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[Cancer Research 54, 3077-3081, June 15, 1994]
© 1994 American Association for Cancer Research

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Suppression of Tumorigenicity of Human Prostate Cancer Cells by Introduction of Human Chromosome del(12)(q13)1

Nathalie G. Bérubé, Marsha D. Speevak and Mario Chevrette2

Department of Biochemistry, Faculty of Medicine, University of Ottawa, Ontario K1H 8M5, Canada

The introduction of normal chromosomes into tumor cells by microcell fusion-mediated transfer is a powerful technique to identify putative tumor suppressor genes. We have used this approach to independently transfer human chromosomes 3 and 12 into a human prostate cancer cell line, DU 145. We showed that while the extra copy of chromosome 3 had no effect on the in vivo tumorigenicity of these cells, microcell hybrids containing an introduced portion of chromosome 12 (12pter-12q13) exhibited complete suppression of tumorigenicity in athymic nude mice. The presence of a dual selectable marker facilitated the selection for cells having segregated del(12)(q13). Loss of this fragment in three different clones led to reexpression of the malignant phenotype. These results demonstrate that one or more genes on human chromosome 12 function as tumor suppressors of prostate carcinogenesis.

1 This work was supported by a grant from the Cancer Research Society, Montréal, Québec, Canada. N. G. B. and M. D. S. are recipients of Ontario Graduate Scholarships.

2 To whom requests for reprints should be addressed, at Department of Biochemistry, University of Ottawa, 451 Smyth Road, Ottawa, Ontario K1H 8M5, Canada.

Received 2/ 4/94. Accepted 5/ 3/94.




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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 © 1994 by the American Association for Cancer Research.