BGB-283, a Novel RAF Kinase and EGFR Inhibitor, Displays Potent Antitumor Activity in BRAF-Mutated Colorectal Cancers.
第一作者:
Zhiyu,Tang
第一单位:
Department of In Vivo Pharmacology, BeiGene (Beijing) Co., Ltd., Beijing, P.R. China.
作者:
主题词
动物(Animals);抗肿瘤药(Antineoplastic Agents);苯咪唑类(Benzimidazoles);催化域(Catalytic Domain);细胞系, 肿瘤(Cell Line, Tumor);细胞增殖(Cell Proliferation);结直肠肿瘤(Colorectal Neoplasms);细胞外信号调节MAP激酶类(Extracellular Signal-Regulated MAP Kinases);女(雌)性(Female);人类(Humans);MAP激酶信号系统(MAP Kinase Signaling System);小鼠, 近交BALB C(Mice, Inbred BALB C);小鼠, 近交NOD(Mice, Inbred NOD);小鼠, 裸(Mice, Nude);小鼠, SCID(Mice, SCID);模型, 分子(Models, Molecular);萘啶类(Naphthyridines);磷酰化(Phosphorylation);蛋白质结合(Protein Binding);蛋白质加工, 转译后(Protein Processing, Post-Translational);原癌基因蛋白质B-raf(Proto-Oncogene Proteins B-raf);肿瘤负荷(Tumor Burden);异种移植模型抗肿瘤试验(Xenograft Model Antitumor Assays);raf激酶类(raf Kinases)
DOI
10.1158/1535-7163.MCT-15-0262
PMID
26208524
发布时间
2020-09-30
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Molecular cancer therapeutics
2187-97页
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