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[Cancer Research 52, 348-356, January 15, 1992]
© 1992 American Association for Cancer Research

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Molecular and Cellular Characterization of Human Renal Cell Carcinoma Cell Lines

P. Anglard1, E. Trahan, S. Liu, F. Latif, M. J. Merino, M. I. Lerman, B. Zbar and W. M. Linehan2

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

Recent studies have suggested that a tumor suppressor gene located in the region 3p21–26 of chromosome 3 is essential to the genesis of sporadic renal cell carcinoma (RCC) and that other tumor suppressor genes located on other chromosomes may be involved with progression of this malignancy.

The cellular heterogeneity of solid tumors complicates their analysis. In order to analyze a homogeneous population of tumor cells and identify genetic changes associated with histology in renal cortical tumors, we have established and characterized 35 RCC lines derived from tumor tissue from 31 patients with renal cell carcinomas. The overall success rate in establishing these cell lines from fresh or frozen specimens was 75% (18 of 24) and 35% (17 of 48), respectively. These lines differed in their morphology, growth rates, and tumorigenicity in athymic nude mice. Molecular characterization utilizing DNA fingerprinting and restriction fragment length polymorphism deletion analysis was performed to detect somatic mutations and loss of heterozygosity on the short arm of chromosome 3. Analysis revealed loss of heterozygosity on chromosome 3p in 25 cell lines derived from 28 informative nonpapillary forms of RCC (89%). Deletion-mapping analysis showed the retention of the distal locus, D3S18, in one of the RCC cell lines, which further localized the position of the putative tumor suppressor gene to the region proximal to D3S18. Although deletions on chromosome 3 have been recently suggested to be specific to the clear cell-type phenotype, our results revealed no correlation between loss of heterozygosity and clear or granular cell types.

1 Present address: Laboratoire de génétique moléculaire des eucaryotes du CNRS, Unité 184 de biologie moléculaire et de génie génétique de l'INSERM, Institut de Chimie Biologique, Faculté de médecine, 11 rue Humann, 67085 Strasbourg Cédex, France.

2 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 7/30/91. Accepted 11/ 1/91.




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Copyright © 1992 by the American Association for Cancer Research.