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Updated: Aug 24, 2026

A Simple Bioassay for the Evaluation of Vascular Endothelial Growth Factors
Published on: March 15, 2016
A small interfering RNA targeting vascular endothelial growth factor as cancer therapeutics
Yoshifumi Takei1, Kenji Kadomatsu, Yukio Yuzawa
1Department of Biochemistry, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Japan. takei@med.nagoya-u.ac.jp
Abstract:
Vascular endothelial growth factor (VEGF) plays a critical role during normal embryonic angiogenesis and also in the pathological angiogenesis that occurs in a number of diseases, including cancer. We developed a novel VEGF blockade system using RNA interference. The small interfering RNA (siRNA) targeting human VEGF almost completely inhibited the secretion of VEGF in a human prostate cancer cell line, PC-3, whereas the control scramble siRNA showed no effects. The VEGF siRNA with atelocollagen dramatically suppressed tumor angiogenesis and tumor growth in a PC-3 s.c. xenograft model. Atelocollagen provided a beneficial delivering means by which stabilization and efficient transfection of the siRNA injected into the tumors were achieved.
Insights
This study introduces a novel RNA interference system to block vascular endothelial growth factor (VEGF) in prostate cancer. The developed VEGF small interfering RNA (siRNA) effectively inhibited tumor growth and angiogenesis in preclinical models.
Area of Science:
- Oncology
- Molecular Biology
- Biotechnology
Background:
- Vascular endothelial growth factor (VEGF) is crucial for angiogenesis in development and diseases like cancer.
- Pathological angiogenesis contributes to tumor growth and metastasis.
Purpose of the Study:
- To develop and evaluate a novel RNA interference (RNAi) system for blocking VEGF.
- To assess the efficacy of VEGF-targeting small interfering RNA (siRNA) in a prostate cancer model.
Main Methods:
- Developed siRNA targeting human VEGF.
- Tested siRNA efficacy in PC-3 prostate cancer cells in vitro.
- Evaluated VEGF siRNA with atelocollagen in a PC-3 subcutaneous xenograft mouse model.
Main Results:
- VEGF siRNA significantly inhibited VEGF secretion in PC-3 cells.
- The combination of VEGF siRNA and atelocollagen suppressed tumor angiogenesis and growth.
- Atelocollagen facilitated siRNA stabilization and efficient transfection in tumors.
Conclusions:
- RNA interference targeting VEGF is a promising strategy for prostate cancer therapy.
- Atelocollagen serves as an effective delivery vehicle for VEGF siRNA, enhancing therapeutic outcomes.
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