Identification and Validation of a Novel Biologics Target in Triple Negative Breast Cancer.
Vikram B WaliGauri A PatwardhanVasiliki PelekanouThomas KarnJian CaoAlberto OcanaQin YanBryce NelsonChristos HatzisLajos PusztaiPublished in: Scientific reports (2019)
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.
Keyphrases
- gene expression
- genome wide
- dna methylation
- copy number
- cancer therapy
- crispr cas
- poor prognosis
- single cell
- diffusion weighted
- genome wide identification
- high throughput
- cell therapy
- magnetic resonance imaging
- diffusion weighted imaging
- amino acid
- genome editing
- high fat diet induced
- type diabetes
- computed tomography
- photodynamic therapy
- protein protein
- stem cells
- small molecule
- weight loss
- drug delivery
- insulin resistance
- transcription factor
- signaling pathway
- hyaluronic acid
- cell cycle arrest
- clinical evaluation