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Triple Negative Breast Cancer Profile, from Gene to microRNA, in Relation to Ethnicity
Breast cancer is the most frequent cause of cancer-related deaths among women worldwide. It is classified into four major molecular subtypes. Triple-negative breast cancers (TNBCs), a subgroup of breast cancer, are defined by the absence of estrogen and progesterone receptors and the lack of HER-2 e...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468678/ https://www.ncbi.nlm.nih.gov/pubmed/30871273 http://dx.doi.org/10.3390/cancers11030363 |
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author | Gupta, Ishita Sareyeldin, Rasha M. Al-Hashimi, Israa Al-Thawadi, Hamda A. Al Farsi, Halema Vranic, Semir Al Moustafa, Ala-Eddin |
author_facet | Gupta, Ishita Sareyeldin, Rasha M. Al-Hashimi, Israa Al-Thawadi, Hamda A. Al Farsi, Halema Vranic, Semir Al Moustafa, Ala-Eddin |
author_sort | Gupta, Ishita |
collection | PubMed |
description | Breast cancer is the most frequent cause of cancer-related deaths among women worldwide. It is classified into four major molecular subtypes. Triple-negative breast cancers (TNBCs), a subgroup of breast cancer, are defined by the absence of estrogen and progesterone receptors and the lack of HER-2 expression; this subgroup accounts for ~15% of all breast cancers and exhibits the most aggressive metastatic behavior. Currently, very limited targeted therapies exist for the treatment of patients with TNBCs. On the other hand, it is important to highlight that knowledge of the molecular biology of breast cancer has recently changed the decision-making process regarding the course of cancer therapies. Thus, a number of new techniques, such as gene profiling and sequencing, proteomics, and microRNA analysis have been used to explore human breast carcinogenesis and metastasis including TNBC, which consequently could lead to new therapies. Nevertheless, based on evidence thus far, genomics profiles (gene and miRNA) can differ from one geographic location to another as well as in different ethnic groups. This review provides a comprehensive and updated information on the genomics profile alterations associated with TNBC pathogenesis associated with different ethnic backgrounds. |
format | Online Article Text |
id | pubmed-6468678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64686782019-04-24 Triple Negative Breast Cancer Profile, from Gene to microRNA, in Relation to Ethnicity Gupta, Ishita Sareyeldin, Rasha M. Al-Hashimi, Israa Al-Thawadi, Hamda A. Al Farsi, Halema Vranic, Semir Al Moustafa, Ala-Eddin Cancers (Basel) Review Breast cancer is the most frequent cause of cancer-related deaths among women worldwide. It is classified into four major molecular subtypes. Triple-negative breast cancers (TNBCs), a subgroup of breast cancer, are defined by the absence of estrogen and progesterone receptors and the lack of HER-2 expression; this subgroup accounts for ~15% of all breast cancers and exhibits the most aggressive metastatic behavior. Currently, very limited targeted therapies exist for the treatment of patients with TNBCs. On the other hand, it is important to highlight that knowledge of the molecular biology of breast cancer has recently changed the decision-making process regarding the course of cancer therapies. Thus, a number of new techniques, such as gene profiling and sequencing, proteomics, and microRNA analysis have been used to explore human breast carcinogenesis and metastasis including TNBC, which consequently could lead to new therapies. Nevertheless, based on evidence thus far, genomics profiles (gene and miRNA) can differ from one geographic location to another as well as in different ethnic groups. This review provides a comprehensive and updated information on the genomics profile alterations associated with TNBC pathogenesis associated with different ethnic backgrounds. MDPI 2019-03-13 /pmc/articles/PMC6468678/ /pubmed/30871273 http://dx.doi.org/10.3390/cancers11030363 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Gupta, Ishita Sareyeldin, Rasha M. Al-Hashimi, Israa Al-Thawadi, Hamda A. Al Farsi, Halema Vranic, Semir Al Moustafa, Ala-Eddin Triple Negative Breast Cancer Profile, from Gene to microRNA, in Relation to Ethnicity |
title | Triple Negative Breast Cancer Profile, from Gene to microRNA, in Relation to Ethnicity |
title_full | Triple Negative Breast Cancer Profile, from Gene to microRNA, in Relation to Ethnicity |
title_fullStr | Triple Negative Breast Cancer Profile, from Gene to microRNA, in Relation to Ethnicity |
title_full_unstemmed | Triple Negative Breast Cancer Profile, from Gene to microRNA, in Relation to Ethnicity |
title_short | Triple Negative Breast Cancer Profile, from Gene to microRNA, in Relation to Ethnicity |
title_sort | triple negative breast cancer profile, from gene to microrna, in relation to ethnicity |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468678/ https://www.ncbi.nlm.nih.gov/pubmed/30871273 http://dx.doi.org/10.3390/cancers11030363 |
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