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[Cancer Research 64, 180-188, January 1, 2004]
© 2004 American Association for Cancer Research


Regular Articles

Parathyroid Hormone-Related Protein Is an Essential Growth Factor for Human Clear Cell Renal Carcinoma and a Target for the von Hippel-Lindau Tumor Suppressor Gene

Thierry Massfelder1, Herve Lang12, Eric Schordan1, Veronique Lindner13, Sylvie Rothhut1, Sandra Welsch1, Patricia Simon-Assmann4, Mariette Barthelmebs1, Didier Jacqmin2 and Jean-Jacques Helwig1

1Section of Renovascular Pharmacology and Physiology, Institut National de la Santé et de la Recherche Médicale-University Louis Pasteur, University Louis Pasteur School of Medicine, Strasbourg; Departments of 2Urology and 3Pathology, University Hospital, Strasbourg; and 4Institut National de la Santé et de la Recherche Médicale U381, Strasbourg-Hautepierre, France

Clear cell renal carcinoma (CCRC) is responsible for 2% of cancer-related deaths worldwide and is resistant to virtually all therapies, indicating the importance of a search for new therapeutic targets. Parathyroid hormone-related protein (PTHrP) is a polyprotein derived from normal and malignant cells that regulates cell growth. In the current study, we show that blocking PTHrP with antibodies or antagonizing the common parathyroid hormone (PTH)/PTHrP receptor, the PTH1 receptor, dramatically blunts the expansion of human CCRC in vitro by promoting cell death. Importantly, in nude mice, anti-PTHrP antibodies induced complete regression of 70% of the implanted tumors by inducing cell death. In addition, we demonstrate that the von Hippel-Lindau tumor suppressor protein, which functions as a gatekeeper for CCRC, negatively regulates PTHrP expression at the post-transcriptional level. These studies indicate that PTHrP is an essential growth factor for CCRC and is a novel target for the von Hippel-Lindau tumor suppressor protein. Taken together, these results strongly suggest that targeting the PTHrP/PTH1 receptor system may provide a new avenue for the treatment of this aggressive cancer in humans.




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Copyright © 2004 by the American Association for Cancer Research.