Effects of Recombinant Circularly Permuted Tumor Necrosis Factor (TNF)-Related Apoptosis-Inducing Ligand (TRAIL) (Recombinant Mutant Human TRAIL) in Combination with 5-Fluorouracil in Human Colorectal Cancer Cell Lines HCT116 and SW480

被引:10
作者
Sun, Tongyou [1 ]
Zhu, Tienian [2 ,3 ]
Liang, Xiujun [4 ]
Yang, Shifang [5 ]
Zhao, Ruijing [2 ]
机构
[1] Hebei Med Univ, Dept Oncol, Shijiazhuang, Hebei, Peoples R China
[2] Hebei Med Univ, Key Lab Immune Mech & Intervent Serious Dis Hebei, Dept Immunol, Shijiazhuang, Hebei, Peoples R China
[3] Bethune Int Peace Hosp, Dept Med Oncol, Shijiazhuang, Hebei, Peoples R China
[4] Chengde Med Univ, Basic Med Inst, Chengde, Hebei, Peoples R China
[5] Beijing Sunbio Biotech Co Ltd, Beijing, Peoples R China
来源
MEDICAL SCIENCE MONITOR | 2018年 / 24卷
基金
中国国家自然科学基金;
关键词
Apoptosis; Colorectal Neoplasms; Fluorouracil; Receptors; Death Domain; TNF-Related Apoptosis-Inducing Ligand; MULTIPLE-MYELOMA; PLUS THALIDOMIDE; IN-VIVO; CHEMOTHERAPY; THERAPY; DEATH; MECHANISMS; RESISTANT; IDENTIFICATION; ACTIVATION;
D O I
10.12659/MSM.909390
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Circularly permuted tumor necrosis factor-related apoptosis-inducing ligand, a mutant form of tumor necrosis factor-related apoptosis-inducing ligand, is an effective antitumor cytokine. However, its antitumor effect in colorectal cancer is unclear. This study assessed the antitumor effect of circularly permuted tumor necrosis factor-related apoptosis-inducing ligand alone or with 5-fluorouracil in colorectal cancer cells in vitro and explored the underlying mechanisms. Material/Methods: We used the (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) assay to analyze cell proliferation inhibition. The apoptotic effects of circularly permuted tumor necrosis factor-related apoptosis-inducing ligand, 5-fluorouracil, or both in human colorectal cancer cells were evaluated using flow cytometry. Furthermore, the levels of apoptosis-related proteins were examined by Western blotting. Results: Compared to either agent alone, cotreatment with 5-fluorouracil and circularly permuted tumor necrosis factor-related apoptosis-inducing ligand showed obvious antitumor effects and induced significant apoptosis of colorectal cancer cells. 5-Fluorouracil enhanced circularly permuted tumor necrosis factor-related apoptosis-inducing ligand-induced apoptosis by increasing death receptor 4 and 5 levels in HCT116 cells, but only of death receptor 4 in SW480 cells. Moreover, 5-fluorouracil plus circularly permuted tumor necrosis factor-related apoptosis-inducing ligand increased apoptosis-related protein levels such as cleaved caspase-3, caspase-8, and poly-ADP-ribose polymerase and downregulated that of the survival protein B-cell lymphoma-extra-large. Pretreatment with the pan-caspase inhibitor, z-VAD-FMK, attenuated the caspase-dependent apoptosis induced by circularly permuted tumor necrosis factor-related apoptosis-inducing ligand alone or combined with 5-fluorouracil. Conclusions: Cotreatment with 5-fluorouracil and circularly permuted tumor necrosis factor-related apoptosis-inducing ligand showed enhanced antitumor effects on colorectal cancer cells.
引用
收藏
页码:2550 / 2561
页数:12
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