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芍药总苷通过促进黑色素瘤细胞中α5-烟碱型乙酰胆碱受体的降解诱导线粒体功能障碍和细胞凋亡。

Total Glucosides of Paeony Induce Mitochondrial Dysfunction and Apoptosis by Promoting the Degradation of α5-nAChR in Melanoma Cells.

作者信息

Meng Xianguang, Cheng Ling, Jiao Jing, Xing Yuanxin, Zhang Li

机构信息

Department of Dermatology, Jinan Central Hospital, Shandong University, Jinan, 250013, China.

Department of Neurology Medicine, The Second Hospital of Shandong University, Jinan, 250033, China.

出版信息

Comb Chem High Throughput Screen. 2025;28(9):1543-1552. doi: 10.2174/0113862073271585231129172213.

Abstract

BACKGROUND

Malignant melanoma is the leading cause of skin cancer-related death, with high malignancy and rapid progression. Total glucosides of paeony (TGP) are extracted from the roots of Paeonia Lactiflora Pall and are widely used in the treatment of chronic hepatitis, rheumatoid arthritis, and adjuvant therapy of tumor chemotherapy.

METHODS

In the present research, M14 and A375 cells were treated with TGP. CCK8, transwell and western blotting were performed to analyze the effect of TGP on cell function.

RESULTS

TGP treatment impeded the proliferation and migration and activated the apoptosis pathway in melanoma cells. Importantly, TGP induced the degradation of α5-nAChR. Overexpression of α5-nAChR inhibited the anti-cancer effect of TGP. In addition, TGP treatment released cytochrome c from mitochondria into the cytoplasm, inducing mitochondrial dysfunction in melanoma cells. TGP also inhibited the phosphorylation of P38-MAPK, and P38-MAPK inhibitor reduced the promoting effect of α5-nAChR in cell proliferation and migration.

CONCLUSION

TGP inhibited cell viability and migration and induced mitochondrial dysfunction and apoptosis by promoting the degradation of α5-nAChR in melanoma cells. This research provided a potential therapeutic anti-cancer drug for treatment strategies of melanoma.

摘要

背景

恶性黑色素瘤是皮肤癌相关死亡的主要原因,具有高恶性和快速进展的特点。芍药总苷(TGP)从芍药根中提取,广泛用于治疗慢性肝炎、类风湿关节炎以及肿瘤化疗的辅助治疗。

方法

在本研究中,用TGP处理M14和A375细胞。进行CCK8、Transwell和蛋白质免疫印迹分析TGP对细胞功能的影响。

结果

TGP处理抑制了黑色素瘤细胞的增殖和迁移,并激活了凋亡途径。重要的是,TGP诱导了α5-烟碱型乙酰胆碱受体(α5-nAChR)的降解。α5-nAChR的过表达抑制了TGP的抗癌作用。此外,TGP处理使细胞色素c从线粒体释放到细胞质中,诱导黑色素瘤细胞的线粒体功能障碍。TGP还抑制了P38丝裂原活化蛋白激酶(P38-MAPK)的磷酸化,并且P38-MAPK抑制剂降低了α5-nAChR对细胞增殖和迁移的促进作用。

结论

TGP通过促进黑色素瘤细胞中α5-nAChR的降解来抑制细胞活力和迁移,并诱导线粒体功能障碍和凋亡。本研究为黑色素瘤的治疗策略提供了一种潜在的治疗性抗癌药物。

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