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[Cancer Research 51, 1071-1077, February 15, 1991]
© 1991 American Association for Cancer Research

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Molecular Analysis of Genetic Changes in the Origin and Development of Renal Cell Carcinoma

P. Anglard, K. Tory, H. Brauch, G. H. Weiss, F. Latif, M. J. Merino, M. I. Lerman, B. Zbar and W. M. Linehan1

Urologic Oncology Section, Surgery Branch, Division of Cancer Treatment [P. A., G. H. W., W. M. L.] and Laboratory of Pathology [M. J. M.], National Cancer Institute, Bethesda, Maryland 20892; and the Laboratory of Immunobiology, National Cancer Institute-Frederick Cancer Research Facility [K. T., H. B., M. L., B. Z.], Division of Cancer Biology and Diagnosis, National Cancer Institute, Frederick, Maryland 21701

Renal cell carcinoma has been characterized by an abnormality on the short arm of chromosome 3 which suggests the presence of a tumor suppressor gene at this location. In order to more precisely define the location of the renal cell carcinoma gene and to differentiate molecular changes occurring in early stages of renal neoplasia versus those occurring later in malignant progression, DNA from normal and tumor tissue from 60 patients with various stages of renal cell carcinoma was analyzed for loss of alleles at different chromosomal loci. In tumor tissue from 51 of 58 evaluable patients (88%) there was loss of heterozygosity at one or more of 10 loci tested on chromosome 3 independently of tumor stage. Analysis of the genotypes identified the distal portion of 3p bounded by D3S2 and D3S22 (3p21-26) as the region of the disease gene. In tumor tissue from patients with advanced renal cell carcinoma, we found loss of heterozygosity on chromosome 11p in 5 of 21 (24%), on chromosome 13 in 3 of 9 (33%), and on chromosome 17 in 2 of 19 (11%). We found no loss of heterozygosity at the loci on chromosomes 11, 13, or 17 in tumor tissue from patients with localized renal cell carcinoma (N = 5). These data suggest the existence of a tumor suppressor gene on chromosome 3p which may be essential to the genesis of sporadic renal cell carcinoma and that other tumor suppressor genes are associated with progression of this malignancy.

1 To whom requests for reprints should be addressed, at Urologic Oncology Section, Surgery Branch, National Cancer Institute, Bldg. 10, Room 2B47, Bethesda, MD 20892.

Received 9/ 7/90. Accepted 11/19/90.




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Copyright © 1991 by the American Association for Cancer Research.