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Cannabidiol, a Non-Psychoactive Cannabinoid Compound, Inhibits Proliferation and Invasion in U87-MG and T98G Glioma Cells through a Multitarget Effect
Author(s) -
Marta Solinas,
Paola Massi,
Valentina Cinquina,
Marta Valenti,
Daniele Bolognini,
Marzia Bruna Gariboldi,
Elena Monti,
Tiziana Rubino,
Daniela Parolaro
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0076918
Subject(s) - cannabidiol , glioma , pharmacology , mapk/erk pathway , cannabinoid , protein kinase b , angiogenesis , chemistry , cell growth , signal transduction , cancer research , biology , medicine , cannabis , biochemistry , receptor , psychiatry
In the present study, we found that CBD inhibited U87-MG and T98G cell proliferation and invasiveness in vitro and caused a decrease in the expression of a set of proteins specifically involved in growth, invasion and angiogenesis. In addition, CBD treatment caused a dose-related down-regulation of ERK and Akt prosurvival signaling pathways in U87-MG and T98G cells and decreased hypoxia inducible factor HIF-1α expression in U87-MG cells. Taken together, these results provide new insights into the antitumor action of CBD, showing that this cannabinoid affects multiple tumoral features and molecular pathways. As CBD is a non-psychoactive phytocannabinoid that appears to be devoid of side effects, our results support its exploitation as an effective anti-cancer drug in the management of gliomas.

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