Integrating Genetic Approaches into the Discovery of Anticancer Drugs

Author:

Hartwell Leland H.1,Szankasi Philippe1,Roberts Christopher J.1,Murray Andrew W.1,Friend Stephen H.1

Affiliation:

1. L. H. Hartwell, P. Szankasi, and S. H. Friend are at the Seattle Project, Molecular Pharmacology Department, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. C. J. Roberts is at Rosetta Inpharmatics, Incorporated, 12040 115th Street NE, Kirkland, WA 98034, USA. A. W. Murray is in the Department of Physiology, University of California at San Francisco, 513 Parnassus Avenue, San Francisco, CA 94142–0444, USA.

Abstract

The discovery of anticancer drugs is now driven by the numerous molecular alterations identified in tumor cells over the past decade. To exploit these alterations, it is necessary to understand how they define a molecular context that allows increased sensitivity to particular compounds. Traditional genetic approaches together with the new wealth of genomic information for both human and model organisms open up strategies by which drugs can be profiled for their ability to selectively kill cells in a molecular context that matches those found in tumors. Similarly, it may be possible to identify and validate new targets for drugs that would selectively kill tumor cells with a particular molecular context. This article outlines some of the ways that yeast genetics can be used to streamline anticancer drug discovery.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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