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

被引:18
|
作者
Wali, Vikram B. [1 ]
Patwardhan, Gauri A. [1 ]
Pelekanou, Vasiliki [2 ]
Karn, Thomas [3 ]
Cao, Jian [2 ]
Ocana, Alberto [1 ]
Yan, Qin [2 ]
Nelson, Bryce [4 ]
Hatzis, Christos [1 ]
Pusztai, Lajos [1 ]
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Yale Canc Ctr,Sect Med Oncol, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06510 USA
[3] Goethe Univ Frankfurt, Dept Obstet & Gynecol, Frankfurt, Germany
[4] Yale Univ, Yale Canc Biol Inst, Dept Pharmacol, New Haven, CT USA
关键词
RECEPTOR SUBUNIT; EXPRESSION; CYCLOPHOSPHAMIDE; FLUOROURACIL; CHEMOTHERAPY; MULTICENTER; COMBINATION; DOXORUBICIN; PACLITAXEL; PREDICTOR;
D O I
10.1038/s41598-019-51453-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 mu g/ml) or de novo generated Fabs (20 mu 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.
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页数:10
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