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Effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma

The aim of the present study was to investigate the effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma. A total of 30 nude mice were randomly divided into three groups, namely the control, the Avastin I (Avastin 3 mg/kg) and the Avastin II...

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Autores principales: ZHANG, NALI, ZHANG, GUOJUN, ZHENG, YOUGUANG, WANG, TONGBING, WANG, HONGLEI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217769/
https://www.ncbi.nlm.nih.gov/pubmed/25371722
http://dx.doi.org/10.3892/etm.2014.1991
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author ZHANG, NALI
ZHANG, GUOJUN
ZHENG, YOUGUANG
WANG, TONGBING
WANG, HONGLEI
author_facet ZHANG, NALI
ZHANG, GUOJUN
ZHENG, YOUGUANG
WANG, TONGBING
WANG, HONGLEI
author_sort ZHANG, NALI
collection PubMed
description The aim of the present study was to investigate the effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma. A total of 30 nude mice were randomly divided into three groups, namely the control, the Avastin I (Avastin 3 mg/kg) and the Avastin II (Avastin 6 mg/kg) groups. Following treatment, ELISA was used to detect the expression level of vascular endothelial growth factor (VEGF) in tumor tissues. The microvascular density in tumor tissues and tumor vascular pericyte coverage was detected by immunofluorescence. The tumor growth and survival rate of mice in the three groups were also analyzed. Compared with the control group, the Avastin I and II groups exhibited significantly decreased VEGF levels and microvascular density in the tumor tissues, with the decrease in the Avastin II group being more prominent (P<0.05). After 7 days of treatment, the vascular pericyte coverage in the tumor tissues of mice in the Avastin I and II groups was significantly increased compared with that in the control group mice (P<0.05). Compared with the control group, the mice in the Avastin I and II groups exhibited a significantly decreased tumor growth rate and this effect was dose-dependent. The survival rate of mice in the Avastin I and II groups was significantly increased compared with that of the mice in the control group (P<0.05). In conclusion, Avastin significantly decreased the microvascular density of the tumor in nude mice with A549 lung adenocarcinoma and also significantly increased tumor vascular pericyte coverage, inhibited tumor growth and increased the survival rate of the mice, through its potent antiangiogenic activity.
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spelling pubmed-42177692014-11-04 Effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma ZHANG, NALI ZHANG, GUOJUN ZHENG, YOUGUANG WANG, TONGBING WANG, HONGLEI Exp Ther Med Articles The aim of the present study was to investigate the effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma. A total of 30 nude mice were randomly divided into three groups, namely the control, the Avastin I (Avastin 3 mg/kg) and the Avastin II (Avastin 6 mg/kg) groups. Following treatment, ELISA was used to detect the expression level of vascular endothelial growth factor (VEGF) in tumor tissues. The microvascular density in tumor tissues and tumor vascular pericyte coverage was detected by immunofluorescence. The tumor growth and survival rate of mice in the three groups were also analyzed. Compared with the control group, the Avastin I and II groups exhibited significantly decreased VEGF levels and microvascular density in the tumor tissues, with the decrease in the Avastin II group being more prominent (P<0.05). After 7 days of treatment, the vascular pericyte coverage in the tumor tissues of mice in the Avastin I and II groups was significantly increased compared with that in the control group mice (P<0.05). Compared with the control group, the mice in the Avastin I and II groups exhibited a significantly decreased tumor growth rate and this effect was dose-dependent. The survival rate of mice in the Avastin I and II groups was significantly increased compared with that of the mice in the control group (P<0.05). In conclusion, Avastin significantly decreased the microvascular density of the tumor in nude mice with A549 lung adenocarcinoma and also significantly increased tumor vascular pericyte coverage, inhibited tumor growth and increased the survival rate of the mice, through its potent antiangiogenic activity. D.A. Spandidos 2014-12 2014-09-24 /pmc/articles/PMC4217769/ /pubmed/25371722 http://dx.doi.org/10.3892/etm.2014.1991 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
ZHANG, NALI
ZHANG, GUOJUN
ZHENG, YOUGUANG
WANG, TONGBING
WANG, HONGLEI
Effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma
title Effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma
title_full Effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma
title_fullStr Effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma
title_full_unstemmed Effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma
title_short Effect of Avastin on the number and structure of tumor blood vessels of nude mice with A549 lung adenocarcinoma
title_sort effect of avastin on the number and structure of tumor blood vessels of nude mice with a549 lung adenocarcinoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217769/
https://www.ncbi.nlm.nih.gov/pubmed/25371722
http://dx.doi.org/10.3892/etm.2014.1991
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