The anticancer gene ORCTL3 targets stearoyl-CoA desaturase-1 for tumour-specific apoptosis

被引:12
作者
AbuAli, G. [1 ]
Chaisaklert, W. [1 ]
Stelloo, E. [1 ]
Pazarentzos, E. [1 ]
Hwang, M-S [1 ]
Qize, D. [1 ]
Harding, S. V. [2 ]
Al-Rubaish, A. [3 ]
Alzahrani, Aj [3 ]
Al-Ali, A. [3 ]
Sanders, T. A. B. [2 ]
Aboagye, E. O. [4 ]
Grimm, S. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Div Expt Med, London W12 0NN, England
[2] Kings Coll London, Diabet & Nutr Sci Div, London, England
[3] Univ Dammam, Coll Med, Prince Mohammed Ctr Res & Consultat Studies, Dammam, Saudi Arabia
[4] Univ London Imperial Coll Sci Technol & Med, Div Canc, London W12 0NN, England
基金
美国国家卫生研究院;
关键词
CANCER-CELL METABOLISM; PROTEIN; DEATH; MEMBRANE; OBESITY; IDENTIFICATION; TRANSFORMATION; PROLIFERATION; METASTASIS; ADHESION;
D O I
10.1038/onc.2014.93
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
ORCTL3 is a member of a group of genes, the so-called anticancer genes, that cause tumour-specific cell death. We show that this activity is triggered in isogenic renal cells upon their transformation independently of the cells' proliferation status. For its cell death effect ORCTL3 targets the enzyme stearoyl-CoA desaturase-1 (SCD1) in fatty acid metabolism. This is caused by transmembrane domains 3 and 4, which are more efficacious in vitro than a low molecular weight drug against SCD1, and critically depend on their expression level. SCD1 is found upregulated upon renal cell transformation indicating that its activity, while not impacting proliferation, represents a critical bottleneck for tumourigenesis. An adenovirus expressing ORCTL3 leads to growth inhibition of renal tumours in vivo and to substantial destruction of patients' kidney tumour cells ex vivo. Our results indicate fatty acid metabolism as a target for tumour-specific apoptosis in renal tumours and suggest ORCTL3 as a means to accomplish this.
引用
收藏
页码:1718 / 1728
页数:11
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