Anti-cancer effects of fenbendazole on 5-fluorouracil-resistant colorectal cancer cells

被引:8
|
作者
Park, Deokbae [1 ]
Lee, Jung-Hee [2 ]
Yoon, Sang-Pil [3 ]
机构
[1] Jeju Natl Univ, Coll Med, Dept Histol, Jeju 63243, South Korea
[2] Chosun Univ, Sch Med, Dept Cellular & Mol Med, Gwangju 61452, South Korea
[3] Jeju Natl Univ, Coll Med, Dept Anat, Jeju 63243, South Korea
来源
关键词
Apoptosis; Colorectal cancer; Drug resistance; Fenbendazole; p53; ANTHELMINTIC DRUG MEBENDAZOLE; COLON-CANCER; LUNG-CANCER; IN-VITRO; APOPTOSIS; PATHWAY; INACTIVATION; RESISTANCE; ARREST; LINES;
D O I
10.4196/kjpp.2022.26.5.377
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Benzimidazole anthelmintic agents have been recently repurposed to overcome cancers resistant to conventional therapies. To evaluate the anti-cancer effects of benzimidazole on resistant cells, various cell death pathways were investigated in 5-fluorouracil-resistant colorectal cancer cells. The viability of wild-type and 5-fluorouracil-resistant SNU-C5 colorectal cancer cells was assayed, followed by Western blotting. Flow cytometry assays for cell death and cell cycle was also performed to analyze the anti-cancer effects of benzimidazole. When compared with albendazole, fenbendazole showed higher susceptibility to 5-fluorouracil-resistant SNU-C5 cells and was used in subsequent experiments. Flow cytometry revealed that fenbendazole significantly induces apoptosis as well as cell cycle arrest at G2/M phase on both cells. When compared with wild-type SNU-C5 cells, 5-fluorouracil-resistant SNU-C5 cells showed reduced autophagy, increased ferroptosis and ferroptosis-augmented apoptosis, and less activation of caspase-8 and p53. These results suggest that fenbendazole may be a potential alternative treatment in 5-fluorouracil-resistant cancer cells, and the anticancer activity of fenbendazole does not require p53 in 5-fluorouracil-resistant SNU-C5 cells.
引用
收藏
页码:377 / 387
页数:11
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