Triple negative breast cancer: Deciphering the biology and heterogeneity

Triple negative breast cancer (TNBC) is a subtype of breast cancer (BC) with a heterogeneous nature that stains negatively for estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor 2 (HER2) during immunohistochemistry. Approximately 15---20% of all cases of breast canc...

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Main Authors: Uscanga Perales, Grecia Iris, Santuario Facio, Sandra Karina, Ortiz López, Rocío
Format: Article
Language:English
Published: UANL. Facultad de Medicina 2016
Online Access:http://eprints.uanl.mx/11733/1/S1665579616300667_S300_en.pdf
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author Uscanga Perales, Grecia Iris
Santuario Facio, Sandra Karina
Ortiz López, Rocío
author_facet Uscanga Perales, Grecia Iris
Santuario Facio, Sandra Karina
Ortiz López, Rocío
author_sort Uscanga Perales, Grecia Iris
collection Repositorio Institucional
description Triple negative breast cancer (TNBC) is a subtype of breast cancer (BC) with a heterogeneous nature that stains negatively for estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor 2 (HER2) during immunohistochemistry. Approximately 15---20% of all cases of breast cancer are triple negative phenotypes. Compared to patients with hormone receptor-positive cancer, TNBC patients are typically younger (<50 years), African American, and have a high incidence of mutations in BRCA1/2 genes. To date, not a single targeted therapy has been approved for TNBC treatment, and cytotoxic chemotherapy remains as the standard systemic treatment, meaning that TNBC is an aggressive subtype of breast cancer with a poor prognosis. In this review, the literature search was done up to date on which gene expression profile of TNBC has been analyzed in order to identify the consensus on molecular mechanisms involved in carcinogenesis and/or the prognostic markers of the disease. In conclusion, these studies have reported that TNBC is composed of several clusters or genomic signatures as basal keratins. They have also reported on their proliferation, luminal/basal apocrine, regulatory interferon, immune cells/immunoglobulin related to stem cells, epithelial-mesenchymal, androgen receptor and angiogenesis. However, not all research groups have reported reproducible results. This confirms the heterogeneous nature of TNBC and the need for research on uniform selection criteria. However, these discoveries have led to the proposal of new treatments, such as the addition of platinum salts, new combinations of therapeutic agents, some targeted therapies such as PARP inhibitors, and PI3K and androgen antagonists. There is no doubt that a better understanding of the nature of TNBC will allow individualized and more effective therapies.
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spelling eprints-117332016-11-17T19:38:46Z http://eprints.uanl.mx/11733/ Triple negative breast cancer: Deciphering the biology and heterogeneity Uscanga Perales, Grecia Iris Santuario Facio, Sandra Karina Ortiz López, Rocío Triple negative breast cancer (TNBC) is a subtype of breast cancer (BC) with a heterogeneous nature that stains negatively for estrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor 2 (HER2) during immunohistochemistry. Approximately 15---20% of all cases of breast cancer are triple negative phenotypes. Compared to patients with hormone receptor-positive cancer, TNBC patients are typically younger (<50 years), African American, and have a high incidence of mutations in BRCA1/2 genes. To date, not a single targeted therapy has been approved for TNBC treatment, and cytotoxic chemotherapy remains as the standard systemic treatment, meaning that TNBC is an aggressive subtype of breast cancer with a poor prognosis. In this review, the literature search was done up to date on which gene expression profile of TNBC has been analyzed in order to identify the consensus on molecular mechanisms involved in carcinogenesis and/or the prognostic markers of the disease. In conclusion, these studies have reported that TNBC is composed of several clusters or genomic signatures as basal keratins. They have also reported on their proliferation, luminal/basal apocrine, regulatory interferon, immune cells/immunoglobulin related to stem cells, epithelial-mesenchymal, androgen receptor and angiogenesis. However, not all research groups have reported reproducible results. This confirms the heterogeneous nature of TNBC and the need for research on uniform selection criteria. However, these discoveries have led to the proposal of new treatments, such as the addition of platinum salts, new combinations of therapeutic agents, some targeted therapies such as PARP inhibitors, and PI3K and androgen antagonists. There is no doubt that a better understanding of the nature of TNBC will allow individualized and more effective therapies. UANL. Facultad de Medicina 2016 Article PeerReviewed text en cc_by_nc_nd http://eprints.uanl.mx/11733/1/S1665579616300667_S300_en.pdf http://eprints.uanl.mx/11733/1.haspreviewThumbnailVersion/S1665579616300667_S300_en.pdf Uscanga Perales, Grecia Iris y Santuario Facio, Sandra Karina y Ortiz López, Rocío (2016) Triple negative breast cancer: Deciphering the biology and heterogeneity. Medicina universitaria, 18 (71). pp. 105-114. ISSN 1665-5796
spellingShingle Uscanga Perales, Grecia Iris
Santuario Facio, Sandra Karina
Ortiz López, Rocío
Triple negative breast cancer: Deciphering the biology and heterogeneity
thumbnail https://rediab.uanl.mx/themes/sandal5/images/online.png
title Triple negative breast cancer: Deciphering the biology and heterogeneity
title_full Triple negative breast cancer: Deciphering the biology and heterogeneity
title_fullStr Triple negative breast cancer: Deciphering the biology and heterogeneity
title_full_unstemmed Triple negative breast cancer: Deciphering the biology and heterogeneity
title_short Triple negative breast cancer: Deciphering the biology and heterogeneity
title_sort triple negative breast cancer deciphering the biology and heterogeneity
url http://eprints.uanl.mx/11733/1/S1665579616300667_S300_en.pdf
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