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The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1

BACKGROUND: Angiogenesis is an important biological process involved in the proliferation of endothelial cells, tumor growth and metastasis. Vascular endothelial growth factor (VEGF) is considered as a prominent regulator of angiogenesis which exerts the aforementioned effect(s) through its respecti...

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Autores principales: Jafari Sani, Moslem, Yazdi, Foad, Masoomi Karimi, Masoomeh, Alizadeh, Javad, Rahmati, Majid, Zarei Mahmudabadi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893410/
https://www.ncbi.nlm.nih.gov/pubmed/27275397
http://dx.doi.org/10.5812/ircmj.23418
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author Jafari Sani, Moslem
Yazdi, Foad
Masoomi Karimi, Masoomeh
Alizadeh, Javad
Rahmati, Majid
Zarei Mahmudabadi, Ali
author_facet Jafari Sani, Moslem
Yazdi, Foad
Masoomi Karimi, Masoomeh
Alizadeh, Javad
Rahmati, Majid
Zarei Mahmudabadi, Ali
author_sort Jafari Sani, Moslem
collection PubMed
description BACKGROUND: Angiogenesis is an important biological process involved in the proliferation of endothelial cells, tumor growth and metastasis. Vascular endothelial growth factor (VEGF) is considered as a prominent regulator of angiogenesis which exerts the aforementioned effect(s) through its respective receptors (VEGFR1 and VEGFR2). VEGF receptors are targeted as a therapeutic candidate for cancer growth inhibition. RNAi as a new and promising strategy has provided a useful means to specifically suppress gene expression in cancer cells. OBJECTIVES: The current study aimed to down-regulate expression of the VEGFR1 using siRNA. MATERIALS AND METHODS: This experimental study designed specific siRNAs against VEGFR1. Total RNA was extracted from human umbilical vain endothelial cell (HUVEC) and subsequently cDNA was synthetized. PCR was performed using specific primers to amplify the target gene. After double digestion and purification, the gene was cloned into pEFGP-N1 expression vector. Then, AGS cells were transfected with recombinant pEGFP-N1 using lipofectamin. The gene expression and down-regulation were evaluated by fluorescence scanning, reverse transcription PCR (RT-PCR) and Western blot techniques. RESULTS: Fluorescent scanning, RT-PCR (27.68%) and western blot analysis (31.06%) showed that the expression of VEGFR1 was suppressed effectively. CONCLUSIONS: The results of the current study showed that specifically designed siRNA can be considered as an appropriate strategy to suppress gene expression and might be a promising tool to prevent angiogenesis.
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spelling pubmed-48934102016-06-06 The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1 Jafari Sani, Moslem Yazdi, Foad Masoomi Karimi, Masoomeh Alizadeh, Javad Rahmati, Majid Zarei Mahmudabadi, Ali Iran Red Crescent Med J Research Article BACKGROUND: Angiogenesis is an important biological process involved in the proliferation of endothelial cells, tumor growth and metastasis. Vascular endothelial growth factor (VEGF) is considered as a prominent regulator of angiogenesis which exerts the aforementioned effect(s) through its respective receptors (VEGFR1 and VEGFR2). VEGF receptors are targeted as a therapeutic candidate for cancer growth inhibition. RNAi as a new and promising strategy has provided a useful means to specifically suppress gene expression in cancer cells. OBJECTIVES: The current study aimed to down-regulate expression of the VEGFR1 using siRNA. MATERIALS AND METHODS: This experimental study designed specific siRNAs against VEGFR1. Total RNA was extracted from human umbilical vain endothelial cell (HUVEC) and subsequently cDNA was synthetized. PCR was performed using specific primers to amplify the target gene. After double digestion and purification, the gene was cloned into pEFGP-N1 expression vector. Then, AGS cells were transfected with recombinant pEGFP-N1 using lipofectamin. The gene expression and down-regulation were evaluated by fluorescence scanning, reverse transcription PCR (RT-PCR) and Western blot techniques. RESULTS: Fluorescent scanning, RT-PCR (27.68%) and western blot analysis (31.06%) showed that the expression of VEGFR1 was suppressed effectively. CONCLUSIONS: The results of the current study showed that specifically designed siRNA can be considered as an appropriate strategy to suppress gene expression and might be a promising tool to prevent angiogenesis. Kowsar 2016-02-02 /pmc/articles/PMC4893410/ /pubmed/27275397 http://dx.doi.org/10.5812/ircmj.23418 Text en Copyright © 2016, Iranian Red Crescent Medical Journal http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Research Article
Jafari Sani, Moslem
Yazdi, Foad
Masoomi Karimi, Masoomeh
Alizadeh, Javad
Rahmati, Majid
Zarei Mahmudabadi, Ali
The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1
title The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1
title_full The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1
title_fullStr The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1
title_full_unstemmed The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1
title_short The siRNA-Mediated Down-Regulation of Vascular Endothelial Growth Factor Receptor1
title_sort sirna-mediated down-regulation of vascular endothelial growth factor receptor1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4893410/
https://www.ncbi.nlm.nih.gov/pubmed/27275397
http://dx.doi.org/10.5812/ircmj.23418
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