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Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer

The goal of this study was to identify a novel target for antibody-drug conjugate (ADC) development in triple negative breast cancer (TNBC), which has limited treatment options, using gene expression datasets and in vitro siRNA/CRISPR and in vivo functional assays. We analyzed 4467 breast cancers an...

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Autores principales: Wali, Vikram B., Patwardhan, Gauri A., Pelekanou, Vasiliki, Karn, Thomas, Cao, Jian, Ocana, Alberto, Yan, Qin, Nelson, Bryce, Hatzis, Christos, Pusztai, Lajos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797726/
https://www.ncbi.nlm.nih.gov/pubmed/31624295
http://dx.doi.org/10.1038/s41598-019-51453-w
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author Wali, Vikram B.
Patwardhan, Gauri A.
Pelekanou, Vasiliki
Karn, Thomas
Cao, Jian
Ocana, Alberto
Yan, Qin
Nelson, Bryce
Hatzis, Christos
Pusztai, Lajos
author_facet Wali, Vikram B.
Patwardhan, Gauri A.
Pelekanou, Vasiliki
Karn, Thomas
Cao, Jian
Ocana, Alberto
Yan, Qin
Nelson, Bryce
Hatzis, Christos
Pusztai, Lajos
author_sort Wali, Vikram B.
collection PubMed
description The goal of this study was to identify a novel target for antibody-drug conjugate (ADC) development in triple negative breast cancer (TNBC), which has limited treatment options, using gene expression datasets and in vitro siRNA/CRISPR and in vivo functional assays. We analyzed 4467 breast cancers and identified GABRP as top expressed gene in TNBC with low expression in most normal tissues. GABRP protein was localized to cell membrane with broad range of receptors/cell (815–53,714) and expressed by nearly half of breast cancers tissues. GABRP gene knockdown inhibited TNBC cell growth and colony formation in vitro and growth of MDA-MB-468 xenografts in nude mice. Commercially available anti-GABRP antibody (5–100 μg/ml) or de novo generated Fabs (20 μg/ml) inhibited TNBC cell growth in vitro. The same antibody conjugated to mertansine (DM1) also showed significant anticancer activity at nanomolar concentrations. Our results indicate that GABRP is a potential novel therapeutic target for ADC development.
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spelling pubmed-67977262019-10-25 Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer Wali, Vikram B. Patwardhan, Gauri A. Pelekanou, Vasiliki Karn, Thomas Cao, Jian Ocana, Alberto Yan, Qin Nelson, Bryce Hatzis, Christos Pusztai, Lajos Sci Rep Article The goal of this study was to identify a novel target for antibody-drug conjugate (ADC) development in triple negative breast cancer (TNBC), which has limited treatment options, using gene expression datasets and in vitro siRNA/CRISPR and in vivo functional assays. We analyzed 4467 breast cancers and identified GABRP as top expressed gene in TNBC with low expression in most normal tissues. GABRP protein was localized to cell membrane with broad range of receptors/cell (815–53,714) and expressed by nearly half of breast cancers tissues. GABRP gene knockdown inhibited TNBC cell growth and colony formation in vitro and growth of MDA-MB-468 xenografts in nude mice. Commercially available anti-GABRP antibody (5–100 μg/ml) or de novo generated Fabs (20 μg/ml) inhibited TNBC cell growth in vitro. The same antibody conjugated to mertansine (DM1) also showed significant anticancer activity at nanomolar concentrations. Our results indicate that GABRP is a potential novel therapeutic target for ADC development. Nature Publishing Group UK 2019-10-17 /pmc/articles/PMC6797726/ /pubmed/31624295 http://dx.doi.org/10.1038/s41598-019-51453-w Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wali, Vikram B.
Patwardhan, Gauri A.
Pelekanou, Vasiliki
Karn, Thomas
Cao, Jian
Ocana, Alberto
Yan, Qin
Nelson, Bryce
Hatzis, Christos
Pusztai, Lajos
Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer
title Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer
title_full Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer
title_fullStr Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer
title_full_unstemmed Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer
title_short Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer
title_sort identification and validation of a novel biologics target in triple negative breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797726/
https://www.ncbi.nlm.nih.gov/pubmed/31624295
http://dx.doi.org/10.1038/s41598-019-51453-w
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