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

G. AbuAli, W. Chaisaklert, E. Stelloo, E. Pazarentzos, M. S. Hwang, D. Qize, S. V. Harding, A. Al-Rubaish, A. J. Alzahrani, A. Al-Ali, T. A B Sanders, E. O. Aboagye, S. Grimm

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)

Abstract

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.

Original languageEnglish
Article numberN/A
Pages (from-to)1718-1728
Number of pages11
JournalOncogene
Volume34
Issue number13
Early online date28 Apr 2014
DOIs
Publication statusPublished - 26 Mar 2015

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