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1 August 2002, Volume 21, Number 33, Pages 5108-5116
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Original Paper
Human rgr: transforming activity and alteration in T-cell malignancies
Peter Leonardi1, Ezra Kassin1, Inmaculada Hernandez-Muñoz1,2, Roberto Diaz1, Giorgio Inghirami1 and Angel Pellicer1

1Department of Pathology, 550 First Ave., New York University Medical Center, New York, NY 10016, USA

2The Netherlands Cancer Institute, Amsterdam, The Netherlands

Correspondence to: A Pellicer, E-mail: pellia01@endeavor.med.nyu.edu

Abstract

We have previously identified the oncogene rgr (ralGDS related) in DNA derived from a rabbit squamous cell carcinoma. Here we describe the identification of the human orthologue of the rabbit rgr gene termed hrgr (human ralGDS related). Four alternatively spliced full-length hrgr transcripts were isolated from normal human testes and liver libraries. Truncation of hrgr confers transforming ability to its cDNA. Using a RT-PCR assay we have been able to detect the expression of an abnormally truncated transcript in several human T-cell lymphoma lines, and in fresh tissue samples of patients with T-cell malignancies. In the DHL cell line, an Anaplastic Large Cell Lymphoma (ALCL) line, a DNA rearrangement was detected within the hrgr gene region. We propose that these T-cell lymphomas, at least in part, owe their malignant phenotypes to genetic alterations of the hrgr gene. These findings also raise the possibility that mutations in the hrgr gene are involved in other malignancies.

Oncogene (2002) 21, 5108-5116. doi:10.1038/sj.onc.1205694

Keywords

oncogene; rgr; lymphomas; gene rearrangement; Jurkat

Received 5 February 2002; revised 15 May 2002; accepted 20 May 2002
1 August 2002, Volume 21, Number 33, Pages 5108-5116
Table of contents    Previous  Abstract  Next   Full text  PDF
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