Medical Studies that Prove Cannabis Can Cure Brain Cancer (4)
Abstract
Recently, cannabinoids (CBs) have been
shown to possess antitumor properties. Because the psychoactivity of
cannabinoid compounds
limits their medicinal usage, we undertook the
present study to evaluate the in vitro antiproliferative ability of
cannabidiol
(CBD), a nonpsychoactive cannabinoid compound, on
U87 and U373 human glioma cell lines. The addition of CBD to the culture
medium led to a dramatic drop of mitochondrial
oxidative metabolism [3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H tetrazolium bromide test] and viability in glioma cells, in a concentration-dependent manner that was already evident 24
h after CBD exposure, with an apparent IC50 of 25 μM. The antiproliferative effect of CBD was partially prevented by the CB2 receptor antagonist N-[(1S)-endo-1,3,3-trimethylbicyclo[2,2,1]heptan-2-yl]-5-(4-chloro-3-methylphenyl)-1-(4-methylbenzyl)-pyrazole-3-carboxamide
(SR144528;
SR2) and α-tocopherol. By contrast, the CB1
cannabinoid receptor antagonist N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboximide
hydrochloride (SR141716; SR1), capsazepine (vanilloid receptor
antagonist), the inhibitors of ceramide
generation, or pertussis toxin did not counteract
CBD effects. We also show, for the first time, that the
antiproliferative
effect of CBD was correlated to induction of
apoptosis, as determined by cytofluorimetric analysis and single-strand
DNA staining,
which was not reverted by cannabinoid antagonists.
Finally, CBD, administered s.c. to nude mice at the dose of 0.5
mg/mouse,
significantly inhibited the growth of
subcutaneously implanted U87 human glioma cells. In conclusion, the
nonpsychoactive
CBD was able to produce a significant antitumor
activity both in vitro and in vivo, thus suggesting a possible
application
of CBD as an antineoplastic agent.
Footnotes
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This work was supported by a grant from the Cannabinoid Research Institute, affiliated with GW Pharmaceuticals, Oxford, UK, and by a grant from the Italian Ministry for University and Scientific and Technological Research (FIRST 2001).
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ABBREVIATIONS: CB, cannabinoid; CBD, cannabidiol; THC, Δ9-tetrahydrocannabinol; VR, vanilloid receptor; AEA, N-arachidonoylethanolamide (anandamide); MTT, 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H tetrazolium bromide; PMA, phorbol 12-myristate 13-acetate; WIN 55,212-2,R-(+)-[2,3-dihydro-5-methyl-3-[(morpholinyl)methyl]pyrrolo[1,2,3-de]-1,4-benzoxazinyl]-(1-napthanlenyl) methanone mesylate; SR141716A (SR2), N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3 carboximide hydrochloride; SR144528 (SR1), N-[(1S)-endo-1,3,3-trimethylbicyclo[2,2,1]heptan-2-yl]-5-(4-chloro-3-methylphenyl)-1-(4-methylbenzyl)-pyrazole-3-carboxamide; PBS, phosphate-buffered saline; PI, propidium iodide; ssDNA, single-strand DNA; ELISA, enzyme-linked immunosorbent assay; CPZ, capsazepine; PTX, pertussis toxin.
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DOI: 10.1124/jpet.103.061002.
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- Received October 3, 2003.
- Accepted November 7, 2003.
- The American Society for Pharmacology and Experimental Therapeutics.
- Paola Massi,
- Angelo Vaccani,
- Stefania Ceruti,
- Arianna Colombo,
- Maria P. Abbracchio and
- Daniela Parolaro
+ Author Affiliations
- Address correspondence to:
Daniela Parolaro, Dept. of Structural and Functional Biology, Pharmacology Unit and Center of Neuroscience, University of Insubria, Via A. da Giussano 10, 21052 Busto Arsizio (Varese), Italy. E-mail: daniela.parolaro@uninsubria.it
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