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Carcinogenesis Advance Access originally published online on November 24, 2006
Carcinogenesis 2007 28(4):785-791; doi:10.1093/carcin/bgl210
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© The Author 2006. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Overexpression of iron regulatory protein 1 suppresses growth of tumor xenografts

Guohua Chen1,3, Carine Fillebeen1, Jian Wang1,4 and Kostas Pantopoulos1,2,*

1 Lady Davis Institute for Medical Research, Sir Mortimer B. Davis Jewish General Hospital 3755 Cote-Ste-Catherine Road, Montreal, Quebec, Canada H3T 1E2
2 Department of Medicine, McGill University Quebec, Canada
3 Present address: Division of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center TX, USA
4Present address: Department of Biochemistry, University of Texas Southwestern Medical Center TX, USA

*To whom correspondence should be addressed. Tel: +1 514 340 8260 ext. 5293; Fax: +1 514 340 7502; Email: kostas.pantopoulos{at}mcgill.ca

Iron is essential for proliferation of normal and neoplastic cells. Cellular iron uptake, utilization and storage are regulated by transcriptional and post-transcriptional mechanisms. We hypothesized that the disruption of iron homeostasis may modulate the growth properties of cancer cells. To address this, we employed H1299 lung cancer cells engineered for tetracycline-inducible overexpression of the post-transcriptional regulator iron regulatory protein 1 (IRP1). The induction of IRP1 (wild-type or the constitutive IRP1C437S mutant) did not affect the proliferation of the cells in culture, and only modestly reduced their efficiency to form colonies in soft agar. However, IRP1 dramatically impaired the capacity of the cells to form solid tumor xenografts in nude mice. Tumors derived from IRP1-transfectants were <20% in size compared to those from parent cells. IRP1 coordinately controls the expression of transferrin receptor 1 (TfR1) and ferritin by binding to iron-responsive elements (IREs) within their mRNAs. Biochemical analysis revealed high expression of epitope-tagged IRP1 in tumor tissue, which was associated with a profound increase in IRE-binding activity. As expected, this response misregulated iron metabolism by increasing TfR1 levels. Surprisingly, IRP1 failed to suppress ferritin expression and did not affect the levels of the iron transporter ferroportin. Our results show that the overexpression of IRP1 is associated with an apparent tumor suppressor phenotype and provide a direct regulatory link between the IRE/IRP system and cancer.

Abbreviations: IREs, iron-responsive elements; IRP1, iron regulatory protein 1; 2-ME, 2-mercaptoethanol; PBS, phosphate-buffered saline; TfR1, transferrin receptor 1

Received August 3, 2006; revised September 26, 2006; accepted October 21, 2006.


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