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大麻素 WIN 55,212-2 通过触发 ROS 介导的信号通路抑制人神经胶质瘤细胞生长。

Cannabinoid WIN 55,212-2 Inhibits Human Glioma Cell Growth by Triggering ROS-Mediated Signal Pathways.

机构信息

Postdoctoral Workstation, Taian City Central Hospital, Tai'an, Shandong 271000, China.

School of Medicine, Shandong University, Jinan, Shandong 270021, China.

出版信息

Biomed Res Int. 2021 Apr 22;2021:6612592. doi: 10.1155/2021/6612592. eCollection 2021.

Abstract

Glioblastoma is a highly invasive primary malignant tumor of the central nervous system. Cannabinoid analogue WIN 55,212-2 (WIN) exhibited a novel anticancer effect against human tumors. However, the anticancer potential and underlying mechanism of WIN against human glioma remain unclear. Herein, the anticancer efficiency and mechanism of WIN in U251 human glioma cells were investigated. The results showed that WIN dose-dependently inhibited U251 cell proliferation, migration, and invasion . WIN treatment also effectively suppressed U251 tumor spheroids growth . Further studies found that WIN induced significant apoptosis as convinced by the caspase-3 activation and release of cytochrome C. Mechanism investigation revealed that WIN triggered ROS-mediated DNA damage and caused dysfunction of VEGF-AKT/FAK signal axis. However, ROS inhibition effectively attenuated WIN-induced DNA damage and dysfunction of VEGF-AKT/FAK signal axis and eventually improved U251 cell proliferation, migration, and invasion. Taken together, our findings validated that WIN had the potential to inhibit U251 cell proliferation, migration, and invasion and induce apoptosis by triggering ROS-dependent DNA damage and dysfunction of VEGF-AKT/FAK signal axis.

摘要

胶质母细胞瘤是一种高度侵袭性的中枢神经系统原发性恶性肿瘤。大麻素类似物 WIN 55,212-2 (WIN) 对人类肿瘤表现出新颖的抗癌作用。然而,WIN 对人胶质瘤的抗癌潜力和潜在机制仍不清楚。在此,研究了 WIN 对 U251 人神经胶质瘤细胞的抗癌效率和机制。结果表明,WIN 呈剂量依赖性地抑制 U251 细胞增殖、迁移和侵袭。WIN 处理还能有效抑制 U251 肿瘤球的生长。进一步的研究发现,WIN 通过 caspase-3 激活和细胞色素 C 的释放诱导明显的细胞凋亡。机制研究表明,WIN 引发 ROS 介导的 DNA 损伤,并导致 VEGF-AKT/FAK 信号轴功能障碍。然而,ROS 抑制有效减弱了 WIN 诱导的 DNA 损伤和 VEGF-AKT/FAK 信号轴功能障碍,最终改善了 U251 细胞的增殖、迁移和侵袭。总之,我们的研究结果验证了 WIN 通过触发 ROS 依赖性 DNA 损伤和 VEGF-AKT/FAK 信号轴功能障碍,具有抑制 U251 细胞增殖、迁移和侵袭并诱导凋亡的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fd/8087470/aff34ad12741/BMRI2021-6612592.001.jpg

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