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

细胞凋亡 黑色素瘤 癌症研究 程序性细胞死亡 活力测定 p38丝裂原活化蛋白激酶 癌细胞 癌症 化学 医学 MAPK/ERK通路 磷酸化 内科学 生物化学
作者
Xianguang Meng,Ling Cheng,Jing Jiao,Yuanxin Xing,Zhang Li
出处
期刊:Combinatorial Chemistry & High Throughput Screening [Bentham Science]
卷期号:27
标识
DOI:10.2174/0113862073271585231129172213
摘要

background: Malignant melanoma is the leading cause of skin cancer-related death with high malignancy and rapid progression. Total glucosides of paeony (TGP) is extracted from the roots of Paeonia Lactiflora Pall and 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. objective: N/A 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.

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