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Cannabidiol Overcomes Oxaliplatin Resistance by Enhancing NOS3- and SOD2-Induced Autophagy in Human Colorectal Cancer Cells

Authors :
Soyeon Jeong
Bu Gyeom Kim
Dae Yeong Kim
Bo Ram Kim
Jung Lim Kim
Seong Hye Park
Yoo Jin Na
Min Jee Jo
Hye Kyeong Yun
Yoon A. Jeong
Hong Jun Kim
Sun Il Lee
Han Do Kim
Dae Hyun Kim
Sang Cheul Oh
Dae-Hee Lee
Source :
Cancers, Vol 11, Iss 6, p 781 (2019)
Publication Year :
2019
Publisher :
MDPI AG, 2019.

Abstract

Although oxaliplatin is an effective chemotherapeutic drug for colorectal cancer (CRC) treatment, patients often develop resistance to it. Therefore, a new strategy for CRC treatment is needed. The purpose of this study was to determine the effect of cannabidiol (CBD), one of the components of the cannabis plant, in overcoming oxaliplatin resistance in CRC cells. We established oxaliplatin-resistant cell lines, DLD-1 R and colo205 R, in CRC DLD-1 and colo205 cells. Autophagic cell death was induced when oxaliplatin-resistant cells were treated with both oxaliplatin and CBD. Additionally, phosphorylation of nitric oxide synthase 3 (NOS3) was increased in oxaliplatin-resistant cells compared to that in parent cells. Combined treatment with oxaliplatin and CBD reduced phospho-NOS3 levels and nitric oxide (NO) production and resulted in the production of reactive oxygen species (ROS) by reducing the levels of superoxide dismutase 2, an antioxidant present in the mitochondria, causing mitochondrial dysfunction. Taken together, these results suggest that elevated phosphorylation of NOS3 is essential for oxaliplatin resistance. The combination of oxaliplatin and CBD decreased NOS3 phosphorylation, which resulted in autophagy, by inducing the overproduction of ROS through mitochondrial dysfunction, thus overcoming oxaliplatin resistance.

Details

Language :
English
ISSN :
20726694
Volume :
11
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
edsdoj.604140ffb871430c8562ab2c3def5974
Document Type :
article
Full Text :
https://doi.org/10.3390/cancers11060781