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Glypican-1 Overexpression in Different Types of Breast Cancers
PURPOSE: Treatment of metastatic breast cancer patients is challenging and remains a major underlying cause of female mortality. Understanding molecular alterations in tumor development is critical to identify novel biomarkers and targets for cancer diagnosis and therapy. One of the aberrant cancer...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8334627/ https://www.ncbi.nlm.nih.gov/pubmed/34366675 http://dx.doi.org/10.2147/OTT.S315200 |
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author | Alshammari, Fatemah O F O Al-Saraireh, Yousef M Youssef, Ahmed M M AL-sarayra, Yahya M Alrawashdeh, Hamzeh Mohammad |
author_facet | Alshammari, Fatemah O F O Al-Saraireh, Yousef M Youssef, Ahmed M M AL-sarayra, Yahya M Alrawashdeh, Hamzeh Mohammad |
author_sort | Alshammari, Fatemah O F O |
collection | PubMed |
description | PURPOSE: Treatment of metastatic breast cancer patients is challenging and remains a major underlying cause of female mortality. Understanding molecular alterations in tumor development is critical to identify novel biomarkers and targets for cancer diagnosis and therapy. One of the aberrant cancer expressions gaining recent research interest is glypican-1. Several studies reported strong glypican-1 expression in various types of human cancers. However, none of these investigated glypican-1 expression in a large cohort of breast cancer histopathological subtypes. PATIENTS AND METHODS: Immunohistochemistry was used to assess glypican-1 expression in 220 breast cancer patients and its relation to demographic and clinical features, as well as important prognostic immunohistochemical markers for breast cancer. RESULTS: Intense glypican-1 expression was recognized in all breast cancer histopathological subtypes. Normal, healthy breast tissue displayed a heterogeneous low expression (20%). Importantly, a strong differential in glypican-1 expression was determined between normal and malignant breast tissues. Moreover, there was a significantly high rate of glypican-1 expression in advanced grades of breast cancer patients and larger tumor sizes. Unfortunately, the glypican-1 expression demonstrated no obvious relationship with the expression of various biomarkers in breast cancer. CONCLUSION: This study may establish glypican-1 as a promising new therapeutic target for the development of therapy in breast cancer. |
format | Online Article Text |
id | pubmed-8334627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-83346272021-08-05 Glypican-1 Overexpression in Different Types of Breast Cancers Alshammari, Fatemah O F O Al-Saraireh, Yousef M Youssef, Ahmed M M AL-sarayra, Yahya M Alrawashdeh, Hamzeh Mohammad Onco Targets Ther Original Research PURPOSE: Treatment of metastatic breast cancer patients is challenging and remains a major underlying cause of female mortality. Understanding molecular alterations in tumor development is critical to identify novel biomarkers and targets for cancer diagnosis and therapy. One of the aberrant cancer expressions gaining recent research interest is glypican-1. Several studies reported strong glypican-1 expression in various types of human cancers. However, none of these investigated glypican-1 expression in a large cohort of breast cancer histopathological subtypes. PATIENTS AND METHODS: Immunohistochemistry was used to assess glypican-1 expression in 220 breast cancer patients and its relation to demographic and clinical features, as well as important prognostic immunohistochemical markers for breast cancer. RESULTS: Intense glypican-1 expression was recognized in all breast cancer histopathological subtypes. Normal, healthy breast tissue displayed a heterogeneous low expression (20%). Importantly, a strong differential in glypican-1 expression was determined between normal and malignant breast tissues. Moreover, there was a significantly high rate of glypican-1 expression in advanced grades of breast cancer patients and larger tumor sizes. Unfortunately, the glypican-1 expression demonstrated no obvious relationship with the expression of various biomarkers in breast cancer. CONCLUSION: This study may establish glypican-1 as a promising new therapeutic target for the development of therapy in breast cancer. Dove 2021-07-30 /pmc/articles/PMC8334627/ /pubmed/34366675 http://dx.doi.org/10.2147/OTT.S315200 Text en © 2021 Alshammari et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Alshammari, Fatemah O F O Al-Saraireh, Yousef M Youssef, Ahmed M M AL-sarayra, Yahya M Alrawashdeh, Hamzeh Mohammad Glypican-1 Overexpression in Different Types of Breast Cancers |
title | Glypican-1 Overexpression in Different Types of Breast Cancers |
title_full | Glypican-1 Overexpression in Different Types of Breast Cancers |
title_fullStr | Glypican-1 Overexpression in Different Types of Breast Cancers |
title_full_unstemmed | Glypican-1 Overexpression in Different Types of Breast Cancers |
title_short | Glypican-1 Overexpression in Different Types of Breast Cancers |
title_sort | glypican-1 overexpression in different types of breast cancers |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8334627/ https://www.ncbi.nlm.nih.gov/pubmed/34366675 http://dx.doi.org/10.2147/OTT.S315200 |
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