YLT-11, a novel PLK4 inhibitor, inhibits human breast cancer growth via inducing maladjusted centriole duplication and mitotic defect.
第一作者:
Qian,Lei
第一单位:
Lab of Medicinal Chemistry, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy, 610041, Chengdu, China.
作者:
主题词
乙酰胺类(Acetamides);抗肿瘤药(Antineoplastic Agents);乳腺肿瘤(Breast Neoplasms);CDC2蛋白激酶(CDC2 Protein Kinase);细胞系, 肿瘤(Cell Line, Tumor);细胞增殖(Cell Proliferation);中心粒(Centrioles);周期素依赖激酶抑制剂p21(Cyclin-Dependent Kinase Inhibitor p21);药物评价, 临床前(Drug Evaluation, Preclinical);女(雌)性(Female);基因表达调控, 肿瘤(Gene Expression Regulation, Neoplastic);人类(Humans);吲唑类(Indazoles);有丝分裂(Mitosis);蛋白激酶抑制剂(Protein Kinase Inhibitors);嘧啶类(Pyrimidines);RNA, 小分子干扰(RNA, Small Interfering);信号传导(Signal Transduction);存活率分析(Survival Analysis);肿瘤负荷(Tumor Burden);异种移植模型抗肿瘤试验(Xenograft Model Antitumor Assays);cdc25磷酸酶类(cdc25 Phosphatases)
DOI
10.1038/s41419-018-1071-2
PMID
30337519
发布时间
2021-12-04
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