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The long non coding RNA H19 as a biomarker for breast cancer diagnosis in Lebanese women
Breast cancer is the most common cancer in women worldwide. Minimally invasive percutaneous image-guided biopsies are the current cornerstone in the diagnosis of breast lesions detected on mammography/ultrasonography/MRI or palpable clinically. However, apparently benign breast disease seen on benig...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747713/ https://www.ncbi.nlm.nih.gov/pubmed/33335214 http://dx.doi.org/10.1038/s41598-020-79285-z |
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author | Elias-Rizk, Tamina El Hajj, Joelle Segal-Bendirdjian, Evelyne Hilal, George |
author_facet | Elias-Rizk, Tamina El Hajj, Joelle Segal-Bendirdjian, Evelyne Hilal, George |
author_sort | Elias-Rizk, Tamina |
collection | PubMed |
description | Breast cancer is the most common cancer in women worldwide. Minimally invasive percutaneous image-guided biopsies are the current cornerstone in the diagnosis of breast lesions detected on mammography/ultrasonography/MRI or palpable clinically. However, apparently benign breast disease seen on benign biopsies is a limiting factor for diagnosis and a risk factor of breast cancer especially in the high-risk category patients. Hypothesizing that molecular changes often occur before morphological variations, the levels of the LncRNA H19 were measured in anonymous tissues obtained from 79 women’s image guided breast biopsies, and correlated with cancer progression and aggressiveness. Using a double-blinded approach, H19 might be attributed an interesting role of a more sensitive biomarker in core breast biopsies, independently of the radiological/clinical classification and distant from the clinical management. We established different thresholds for H19 levels in normal versus proliferative, versus malignant tissues. Additionnally, H19 could act as an intra-group risk marker categorizing the biopsies in normal versus benign, versus precancerous breast tissue, and as a prognostic factor in cancerous lesions discriminating aggressive versus nonaggressive lesions. Our study suggests that the lncRNA H19 could be a potential marker for breast cancer diagnosis, prognosis and risk management. |
format | Online Article Text |
id | pubmed-7747713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77477132020-12-22 The long non coding RNA H19 as a biomarker for breast cancer diagnosis in Lebanese women Elias-Rizk, Tamina El Hajj, Joelle Segal-Bendirdjian, Evelyne Hilal, George Sci Rep Article Breast cancer is the most common cancer in women worldwide. Minimally invasive percutaneous image-guided biopsies are the current cornerstone in the diagnosis of breast lesions detected on mammography/ultrasonography/MRI or palpable clinically. However, apparently benign breast disease seen on benign biopsies is a limiting factor for diagnosis and a risk factor of breast cancer especially in the high-risk category patients. Hypothesizing that molecular changes often occur before morphological variations, the levels of the LncRNA H19 were measured in anonymous tissues obtained from 79 women’s image guided breast biopsies, and correlated with cancer progression and aggressiveness. Using a double-blinded approach, H19 might be attributed an interesting role of a more sensitive biomarker in core breast biopsies, independently of the radiological/clinical classification and distant from the clinical management. We established different thresholds for H19 levels in normal versus proliferative, versus malignant tissues. Additionnally, H19 could act as an intra-group risk marker categorizing the biopsies in normal versus benign, versus precancerous breast tissue, and as a prognostic factor in cancerous lesions discriminating aggressive versus nonaggressive lesions. Our study suggests that the lncRNA H19 could be a potential marker for breast cancer diagnosis, prognosis and risk management. Nature Publishing Group UK 2020-12-17 /pmc/articles/PMC7747713/ /pubmed/33335214 http://dx.doi.org/10.1038/s41598-020-79285-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Elias-Rizk, Tamina El Hajj, Joelle Segal-Bendirdjian, Evelyne Hilal, George The long non coding RNA H19 as a biomarker for breast cancer diagnosis in Lebanese women |
title | The long non coding RNA H19 as a biomarker for breast cancer diagnosis in Lebanese women |
title_full | The long non coding RNA H19 as a biomarker for breast cancer diagnosis in Lebanese women |
title_fullStr | The long non coding RNA H19 as a biomarker for breast cancer diagnosis in Lebanese women |
title_full_unstemmed | The long non coding RNA H19 as a biomarker for breast cancer diagnosis in Lebanese women |
title_short | The long non coding RNA H19 as a biomarker for breast cancer diagnosis in Lebanese women |
title_sort | long non coding rna h19 as a biomarker for breast cancer diagnosis in lebanese women |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747713/ https://www.ncbi.nlm.nih.gov/pubmed/33335214 http://dx.doi.org/10.1038/s41598-020-79285-z |
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