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Association of HDAC8 Expression with Pathological Findings in Triple Negative and Non-Triple Negative Breast Cancer: Implications for Diagnosis
BACKGROUND: Previous data have shown the tumorigenicity roles of HDAC8 in breast cancer. More recently, the oncogenic effects of this molecule have been revealed in TNBC. The present study aimed to determine the diagnostic value of HDAC8 for the differentiation of TNBC from nTNBC tumors. METHODS: A...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pasteur Institute of Iran
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392136/ https://www.ncbi.nlm.nih.gov/pubmed/32429642 http://dx.doi.org/10.29252/ibj.24.5.283 |
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author | Menbari, Mohammad-Nazir Rahimi, Karim Ahmadi, Abbas Mohammadi-Yeganeh, Samira Elyasi, Anvar Darvishi, Nikoo Hosseini, Vahedeh Abdi, Mohammad |
author_facet | Menbari, Mohammad-Nazir Rahimi, Karim Ahmadi, Abbas Mohammadi-Yeganeh, Samira Elyasi, Anvar Darvishi, Nikoo Hosseini, Vahedeh Abdi, Mohammad |
author_sort | Menbari, Mohammad-Nazir |
collection | PubMed |
description | BACKGROUND: Previous data have shown the tumorigenicity roles of HDAC8 in breast cancer. More recently, the oncogenic effects of this molecule have been revealed in TNBC. The present study aimed to determine the diagnostic value of HDAC8 for the differentiation of TNBC from nTNBC tumors. METHODS: A total of 50 cancerous and normal adjacent tumor specimens were obtained, and the clinical and pathological findings of studied subjects were recorded. The expression of HDAC8 gene was determined by qRT-PCR. Also, immunohistochemical staining was performed on tissue samples. RESULTS: Our results showed that the expression of HDAC8 in breast cancer tissues was significantly higher than the normal adjacent tissues (p = 0.0011). HDAC8 expression was also observed to be higher in TNBC patients than nTNBC group (p = 0.0013). In addition, in the TNBC group, there was a significant association between the HDAC8 overexpression and tumor characteristics, including tumor size (p = 0.039), lymphatic invasion (p = 0.01), tumor grade (p = 0.02), and perineural invasion (p < 0.05). The cut-off value was fixed at 0.6279 r.u., and the corresponding sensitivity and specificity were found to be 73.91% and 70.37%, respectively. CONCLUSION: According to the findings, among the other markers, HDAC8 oncogene may be used as a potential tumor marker in diagnosis of TNBC tumors. |
format | Online Article Text |
id | pubmed-7392136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Pasteur Institute of Iran |
record_format | MEDLINE/PubMed |
spelling | pubmed-73921362020-09-01 Association of HDAC8 Expression with Pathological Findings in Triple Negative and Non-Triple Negative Breast Cancer: Implications for Diagnosis Menbari, Mohammad-Nazir Rahimi, Karim Ahmadi, Abbas Mohammadi-Yeganeh, Samira Elyasi, Anvar Darvishi, Nikoo Hosseini, Vahedeh Abdi, Mohammad Iran Biomed J Full Length BACKGROUND: Previous data have shown the tumorigenicity roles of HDAC8 in breast cancer. More recently, the oncogenic effects of this molecule have been revealed in TNBC. The present study aimed to determine the diagnostic value of HDAC8 for the differentiation of TNBC from nTNBC tumors. METHODS: A total of 50 cancerous and normal adjacent tumor specimens were obtained, and the clinical and pathological findings of studied subjects were recorded. The expression of HDAC8 gene was determined by qRT-PCR. Also, immunohistochemical staining was performed on tissue samples. RESULTS: Our results showed that the expression of HDAC8 in breast cancer tissues was significantly higher than the normal adjacent tissues (p = 0.0011). HDAC8 expression was also observed to be higher in TNBC patients than nTNBC group (p = 0.0013). In addition, in the TNBC group, there was a significant association between the HDAC8 overexpression and tumor characteristics, including tumor size (p = 0.039), lymphatic invasion (p = 0.01), tumor grade (p = 0.02), and perineural invasion (p < 0.05). The cut-off value was fixed at 0.6279 r.u., and the corresponding sensitivity and specificity were found to be 73.91% and 70.37%, respectively. CONCLUSION: According to the findings, among the other markers, HDAC8 oncogene may be used as a potential tumor marker in diagnosis of TNBC tumors. Pasteur Institute of Iran 2020-09 2020-05-02 /pmc/articles/PMC7392136/ /pubmed/32429642 http://dx.doi.org/10.29252/ibj.24.5.283 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Length Menbari, Mohammad-Nazir Rahimi, Karim Ahmadi, Abbas Mohammadi-Yeganeh, Samira Elyasi, Anvar Darvishi, Nikoo Hosseini, Vahedeh Abdi, Mohammad Association of HDAC8 Expression with Pathological Findings in Triple Negative and Non-Triple Negative Breast Cancer: Implications for Diagnosis |
title | Association of HDAC8 Expression with Pathological Findings in Triple Negative and Non-Triple Negative Breast Cancer: Implications for Diagnosis |
title_full | Association of HDAC8 Expression with Pathological Findings in Triple Negative and Non-Triple Negative Breast Cancer: Implications for Diagnosis |
title_fullStr | Association of HDAC8 Expression with Pathological Findings in Triple Negative and Non-Triple Negative Breast Cancer: Implications for Diagnosis |
title_full_unstemmed | Association of HDAC8 Expression with Pathological Findings in Triple Negative and Non-Triple Negative Breast Cancer: Implications for Diagnosis |
title_short | Association of HDAC8 Expression with Pathological Findings in Triple Negative and Non-Triple Negative Breast Cancer: Implications for Diagnosis |
title_sort | association of hdac8 expression with pathological findings in triple negative and non-triple negative breast cancer: implications for diagnosis |
topic | Full Length |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392136/ https://www.ncbi.nlm.nih.gov/pubmed/32429642 http://dx.doi.org/10.29252/ibj.24.5.283 |
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