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[Cancer Research 65, 9607-9610, November 1, 2005]
© 2005 American Association for Cancer Research


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Hopping around the Tumor Genome: Transposons for Cancer Gene Discovery

Lara S. Collier and David A. Largaespada

Department of Genetics, Cell Biology and Development, The Arnold and Mabel Beckman Center for Transposon Research, The Cancer Center, University of Minnesota-Twin Cities, Minneapolis, Minnesota

Requests for reprints: David A. Largaespada, Department of Genetics, Cell Biology and Development, University of Minnesota-Twin Cities, 6-160 Jackson Hall, 321 Church Street Southeast, Minneapolis, MN 55455. Phone: 612-626-4979; E-mail: larga002{at}umn.edu.

Retroviruses are powerful insertional somatic mutagens that have been used for many landmark discoveries of cancer genes in model organisms. However, their use as a cancer gene discovery tool has been limited to only a few tissues, mainly the hematopoietic system and mammary gland. Recently, the Sleeping Beauty (SB) transposon system was shown to be useful for random somatic cell mutagenesis in mice, allowing the induction or acceleration of tumor formation both in the hematopoietic system and in sarcomas. In these tumors, SB transposons repeatedly "tagged" specific genes, both known and new cancer genes. These results indicate that the SB system has great potential both for generating specific mouse models of human cancer and for cancer gene discovery in a wide variety of tissues.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
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Copyright © 2005 by the American Association for Cancer Research.