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Secondary metabolites of mulberry leaves exert anti-lung cancer activity through regulating the PD-L1/PD-1 signaling pathway 被引量:1
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作者 Guiqin Ye Xin Sun +3 位作者 Jiuzhou Li Yuanyuan Mai Ruilan Gao Jianbin Zhang 《Journal of Pharmaceutical Analysis》 SCIE CAS CSCD 2024年第6期914-925,共12页
Lung cancer ranks the top of malignancies that cause cancer-related deaths worldwide.The leaves of Morus alba L are traditional Chinese medicine widely applied in respiratory diseases.Our previous work has demonstrate... Lung cancer ranks the top of malignancies that cause cancer-related deaths worldwide.The leaves of Morus alba L are traditional Chinese medicine widely applied in respiratory diseases.Our previous work has demonstrated the anti-lung cancer effect of secondary metabolites of mulberry leaf,but their mechanism of action has still not fully elucidated.We synthesized Moracin N(MAN)-Probe conjugated with alkyne to label lung cancer cells and identified protein targets by chemical proteomic analysis.MAN and its probe exerted similar growth-inhibitory effect on human lung cancer cells.Chemical proteomic results showed that MAN targeted the programmed death ligand 1(PD-L1)checkpoint pathway and T cell receptor(TCR)signaling pathway,indicating its immune-regulatory function.Cell-free surface plasmon resonance(SPR)results showed the direct interaction of MAN with PD-L1 protein.Molecular docking analysis demonstrated that MAN bound to E158 residue of PD-L1 protein.MAN downregulated the expression levels of PD-L1 in a time-and dose-dependent manner and disrupted the PD-L1/programmed death 1(PD-1)binding,including other secondary metabolites of mulberry leaves Guangsangon E(GSE)and Chalcomoracin(CMR).Human peripheral blood mononuclear cells(PBMCs)co-cultured with MAN-treated A549 cells,resulting in the increase of CD8^(+)GZMB^(+)T cells and the decrease of CD8^(+)PD-1^(+)T cells.It suggested that MAN exerts anti-cancer effect through blocking the PD-L1/PD-1 signaling.In vivo,MAN combined with anti-PD-1 antibody significantly inhibited lung cancer development and metastasis,indicating their synergistic effect.Taken together,secondary metabolites of mulberry leaves target the PD-L1/PD-1 signaling,enhance T cell-mediated immunity and inhibit the tumorigenesis of lung cancer.Their modulatory effect on tumor microenvironment makes them able to enhance the therapeutic efficacy of immune checkpoint inhibitors in lung cancer. 展开更多
关键词 Moracin N Click chemistry PD-L1 T cell Lung cancer
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Phenolic constituents and anticancer properties of Morus alba(white mulberry) leaves 被引量:20
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作者 Eric Wei Chiang Chan Siu Kuin Wong +2 位作者 Joseph Tangah Tomomi Inoue Hung Tuck Chan 《Journal of Integrative Medicine》 SCIE CAS CSCD 2020年第3期189-195,共7页
Flavonoids are by far the most dominant class of phenolic compounds isolated from Morus alba leaves(MAL). Other classes of compounds are benzofurans, phenolic acids, alkaloids, coumarins, chalcones and stilbenes. Majo... Flavonoids are by far the most dominant class of phenolic compounds isolated from Morus alba leaves(MAL). Other classes of compounds are benzofurans, phenolic acids, alkaloids, coumarins, chalcones and stilbenes. Major flavonoids are kuwanons, moracinflavans, moragrols and morkotins. Other major compounds include moracins(benzofurans), caffeoylquinic acids(phenolic acids) and morachalcones(chalcones). Research on the anticancer properties of MAL entailed in vitro and in vivo cytotoxicity of extracts or isolated compounds. Flavonoids, benzofurans, chalcones and alkaloids are classes of compounds from MAL that have been found to be cytotoxic towards human cancer cell lines. Further studies on the phytochemistry and anticancer of MAL are suggested. Sources of information were Pub Med,Pub Med Central, Science Direct, Google, Google Scholar, J-Stage, Pub Chem and China National Knowledge Infrastructure. 展开更多
关键词 FLAVONOIDS BENZOFURANS CYTOTOXIC moracins Morachalcones Chalcomoracin
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Moracin M的简便合成及其生物活性
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作者 李敏欣 杜文绒 +3 位作者 高金春 李磊 李艳平 毛泽伟 《合成化学》 CAS 2021年第7期624-627,共4页
以4-甲氧基水杨醛和3,5-二甲氧基溴化苄为原料,经取代、缩合和水解等3步反应,以38%的总收率合成了Moracin M。分别采用DPPH自由基清除法、小鼠巨噬细胞RAW264.7模型初步测试了Moracin M的抗氧化活性和体外抗炎活性,结果表明该化合物对D... 以4-甲氧基水杨醛和3,5-二甲氧基溴化苄为原料,经取代、缩合和水解等3步反应,以38%的总收率合成了Moracin M。分别采用DPPH自由基清除法、小鼠巨噬细胞RAW264.7模型初步测试了Moracin M的抗氧化活性和体外抗炎活性,结果表明该化合物对DPPH自由基的清除能力很强(IC_(50)=0.0433 mg/mL),优于阳性对照药V C,且具有一定的抗炎活性。 展开更多
关键词 Moracin M 合成 抗氧化活性 抗炎活性 4-甲氧基水杨醛 3 5-二甲氧基溴化苄
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