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VEGF: A critical driver for angiogenesis and subsequent tumor growth: An IHC study

BACKGROUND: Tumors require blood supply for their growth and dissemination. It is a well accepted paradigm that tumors recruit new blood vessels from the existing circulation (angiogenesis) and this participates in tumor invasion and metastasis. Studies in the literature provide evidence for express...

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Autores principales: Kapoor, Prakhar, Deshmukh, RS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519203/
https://www.ncbi.nlm.nih.gov/pubmed/23248460
http://dx.doi.org/10.4103/0973-029X.102478
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author Kapoor, Prakhar
Deshmukh, RS
author_facet Kapoor, Prakhar
Deshmukh, RS
author_sort Kapoor, Prakhar
collection PubMed
description BACKGROUND: Tumors require blood supply for their growth and dissemination. It is a well accepted paradigm that tumors recruit new blood vessels from the existing circulation (angiogenesis) and this participates in tumor invasion and metastasis. Studies in the literature provide evidence for expression of Vascular Endothelial Growth Factor (VEGF) by the tumor for neo-angiogenesis, which is not only required for the tumor growth but also its metastasis. Based on the literary evidences we carried out an Immuno-Histochemical (IHC) study for VEGF in Oral Squamous Cell Carcinoma (OSCC) tissues to provide a strong link between the factor and oral cancer. AIM: To analyze the expression of VEGF in OSCC tissues of different histological grades, clinical sizes and lymph node status and to use this as an indicator for disease progression by helping in delineating a risk population, that may benefit from an attractive adjuvant therapeutic strategy for OSCC. SETTINGS AND DESIGN: Studies published from 1990 till 2010 have only seen the association of VEGF with tumor angiogenesis and its possible role in metastasis. This is the first study that takes into account the clinical status of the lymph nodes and VEGF expressivity in a sample size of 30 cases. MATERIALS AND METHODS: 30 oral squamous cell carcinoma tissue slides were stained using Hematoxylin and Eosin stain (to confirm the diagnosis) and immunohistochemically using VEGF antibody. IHC stained slides were thereafter evaluated for the positivity and intensity. STATISTICAL ANALYSIS: The result was subjected to statistical analysis using Chi-square test RESULTS AND CONCLUSION: VEGF positivity was seen in approximately. 90% of cases which was independent of histological grade of OSCC. However the intensity increased with the clinical size of cancer and from palpable lymph node to a tender and hard lymph node.
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spelling pubmed-35192032012-12-17 VEGF: A critical driver for angiogenesis and subsequent tumor growth: An IHC study Kapoor, Prakhar Deshmukh, RS J Oral Maxillofac Pathol Original Article BACKGROUND: Tumors require blood supply for their growth and dissemination. It is a well accepted paradigm that tumors recruit new blood vessels from the existing circulation (angiogenesis) and this participates in tumor invasion and metastasis. Studies in the literature provide evidence for expression of Vascular Endothelial Growth Factor (VEGF) by the tumor for neo-angiogenesis, which is not only required for the tumor growth but also its metastasis. Based on the literary evidences we carried out an Immuno-Histochemical (IHC) study for VEGF in Oral Squamous Cell Carcinoma (OSCC) tissues to provide a strong link between the factor and oral cancer. AIM: To analyze the expression of VEGF in OSCC tissues of different histological grades, clinical sizes and lymph node status and to use this as an indicator for disease progression by helping in delineating a risk population, that may benefit from an attractive adjuvant therapeutic strategy for OSCC. SETTINGS AND DESIGN: Studies published from 1990 till 2010 have only seen the association of VEGF with tumor angiogenesis and its possible role in metastasis. This is the first study that takes into account the clinical status of the lymph nodes and VEGF expressivity in a sample size of 30 cases. MATERIALS AND METHODS: 30 oral squamous cell carcinoma tissue slides were stained using Hematoxylin and Eosin stain (to confirm the diagnosis) and immunohistochemically using VEGF antibody. IHC stained slides were thereafter evaluated for the positivity and intensity. STATISTICAL ANALYSIS: The result was subjected to statistical analysis using Chi-square test RESULTS AND CONCLUSION: VEGF positivity was seen in approximately. 90% of cases which was independent of histological grade of OSCC. However the intensity increased with the clinical size of cancer and from palpable lymph node to a tender and hard lymph node. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3519203/ /pubmed/23248460 http://dx.doi.org/10.4103/0973-029X.102478 Text en Copyright: © Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kapoor, Prakhar
Deshmukh, RS
VEGF: A critical driver for angiogenesis and subsequent tumor growth: An IHC study
title VEGF: A critical driver for angiogenesis and subsequent tumor growth: An IHC study
title_full VEGF: A critical driver for angiogenesis and subsequent tumor growth: An IHC study
title_fullStr VEGF: A critical driver for angiogenesis and subsequent tumor growth: An IHC study
title_full_unstemmed VEGF: A critical driver for angiogenesis and subsequent tumor growth: An IHC study
title_short VEGF: A critical driver for angiogenesis and subsequent tumor growth: An IHC study
title_sort vegf: a critical driver for angiogenesis and subsequent tumor growth: an ihc study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519203/
https://www.ncbi.nlm.nih.gov/pubmed/23248460
http://dx.doi.org/10.4103/0973-029X.102478
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