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dc.date.accessioned 2012-04-04T11:46:52Z
dc.date.available 2012-04-04T03:00:00Z
dc.date.issued 2012 es
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/8442
dc.description.abstract Glioblastoma is one of the most malignant brain tumors. Current treatments for glioblastoma usually make poor responses, and novel treatment strategies are extremely imperative. Cytochalasin E was reported to inhibit angiogenesis and tumor growth in some studies, but its effects on gliomas are still unknown. In this study, we found cytochalasin E inhibits U87 human glioblastoma cell growth in a very low concentration range of 10-8 to 10-6 M in a time and concentration dependent manner, and the IC50 were 1.17 ± 0.32 × 10-7 M for 48 h treatment, 6.65 ± 1.12 × 10-8 M for 72 h and 3.78 ± 1.30 × 10-8 M for 96 h. We also found cytochalasin E induces cell-cycle G2/M phase arrest (72 h-treatment of 10-6 M cytochalasin E caused 56.2 ± 6.1 % cells arrest in G2/M phase) and cell apoptosis (96 h-treatment of 10-6 M cytochalasin E induced 24.1 ± 4.2 % cells apoptosis). Thus, cytochalasin E is proposed as a potential agent for glioblastoma chemotherapy. es
dc.format.extent 147-151 es
dc.language en es
dc.subject Actinas es
dc.subject Glioma es
dc.subject Citocalasinas es
dc.subject Apoptosis es
dc.title Cytochalasin E, a potential agent for anti-glioma therapy, efficiently induces U87 human glioblastoma cell death es
dc.type Articulo es
sedici.identifier.uri http://www.latamjpharm.org/resumenes/31/1/LAJOP_31_1_2_1.pdf es
sedici.creator.person Xing, Biao es
sedici.creator.person Zhang, Guofeng es
sedici.creator.person Li, Meng es
sedici.creator.person Hu, Weixing es
sedici.creator.person Gu, Peiyuan es
sedici.creator.person Wei, Dong es
sedici.creator.person Xu, Jing es
sedici.creator.person Ma, Banyou es
sedici.creator.person Gu, Bing es
sedici.creator.person Chen, Gong es
sedici.creator.person Li, Junyang es
sedici.subject.materias Farmacia es
sedici.description.fulltext false es
mods.originInfo.place Colegio de Farmacéuticos de la Provincia de Buenos Aires es
sedici.subtype Comunicacion es
sedici.description.peerReview peer-review es
sedici2003.identifier ARG-FARM-ART-0000001930 es
sedici.relation.journalTitle Latin American Journal of Pharmacy es
sedici.relation.journalVolumeAndIssue vol. 31, no. 1 es


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