β-catenin contributes to cordycepin-induced MGMT inhibition and reduction of temozolomide resistance in glioma cells by increasing intracellular reactive oxygen species

• Published in: Cancer letters 2018-10, Vol.435, p.66-79
• Main Authors: Bi, Yiming, Li, Han, Yi, Dazhuang, Bai, Yang, Zhong, Sheng, Liu, Qiaochu, Chen, Yong, Zhao, Gang
• Format: Article
• Language: English
• Subjects: Acetylcysteine; Alkylation; Apoptosis; Brain cancer; Brain tumors; Cancer therapies; Cell cycle; Cell growth; Cordycepin; Deoxyribonucleic acid; DNA; DNA methylation; DNA methyltransferase; Drug resistance; Flow cytometry; GBM; Gene expression; Glioblastoma; Glioma; Glioma cells; Glutathione; GSH; GSK-3β; Inhibition; Intracellular; Leukemia; Methylguanine; O6-methylguanine-DNA methyltransferase; Proteins; Reactive oxygen species; ROS; Software; Temozolomide; Wnt protein; β-Catenin
• ISSN: 0304-3835; 1872-7980
• DOI: 10.1016/j.canlet.2018.07.040

Glioblastoma multiforme (GBM) is one of the most aggressive human tumors, and it has a poor prognosis. Temozolomide (TMZ) is the primary alkylating agent used to treat GBM. Nevertheless, a number of GBM patients are resistant to TMZ. Therefore, there is an urgent need for more effective therapeutic options. Cordycepin (COR) is a natural chemical with anti-tumor effects, although its mechanism of action is poorly understood. Several lines of evidence suggest that O6-methylguanine DNA methyltransferase (MGMT) repairs damaged DNA and contributes to drug resistance to TMZ in gliomas. The Wnt/β-catenin pathway regulates MGMT gene expression. However, whether cordycepin inhibits MGMT expression by downregulating the β catenin pathway and augmenting chemosensitivity to TMZ in glioma cells remains unclear. In the present study, we found that cordycepin inhibited the viability of glioma cells and induced apoptosis, cell cycle arrest, overproduction of reactive oxygen species (ROS) and reduction of glutathione (GSH) in vitro. Moreover, cordycepin significantly reduced tumor volume and prolonged median survival of tumor-bearing rats in vivo. We also found that cordycepin inhibited MGMT expression and augmented chemosensitivity to TMZ in glioma cells in vitro and in vivo, accompanied by downregulation of p-GSK-3β and β-catenin. Moreover, overexpression of MGMT reversed the synergistic effect of cordycepin and TMZ. Pharmacological inhibition of GSK-3β with CHIR-99021 or overexpression of β-catenin reversed cordycepin-induced reduction of cell viability, downregulation of β-catenin and MGMT, increase of apoptosis and reduction of TMZ resistance. Furthermore, we found that β-catenin regulated cordycepin-induced overproduction of ROS by decreasing GSH. Inhibition of ROS production with N-acetyl-l-cysteine (NAC) not only rescued the reduction of cell viability but also eliminated β-catenin and MGMT inhibition, prevented glioma cells apoptosis and reversed the synergistic effect of cordycepin and TMZ. Taken together, we demonstrated that β-catenin contributed to cordycepin-induced MGMT inhibition and reduction of TMZ resistance in glioma cells via increasing intracellular ROS. These results indicate that cordycepin may be a novel agent to improve GBM treatment, especially in TMZ-resistant GBM with high MGMT expression. •Cordycepin inhibited the viability of glioma cells in vitro and in vivo.•Cordycepin reduced the expression of MGMT and augmented TMZ-mediated chemotherapy i