Julie Gardener
New Member
The CB1/CB2 receptor agonist WIN-55,212-2 reduces viability of human Kaposi's sarcoma cells in vitro
Tonia Luca 1,2, Giulia Di Benedetto 1, Mariagrazia Rita Scuderi 1, Marco Palumbo 3, Silvia Clementi 1, Renato Bernardini 1, and Giuseppina Cantarella 1 1 Department of Experimental and Clinical Pharmacology; University of Catania School of Medicine, 95125 Catania, Italy; 2 Fondazione Mediterranea "G.B. Morgagni", 95125, Catania, Italy; 3 Dept. of Microbiological and Gynecological Sciences, University of Catania School of Medicine, 95124 Catania, Italy. Corresponding Author:
Giuseppina Cantarella MD, PhD
Dipartimento di Farmacologia Sperimentale e Clinica Università di Catania -Città Universitaria
Viale Andrea Doria, 6
I-95125 Catania
Italy
Phone: +39 — 095 — 738.4085
Fax: +39 — 095 — 738.4229
gcantare@unict.it
S0014-2999(09)00515-9
DOI: doi: 10.1016/j.ejphar.2009.06.004
Reference: EJP 6596
Abstract
Kaposi's sarcoma is a highly vascularized mesenchymal neoplasm arising with multiple lesions of the skin. Endogenous cannabinoids have been shown to inhibit proliferation of a wide spectrum of tumor cells. We studied the effects of cannabinoids on human Kaposi's sarcoma cell proliferation in vitro. To do so, we first investigated the presence of the cannabinoid receptors CB1 and CB2 mRNAs in the human Kaposi's sarcoma cell line KS-IMM by RT-PCR and, subsequently, the effects of the mixed CB1/CB2 agonist WIN-55,212-2 (WIN) on cell proliferation in vitro. WIN showed antimitogenic effects on Kaposi's sarcoma cells. Western blot analysis of Kaposi's sarcoma lysates suggested that WIN treatment induced activation of both caspase-3 and -6, as well as increased phosphorylation of the stress kinase p38 and JNK, along with transient phopsphorylation of ERK1/2. To better characterize the involvement of each single CB receptor in cannabinoidinduced cell death, we incubated Kaposi's sarcoma cells with different selective cannabinoid receptor agonists, respectively ACEA (CB1) and JWH-133 (CB2). None of the agonists was able to induce KS-IMM cell apoptosis. Moreover, we co-incubated Kaposi's sarcoma cells with WIN-55,212-2 and either the CB1 receptor antagonist AM251, the CB2 receptor antagonist AM630, or a combination of both substances. The CB2 receptor antagonist AM630 was able to significantly increase survival of Kaposi's sarcoma cells treated with WIN. In view of the antiproliferative effects of cannabinoids on KS-IMM cells, one could envision the cannabinoid system as a potential target for pharmacological treatment of Kaposi's sarcoma.
Source: he CB1/CB2 receptor agonist WIN-55,212-2 reduces viability of human Kaposi's sarcoma cells in vitro
