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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6797726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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