Identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priority

Triple-negative breast cancer (TNBC) remains a significant clinical and scientific challenge. The classification of TNBC is based on the lack of expression of the human epidermal growth factor 2, the estrogen receptor, and the progesterone receptor. TNBC accounts for more than 20% of all breast canc...

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Main Author: Bhooma Venkatraman
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:Cancer Translational Medicine
Subjects:
Online Access:http://www.cancertm.com/article.asp?issn=2395-3977;year=2016;volume=2;issue=5;spage=137;epage=146;aulast=Venkatraman
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spelling doaj-241c6a84394c40f1b4a6cc40cdba42b12020-11-24T23:28:54ZengWolters Kluwer Medknow PublicationsCancer Translational Medicine2395-39772395-30122016-01-012513714610.4103/2395-3977.192931Identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priorityBhooma VenkatramanTriple-negative breast cancer (TNBC) remains a significant clinical and scientific challenge. The classification of TNBC is based on the lack of expression of the human epidermal growth factor 2, the estrogen receptor, and the progesterone receptor. TNBC accounts for more than 20% of all breast cancers (BCs), has a poorer prognosis compared to other BC subtypes, and has no targeted therapeutics. Primarily, this review focuses on the heterogeneity of BC and the importance of molecular subtyping for the accurate classification of TNBC. Further, it seeks to identify the molecular "omic" gaps in subtyping TNBC and the role of membrane protein biomarkers that could potentially advance clinical and translational research in BC.http://www.cancertm.com/article.asp?issn=2395-3977;year=2016;volume=2;issue=5;spage=137;epage=146;aulast=VenkatramanBiomarkers and membrane proteinsbreast cancermetastasistriple negative
collection DOAJ
language English
format Article
sources DOAJ
author Bhooma Venkatraman
spellingShingle Bhooma Venkatraman
Identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priority
Cancer Translational Medicine
Biomarkers and membrane proteins
breast cancer
metastasis
triple negative
author_facet Bhooma Venkatraman
author_sort Bhooma Venkatraman
title Identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priority
title_short Identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priority
title_full Identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priority
title_fullStr Identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priority
title_full_unstemmed Identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priority
title_sort identifying gaps and relative opportunities for discovering membrane proteomic biomarkers of triple-negative breast cancer as a translational priority
publisher Wolters Kluwer Medknow Publications
series Cancer Translational Medicine
issn 2395-3977
2395-3012
publishDate 2016-01-01
description Triple-negative breast cancer (TNBC) remains a significant clinical and scientific challenge. The classification of TNBC is based on the lack of expression of the human epidermal growth factor 2, the estrogen receptor, and the progesterone receptor. TNBC accounts for more than 20% of all breast cancers (BCs), has a poorer prognosis compared to other BC subtypes, and has no targeted therapeutics. Primarily, this review focuses on the heterogeneity of BC and the importance of molecular subtyping for the accurate classification of TNBC. Further, it seeks to identify the molecular "omic" gaps in subtyping TNBC and the role of membrane protein biomarkers that could potentially advance clinical and translational research in BC.
topic Biomarkers and membrane proteins
breast cancer
metastasis
triple negative
url http://www.cancertm.com/article.asp?issn=2395-3977;year=2016;volume=2;issue=5;spage=137;epage=146;aulast=Venkatraman
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