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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...

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Autores principales: Menbari, Mohammad-Nazir, Rahimi, Karim, Ahmadi, Abbas, Mohammadi-Yeganeh, Samira, Elyasi, Anvar, Darvishi, Nikoo, Hosseini, Vahedeh, Abdi, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute of Iran 2020
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.
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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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