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


ABSTRACT: 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??g/ml) or de novo generated Fabs (20??g/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.

SUBMITTER: Wali VB 

PROVIDER: S-EPMC6797726 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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

Wali Vikram B VB   Patwardhan Gauri A GA   Pelekanou Vasiliki V   Karn Thomas T   Cao Jian J   Ocana Alberto A   Yan Qin Q   Nelson Bryce B   Hatzis Christos C   Pusztai Lajos L  

Scientific reports 20191017 1


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  ...[more]

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