therapeutic target for cancer treatment.
Purpose of the Study:
- To investigate the role of VEGFR3 in tumor growth using RNA interference (RNAi).
- To evaluate the efficacy of VEGFR3 inhibition in colorectal carcinoma (CRC).
Main Methods:
- Three small interfering RNA (siRNA) sequences targeting VEGFR3 were designed and cloned into expression plasmids.
- Human colorectal carcinoma (CRC) LoVo cells were stably transfected with VEGFR3 siRNA.
- Tumorigenicity and lymphangiogenesis were assessed in vitro and in a tumor xenograft model in nude mice.
Main Results:
- Stable transfection of VEGFR3 siRNA significantly reduced VEGFR3 protein expression in LoVo cells.
- VEGFR3 inhibition potently suppressed tumor cell proliferation and lymphangiogenesis in vitro.
- Tumor growth was significantly inhibited in mice bearing LoVo cells with VEGFR3 siRNA compared to controls.
- Immunohistochemical analysis showed decreased vessel density and VEGFR3 expression in tumors.
Conclusions:
- RNAi-mediated silencing of VEGFR3 is an effective strategy to inhibit colorectal cancer growth.
- Targeting VEGFR3 reduces tumor-associated lymphangiogenesis, offering a potential therapeutic approach for CRC metastasis.
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