Apoptin induces pyroptosis of colorectal cancer cells via the GSDME-dependent pathway

上睑下垂 基因敲除 细胞凋亡 程序性细胞死亡 细胞生物学 半胱氨酸蛋白酶 癌细胞 化学 癌症研究 生物 癌症 生物化学 遗传学
作者
Zirui Liu,Yiquan Li,Yilong Zhu,Nan Li,Wenjie Li,Chao Shang,Gaojie Song,Shanzhi Li,Jianan Cong,Tingyu Li,Zhiru Xiu,Jing Lu,Chenchen Ge,Yang Xia,Yaru Li,Lili Sun,Xiao Li,Ningyi Jin
出处
期刊:International Journal of Biological Sciences [Ivyspring International Publisher]
卷期号:18 (2): 717-730 被引量:63
标识
DOI:10.7150/ijbs.64350
摘要

Apoptin is a small molecular weight protein encoded by the VP3 gene of chicken anemia virus (CAV). It can induce apoptosis of tumor cells and play anti-tumorigenic functions. In this study, we identified a time-dependent inhibitory role of apoptin on the viability of HCT116 cells. We also demonstrated that apoptin induces pyroptosis through cleaved caspase 3, and with a concomitant cleavage of gasdermin E (GSDME) rather than GSDMD. GSDME knockdown switched the apoptin-induced cell death from pyroptosis to apoptosis in vitro. Furthermore, we demonstrated that the effect of apoptin on GSDME-dependent pyroptosis could be mitigated by caspase-3 and caspase-9 siRNA knockdown. Additionally, apoptin enhanced the intracellular reactive oxygen species (ROS), causing aggregation of the mitochondrial membrane protein Tom20. Moreover, bax and cytochrome c were released to the activating caspase-9, eventually triggering pyroptosis. Therefore, GSDME mediates the apoptin-induced pyroptosis through the mitochondrial apoptotic pathway. Finally, using nude mice xenografted with HCT116 cells, we found that apoptin induces pyroptosis and significantly inhibits tumor growth. Based on this mechanism, apoptin may provide a new strategy for colorectal cancer therapy.

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