Park Deokbae, Lee Jung-Hee, Yoon Sang-Pil
Department of Histology, College of Medicine, Jeju National University, Jeju 63243, Korea.
Department of Cellular and Molecular Medicine, Chosun University School of Medicine, Gwangju 61452, Korea.
Korean J Physiol Pharmacol. 2022 Sep 1;26(5):377-387. doi: 10.4196/kjpp.2022.26.5.377.
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.
苯并咪唑驱虫剂最近被重新用于克服对传统疗法耐药的癌症。为了评估苯并咪唑对耐药细胞的抗癌作用,在5-氟尿嘧啶耐药的结肠癌细胞中研究了各种细胞死亡途径。检测了野生型和5-氟尿嘧啶耐药的SNU-C5结肠癌细胞的活力,随后进行了蛋白质免疫印迹分析。还进行了细胞死亡和细胞周期的流式细胞术检测,以分析苯并咪唑的抗癌作用。与阿苯达唑相比,芬苯达唑对5-氟尿嘧啶耐药的SNU-C5细胞表现出更高的敏感性,并用于后续实验。流式细胞术显示,芬苯达唑在两种细胞中均显著诱导细胞凋亡以及细胞周期阻滞于G2/M期。与野生型SNU-C5细胞相比,5-氟尿嘧啶耐药的SNU-C5细胞自噬减少,铁死亡增加且铁死亡增强的细胞凋亡增加,半胱天冬酶-8和p53的激活减少。这些结果表明,芬苯达唑可能是5-氟尿嘧啶耐药癌细胞的一种潜在替代治疗方法,并且在5-氟尿嘧啶耐药的SNU-C5细胞中,芬苯达唑的抗癌活性不需要p53。