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作 者:Qin Tang Wan Li Xiangjin Zheng Liwen Ren Jinyi Liu Sha Li Jinhua Wang Guanhua Du
机构地区:[1]The State Key Laboratory of Bioactive Substance and Function of Natural Medicines,Beijing,China [2]Key Laboratory of Drug Target Research and Drug Screen,Institute of Materia Medica,Chinese Academy of Medical Science and Peking Union Medical College,100050 Beijing,China
出 处:《Signal Transduction and Targeted Therapy》2021年第1期83-94,共12页信号转导与靶向治疗(英文)
基 金:This work was supported by grants from the National Natural Science Foundation of China(81803584 for Qin Tang);China Postdoctoral Science Foundation(2018M640093 for Qin Tang);National Natural Science Foundation of China(81573454 for Jinhua Wang,81703536 for Wan Li);Beijing Natural Science Foundation(7172142);CAMS Innovation Fund for Medical Sciences(2016-I2M-3-007);Technology Major Projects for“Major New Drugs Innovation and Development”(2018ZX09711001-005-025 and 2018ZX09711001-012).
摘 要:Lung cancer is the fastest growth rate of morbidity and mortality in nearly a decade,and remains difficult to treat.Furthermore,the molecular mechanisms underlying its development are still unclear.In this study,bioinformatics analysis showed that MELK was highly expressed in lung cancer and negatively correlated to the survival of lung adenocarcinoma(LUAD).Immunohistochemistry analysis of LUAD patient tissues revealed there were a high level of MELK expression in LUAD.Knockdown of MELK expression inhibits the migration and invasion of LUAD cells,which may be mediated by Twist1,Slug,MMP7,and N-catenin.Overexpression of MELK promoted the growth of LUAD cells in medium,3D Matrigel,and nude mice.Inhibition of MELK by OTSSP167 arrested cycle of LUAD cells at G2/M phase via PLK1-CDC25C-CDK1 pathway,and triggered apoptosis-mediated pyroptosis.Together,these data indicate that MELK is critical for metastasis,mitotic progression,and programmed death of LUAD and may be a promising therapeutic target for LUAD.
关 键 词:METASTASIS PLK1 LUNG
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