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[Cancer Research 57, 5009-5012, November 15, 1997]
© 1997 American Association for Cancer Research

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Loss of Heterozygosity Studies and Deletion Mapping Identify Two Putative Chromosome 14q Tumor Suppressor Loci in Renal Oncocytomas1

Rüdiger F. Schwerdtle, Andreas Winterpacht, Stephan Störkel, Walburgis Brenner, Rudolf Hohenfellner, Bernhard Zabel, Christoph Huber and Hans-Jochen Decker2

Clinic of Hematology/Oncology/Pneumology [R. F. S., C. H., H-J. D.], Children's Hospital [A. W., B. Z.], and Department of Urology [W. B., R. H.], Johannes Gutenberg University, 55101 Mainz; and Institute of Pathology, University of Witten-Herdecke, 42283 Wuppertal [S. S.], Germany

Renal oncocytoma is considered to be a benign tumor that shares some phenotypic features with chromophobe renal cell carcinoma (RCC). Recently, we described high frequencies of allelic loss at 1p, 2p, 6p, 10p, 13q, 14q, 17p, and 21q, which correlate significantly with the chromophobe subtype of RCC. To investigate the genetic relationship between these two entities, we examined 12 oncocytomas for loss of heterozygosity (LOH) at these regions. In addition, we included markers for 3p, 5q, 7q, 11p, and 22q. The only chromosomal region showing similarly high frequencies of allelic loss for both subtypes was 14q. Therefore, a genetic relationship between renal oncocytoma and chromophobe RCC seems questionable. Eight of 12 oncocytomas (67%) showed LOH at 14q, a frequency that was significantly higher (P < 0.001, x2 test) than the frequencies of LOH in all other regions. To define regions potentially harboring novel tumor suppressor genes, we performed multifluorescence microsatellite analysis with 13 markers spanning 14q. Interstitial deletions at different regions of 14q were detected, with the highest frequencies at D14S258 (14q23–24.3) and D14S292 (14q32.1–32.2). 14q LOH might be associated with advanced-stage RCCs or other tumors, but it does not seem to indicate progression in oncocytomas. Its role in pathogenesis of renal oncocytomas remains to be clarified. Here, we provide evidence for two distinct tumor suppressor gene loci at 14q in renal oncocytoma, which will be useful for further fine-mapping studies of these critical regions.

1 This work was supported by the Deutsche Forschungsgemeinschaft (Grant De 356/3-2).

2 To whom requests for reprints should be addressed, at the Clinic of Hematology/Oncology/Pneumology, Third Division of Medicine, Johannes Gutenberg University, Langenbeckstrasse 1, 55101 Mainz, Germany.

Received 8/18/97. Accepted 10/ 2/97.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1997 by the American Association for Cancer Research.