Impact Factor 3.845 | CiteScore 3.92
More on impact ›

Original Research ARTICLE Provisionally accepted The full-text will be published soon. Notify me

Front. Pharmacol. | doi: 10.3389/fphar.2019.01124

Anti-tumour activity of Abnormal Cannabidiol and its analogue O-1602 in taxol-resistant preclinical models of breast cancer

Andrea Tomko1, Hilary Trask1, John C. Achenbach2,  Steven R. Hall1,  Kerry B. Goralski1,  Lee D. Ellis2 and  Denis J. Dupré1*
  • 1Dalhousie University, Canada
  • 2National Research Council Canada (NRC-CNRC), Canada

Cannabinoids exhibit anti-inflammatory and anti-tumorigenic properties. Contrary to most cannabinoids present in the Cannabis plant, some, such as O-1602 and abnormal cannabidiol, have no or only little affinity to the CB1 or CB2 cannabinoid receptors and instead exert their effects through other receptors. Here, we investigated whether the synthetic regioisomers of cannabidiol, abnormal cannabidiol, and a closely related compound, O-1602, display anti-tumorigenic effects in cellular models of breast cancer and whether it could reduce tumorigenesis in vivo. Several studies have shown the effects of cannabinoids on chemotherapy-sensitive breast cancer cell lines, but less is known about the anti-tumorigenic effects of cannabinoids in chemotherapy-resistant cell lines. Paclitaxel-resistant MDA-MB-231 and MCF-7 breast cancer cell lines were used to study the effect of O-1602 and abnormal cannabidiol on viability, apoptosis and migration. The effects of O-1602 and abnormal cannabidiol on cell viability could be completely blocked by the combination of GPR55 and GPR18-specific siRNAs. Both O-1602 and abnormal cannabidiol decreased viability in Paclitaxel-resistant breast cancer cells in a concentration-dependent manner through induction of apoptosis. The effect of these cannabinoids on tumor growth in vivo was studied in a zebrafish xenograft model. In this model, treatment with O-1602 and abnormal cannabidiol (2M) significantly reduced tumor growth. Our results suggest that atypical cannabinoids, like O-1602 and abnormal cannabidiol, exert anti-tumorigenic effects on Paclitaxel-resistant breast cancer cells. Due to their lack of central sedation and psychoactive effects, these atypical cannabinoids could represent new leads for the development of additional anti-cancer treatments when resistance to conventional chemotherapy occurs during the treatment of breast and possibly other cancers.

Keywords: cannabinoid, Taxol (paclitaxel), breast cancer, Apoptosis, cell migration, G protein coupled receptor (GPCR), Zebrafish, Xenograft animal model

Received: 17 Jun 2019; Accepted: 30 Aug 2019.

Copyright: © 2019 Tomko, Trask, Achenbach, Hall, Goralski, Ellis and Dupré. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Dr. Denis J. Dupré, Dalhousie University, Halifax, B3H 4R2, Nova Scotia, Canada, denis.dupre@dal.ca