Disulfiram with or without metformin inhibits oesophageal squamous cell carcinoma in vivo

被引:25
|
作者
Jivan, Rupal [1 ]
Peres, Jade [2 ]
Damelin, Leonard Howard [3 ,4 ]
Wadee, Reubina [5 ]
Veale, Robin Bruce [1 ]
Prince, Sharon [2 ]
Mavri-Damelin, Demetra [1 ]
机构
[1] Univ Witwatersrand, Sch Mol & Cell Biol, Private Bag X3, ZA-2050 Johannesburg, South Africa
[2] Univ Cape Town, Div Cell Biol, Dept Human Biol, Fac Hlth Sci, ZA-7925 Cape Town, South Africa
[3] Univ Witwatersrand, Sch Pathol, Fac Hlth Sci, 7 York Rd, ZA-2193 Parktown, South Africa
[4] Natl Inst Communicable Dis NHLS, Ctr HIV & STPs, Cell Biol Grp, Private Bag X4, ZA-2131 Johannesburg, South Africa
[5] Univ Witwatersrand, Sch Pathol, Div Anat Pathol, Fac Hlth Sci, 7 York Rd, ZA-2193 Parktown, South Africa
基金
新加坡国家研究基金会;
关键词
Disulfiram; Autophagy; Protein degradation; Metformin; Oesophageal squamous cell carcinoma; Drug repurposing; CANCER-CELLS; PROTEASOME INHIBITORS; MULTIDRUG-RESISTANCE; ANTIALCOHOLISM DRUG; APOPTOSIS INDUCERS; AUTOPHAGY; BINDING; PROTEIN; ANGIOGENESIS; DEGRADATION;
D O I
10.1016/j.canlet.2017.12.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oesophageal squamous cell carcinoma (OSCC) is highly prevalent in developing countries but there has been little recent progress into efficacious yet affordable treatment strategies. Drug repurposing is one attractive approach for cancer therapy. Disulfiram (DSF), used to treat alcoholism, inhibits cancer growth and we previously found that DSF perturbs protein degradation/turnover pathways in vitro. This was enhanced by combining DSF with the anti-diabetic drug metformin (Met). Here, we investigated DSF with/without Met, against OSCC in vivo. Nude mice injected subcutaneously with the human OSCC cell line WHCO1, were treated with 30 mg/kg or 50 mg/kg DSF three times per week and with/without Met, for 21 days. DSF and DSF/Met-treated animals had significantly smaller tumours compared to untreated, vehicle and positive control cisplatin-treated groups. This effect for DSF was independent of copper, with no significant accumulation of copper in tumours, together with maintained proteasome activity. However, increases in total ubiquitinated proteins, LC3B-II, LAMP1 and p62 in DSF and DSF/Met groups, indicate that autophagy is inhibited. These findings show that DSF and DSF/Met significantly impede OSCC tumour growth in vivo and offer prospective alternative chemotherapy approaches for OSCC. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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