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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/14495
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dc.contributor.authorZhao, Yaodong-
dc.contributor.authorWu, Qiong-
dc.contributor.authorZhou, Bin-
dc.contributor.authorXue, Yajun-
dc.contributor.authorLou, Meiqing-
dc.date.accessioned2022-12-02T04:40:46Z-
dc.date.available2022-12-02T04:40:46Z-
dc.date.issued2019-11-09-
dc.identifier.citationZhao, Y., Wu, Q., Zhou, B., Xue, Y., & Lou, M. (2019). Cytotropic heterogeneous molecular lipids inhibit the growth of glioma cells by inducing apoptosis and autophagy. Pakistan Journal of Pharmaceutical Sciences, 32(6).en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/14495-
dc.description.abstractThe cytotropic heterogeneous molecular lipid (CHML) is a mixture of lipids isolated from natural products. CHML is an effective therapy for various kinds of cancers; however, the effect of CHML on glioma cells was seldom reported. Here, we aim to explore the cytotoxicity of CHML on glioma cells, and analyze the possible mechanisms. U251 glioma cells were cultured with CHML at different concentration, and the growth inhibition was measured by CCK-8 assay. Induced apoptosis were detected by flow cytometry, and the induced autophagies were observed by a transmission electron microscope. The key molecules involved in apoptosis and autophagy were detected by quantitative PCR and western-blot. CHML might inhibit the growth of U251 cells and promote apoptosis by up-regulating the expressions of Caspase-8 and Caspase-3; CHML also induced autophagy of U251 cells by promoting the expressions of MAP LC-3 and Beclin-1. CHML can inhibit proliferation of U251 cells by promoting cell apoptosis and inducing autophagy.en_US
dc.language.isoenen_US
dc.publisherKarachi: Faculty of Pharmacy & Pharmaceutical Sciences, Karachien_US
dc.subjectCHMLen_US
dc.subjectgliomaen_US
dc.subjectapoptosisen_US
dc.subjectautophagyen_US
dc.titleCytotropic heterogeneous molecular lipids inhibit the growth of glioma cells by inducing apoptosis and autophagyen_US
dc.typeArticleen_US
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