{"title":"Trehalose Liposomes Inhibit the Growth of Glioblastoma Cell In vitro and In vivo","authors":"Keiji Kuwabara, H. Ichihara, Y. Matsumoto","doi":"10.35248/2157-2518.21.12.364","DOIUrl":null,"url":null,"abstract":"The inhibitory effects of trehalose liposomes (TL) composed of α-D-glycopyranosyl-α-D-glucopyranoside monomyristate and L-α-dimyristoylphosphatidylcholine on the growth of human glioblastoma (U-87MG) cells were evaluated. Induction of apoptosis was observed after fusion and accumulation of TL in U-87MG cell membranes. Increased membrane fluidity of U-87MG cells treated with TL was observed. TL caused apoptosis in U-87MG cells through the activation of mitochondria and apoptosis-inducing factor via a caspase-independent pathway. Tumor weights markedly decreased in orthotopic graft mouse models of glioblastoma (U-87MG) after intravenous administration of TL compared with those in the control group.","PeriodicalId":15209,"journal":{"name":"Journal of carcinogenesis & mutagenesis","volume":"161 1","pages":"1-5"},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of carcinogenesis & mutagenesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35248/2157-2518.21.12.364","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The inhibitory effects of trehalose liposomes (TL) composed of α-D-glycopyranosyl-α-D-glucopyranoside monomyristate and L-α-dimyristoylphosphatidylcholine on the growth of human glioblastoma (U-87MG) cells were evaluated. Induction of apoptosis was observed after fusion and accumulation of TL in U-87MG cell membranes. Increased membrane fluidity of U-87MG cells treated with TL was observed. TL caused apoptosis in U-87MG cells through the activation of mitochondria and apoptosis-inducing factor via a caspase-independent pathway. Tumor weights markedly decreased in orthotopic graft mouse models of glioblastoma (U-87MG) after intravenous administration of TL compared with those in the control group.