Author
Listed:
- Helene R. McMurray
(Department of Biomedical Genetics,)
- Erik R. Sampson
(Department of Biomedical Genetics,)
- George Compitello
(Department of Biomedical Genetics,)
- Conan Kinsey
(Department of Biomedical Genetics,)
- Laurel Newman
(Department of Biomedical Genetics,)
- Bradley Smith
(Department of Biomedical Genetics,)
- Shaw-Ree Chen
(Department of Biomedical Genetics,)
- Lev Klebanov
(Department of Biostatistics and Computational Biology,
Charles University, Sokolovska 83, Praha-8, CZ-18675, Czech Republic)
- Peter Salzman
(Department of Biostatistics and Computational Biology,)
- Andrei Yakovlev
(Department of Biostatistics and Computational Biology,
James P. Wilmot Cancer Center, University of Rochester Medical Center, 601 Elmwood Avenue, Rochester, New York 14642, USA)
- Hartmut Land
(Department of Biomedical Genetics,
James P. Wilmot Cancer Center, University of Rochester Medical Center, 601 Elmwood Avenue, Rochester, New York 14642, USA)
Abstract
Cancer-inducing genes: Role of Ras/p53 synergy Oncogenes and/or the loss of tumour suppressor genes generally cooperate with each other in transforming cells into cancer cells. A new study identifies a list of genes synergistically regulated by the Ras oncogene and loss of the p53 tumour suppressor gene. Many of these genes are essential for tumour formation in vivo, whereas few of the genes regulated by either Ras or p53 alone are important. This establishes a new approach to finding genes important in tumorigenesis that may also represent novel targets for tumour therapy.
Suggested Citation
Helene R. McMurray & Erik R. Sampson & George Compitello & Conan Kinsey & Laurel Newman & Bradley Smith & Shaw-Ree Chen & Lev Klebanov & Peter Salzman & Andrei Yakovlev & Hartmut Land, 2008.
"Synergistic response to oncogenic mutations defines gene class critical to cancer phenotype,"
Nature, Nature, vol. 453(7198), pages 1112-1116, June.
Handle:
RePEc:nat:nature:v:453:y:2008:i:7198:d:10.1038_nature06973
DOI: 10.1038/nature06973
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