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The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer

BACKGROUND: Breast cancer is the most common malignancy in women world-wide. Triple negative breast cancer (TNBC) is a highly aggressive subtype that lacks expression of hormone receptors for estrogen, progesterone and human epidermal growth factor 2; and is associated with a high propensity for met...

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Autores principales: Avery-Kiejda, Kelly A, Braye, Stephen G, Forbes, John F, Scott, Rodney J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021460/
https://www.ncbi.nlm.nih.gov/pubmed/24725360
http://dx.doi.org/10.1186/1471-2407-14-253
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author Avery-Kiejda, Kelly A
Braye, Stephen G
Forbes, John F
Scott, Rodney J
author_facet Avery-Kiejda, Kelly A
Braye, Stephen G
Forbes, John F
Scott, Rodney J
author_sort Avery-Kiejda, Kelly A
collection PubMed
description BACKGROUND: Breast cancer is the most common malignancy in women world-wide. Triple negative breast cancer (TNBC) is a highly aggressive subtype that lacks expression of hormone receptors for estrogen, progesterone and human epidermal growth factor 2; and is associated with a high propensity for metastatic spread. Several studies have identified critical roles for microRNAs in breast cancer, but the role of two critical enzymes involved in microRNA biogenesis, Dicer and Drosha, is not well understood, particularly with respect to metastatic progression in this subtype. METHODS: We examined the expression of Dicer and Drosha in a series of invasive 35 TNBCs with matched normal adjacent tissues (n = 18) and lymph node metastases (n = 15) using semi-quantitative real time RT-PCR. The relationship of their expression with clinical features including age at diagnosis, lymph node positivity and tumour size was analysed. RESULTS: We report that Dicer was significantly decreased while Drosha was significantly increased in tumours when compared to normal adjacent tissues. While there was no difference in Drosha expression in lymph node metastases when compared to the primary tumour, Dicer was significantly increased. There was no correlation between the expression of either Dicer or Drosha to age at diagnosis, lymph node positivity and tumour size. CONCLUSIONS: In conclusion, Dicer and Drosha are dysregulated in TNBC and matched lymph node metastases however, the clinical relevance of this is still not known. The altered expression of Dicer and Drosha may serve as markers for disrupted miRNA biogenesis in TNBC.
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spelling pubmed-40214602014-05-16 The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer Avery-Kiejda, Kelly A Braye, Stephen G Forbes, John F Scott, Rodney J BMC Cancer Research Article BACKGROUND: Breast cancer is the most common malignancy in women world-wide. Triple negative breast cancer (TNBC) is a highly aggressive subtype that lacks expression of hormone receptors for estrogen, progesterone and human epidermal growth factor 2; and is associated with a high propensity for metastatic spread. Several studies have identified critical roles for microRNAs in breast cancer, but the role of two critical enzymes involved in microRNA biogenesis, Dicer and Drosha, is not well understood, particularly with respect to metastatic progression in this subtype. METHODS: We examined the expression of Dicer and Drosha in a series of invasive 35 TNBCs with matched normal adjacent tissues (n = 18) and lymph node metastases (n = 15) using semi-quantitative real time RT-PCR. The relationship of their expression with clinical features including age at diagnosis, lymph node positivity and tumour size was analysed. RESULTS: We report that Dicer was significantly decreased while Drosha was significantly increased in tumours when compared to normal adjacent tissues. While there was no difference in Drosha expression in lymph node metastases when compared to the primary tumour, Dicer was significantly increased. There was no correlation between the expression of either Dicer or Drosha to age at diagnosis, lymph node positivity and tumour size. CONCLUSIONS: In conclusion, Dicer and Drosha are dysregulated in TNBC and matched lymph node metastases however, the clinical relevance of this is still not known. The altered expression of Dicer and Drosha may serve as markers for disrupted miRNA biogenesis in TNBC. BioMed Central 2014-04-11 /pmc/articles/PMC4021460/ /pubmed/24725360 http://dx.doi.org/10.1186/1471-2407-14-253 Text en Copyright © 2014 Avery-Kiejda et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Avery-Kiejda, Kelly A
Braye, Stephen G
Forbes, John F
Scott, Rodney J
The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer
title The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer
title_full The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer
title_fullStr The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer
title_full_unstemmed The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer
title_short The expression of Dicer and Drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer
title_sort expression of dicer and drosha in matched normal tissues, tumours and lymph node metastases in triple negative breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021460/
https://www.ncbi.nlm.nih.gov/pubmed/24725360
http://dx.doi.org/10.1186/1471-2407-14-253
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