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Relationship of angiogenic and apoptotic activities in soft-tissue sarcoma
INTRODUCTION: Angiogenesis and apoptosis play an essential role in tumor development and progression. Previous studies on apoptosis and angiogenesis of soft-tissue sarcoma (STS) were done separately. This is the first study of the relationship between apoptotic and angiogenic activity. Correlation o...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134609/ https://www.ncbi.nlm.nih.gov/pubmed/25136525 http://dx.doi.org/10.4103/2278-330X.136799 |
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author | Win, Thin Thin Jaafar, Hasnan Yusuf, Yusri |
author_facet | Win, Thin Thin Jaafar, Hasnan Yusuf, Yusri |
author_sort | Win, Thin Thin |
collection | PubMed |
description | INTRODUCTION: Angiogenesis and apoptosis play an essential role in tumor development and progression. Previous studies on apoptosis and angiogenesis of soft-tissue sarcoma (STS) were done separately. This is the first study of the relationship between apoptotic and angiogenic activity. Correlation of expression of anti-apoptotic protein (Bcl-2) and pro-apoptotic protein (Bax) in the tumor cells (TCs) with their expression in endothelial cell (EC) of the tumor blood vessels in STS were also carried out. MATERIALS AND METHODS: 101 cases of STS; consisting liposarcoma, malignant fibrous histiocytoma, synovial sarcoma, fibrosarcoma, leiomyosarcoma, rhabdomyosarcoma and malignant peripheral nerve sheath tumor; were collected and immunohistochemical reaction of vascular endothelial growth factor (VEGF), Bcl-2 and Bax were examined. RESULTS: Higher Bax expression in TCs (54.5%) was seen compared to Bcl-2 expression (44.6%). There was a significant association between Bcl-2 and Bax in TCs with ECs. Significant association was also seen between histological types of STS with Bcl-2 expression; however not with Bax expression. There was an association between VEGF and Bax with high VEGF expression and weak Bax expression. However, VEGF expression was not associated with Bcl-2 expression and histological types. CONCLUSION: This study supports the role of ECs of tumor blood vessels and apoptosis of TCs in tumor management. Increased angiogenesis may inhibit apoptosis of TCs and lead to tumor growth. Therefore, inhibition of ECs survival or activation of ECs death is promising prospect for tumor therapy. Immunohistochemical antibodies in this study might be potential useful marker for the prognosis of STS. |
format | Online Article Text |
id | pubmed-4134609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41346092014-08-18 Relationship of angiogenic and apoptotic activities in soft-tissue sarcoma Win, Thin Thin Jaafar, Hasnan Yusuf, Yusri South Asian J Cancer SOFT TISSUE SARCOMA: Original Article INTRODUCTION: Angiogenesis and apoptosis play an essential role in tumor development and progression. Previous studies on apoptosis and angiogenesis of soft-tissue sarcoma (STS) were done separately. This is the first study of the relationship between apoptotic and angiogenic activity. Correlation of expression of anti-apoptotic protein (Bcl-2) and pro-apoptotic protein (Bax) in the tumor cells (TCs) with their expression in endothelial cell (EC) of the tumor blood vessels in STS were also carried out. MATERIALS AND METHODS: 101 cases of STS; consisting liposarcoma, malignant fibrous histiocytoma, synovial sarcoma, fibrosarcoma, leiomyosarcoma, rhabdomyosarcoma and malignant peripheral nerve sheath tumor; were collected and immunohistochemical reaction of vascular endothelial growth factor (VEGF), Bcl-2 and Bax were examined. RESULTS: Higher Bax expression in TCs (54.5%) was seen compared to Bcl-2 expression (44.6%). There was a significant association between Bcl-2 and Bax in TCs with ECs. Significant association was also seen between histological types of STS with Bcl-2 expression; however not with Bax expression. There was an association between VEGF and Bax with high VEGF expression and weak Bax expression. However, VEGF expression was not associated with Bcl-2 expression and histological types. CONCLUSION: This study supports the role of ECs of tumor blood vessels and apoptosis of TCs in tumor management. Increased angiogenesis may inhibit apoptosis of TCs and lead to tumor growth. Therefore, inhibition of ECs survival or activation of ECs death is promising prospect for tumor therapy. Immunohistochemical antibodies in this study might be potential useful marker for the prognosis of STS. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4134609/ /pubmed/25136525 http://dx.doi.org/10.4103/2278-330X.136799 Text en Copyright: © South Asian Journal of Cancer 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 | SOFT TISSUE SARCOMA: Original Article Win, Thin Thin Jaafar, Hasnan Yusuf, Yusri Relationship of angiogenic and apoptotic activities in soft-tissue sarcoma |
title | Relationship of angiogenic and apoptotic activities in soft-tissue sarcoma |
title_full | Relationship of angiogenic and apoptotic activities in soft-tissue sarcoma |
title_fullStr | Relationship of angiogenic and apoptotic activities in soft-tissue sarcoma |
title_full_unstemmed | Relationship of angiogenic and apoptotic activities in soft-tissue sarcoma |
title_short | Relationship of angiogenic and apoptotic activities in soft-tissue sarcoma |
title_sort | relationship of angiogenic and apoptotic activities in soft-tissue sarcoma |
topic | SOFT TISSUE SARCOMA: Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4134609/ https://www.ncbi.nlm.nih.gov/pubmed/25136525 http://dx.doi.org/10.4103/2278-330X.136799 |
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