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Science 7 November 1997:
Vol. 278. no. 5340, pp. 1036 - 1039
DOI: 10.1126/science.278.5340.1036

News

CANCER RESEARCH:
From Bench Top to Bedside

Marcia Barinaga

More than 2 decades of research on oncogenes and tumor suppressors may finally pay off in a new generation of more specific, less toxic, cancer drugs. Some have already yielded promising results in cell culture studies and in animals, and are moving into tests in humans--and more are on the way. The targets of these drugs include cell surface receptors through which growth factors exert their effects and oncogene products that transmit growth-stimulatory signals inside cells. Still others aim to compensate for oncogene or tumor-suppressor gene mutations that impair cells' ability to initiate programmed cell death or apoptosis. Researchers hope these new therapies will kill cancer cells more effectively, with less harm to normal cells.

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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Neutrophils Contribute to the Biological Antitumor Activity of Rituximab in a Non-Hodgkin's Lymphoma Severe Combined Immunodeficiency Mouse Model.
F. J. Hernandez-Ilizaliturri, V. Jupudy, J. Ostberg, E. Oflazoglu, A. Huberman, E. Repasky, and M. S. Czuczman (2003)
Clin. Cancer Res. 9, 5866-5873
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Antibody targeting studies in a transgenic murine model of spontaneous colorectal tumors.
R. W. Wilkinson, E. L. Ross, R. Poulsom, M. Ilyas, J. Straub, D. Snary, W. F. Bodmer, and S. J. Mather (2001)
PNAS
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Farnesyltransferase Inhibitor Induces Rapid Growth Arrest and Blocks p70s6k Activation by Multiple Stimuli.
B. K. Law, P. Norgaard, and H. L. Moses (2000)
J. Biol. Chem. 275, 10796-10801
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A Mutant Form of Human Protein Farnesyltransferase Exhibits Increased Resistance to Farnesyltransferase Inhibitors.
K. Del Villar, J. Urano, L. Guo, and F. Tamanoi (1999)
J. Biol. Chem. 274, 27010-27017
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DNA Damage Increases Sensitivity to Vinca Alkaloids and Decreases Sensitivity to Taxanes through p53-dependent Repression of Microtubule-associated Protein 4.
C. C. Zhang, J.-M. Yang, J. Bash-Babula, E. White, M. Murphy, A. J. Levine, and W. N. Hait (1999)
Cancer Res. 59, 3663-3670
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Signaling Inhibitors in the Clinic: New Agents and New Challenges.
G. Hudes (1999)
J. Clin. Oncol. 17, 1093
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Farnesyltransferase inhibitors induce cytochrome c release and caspase 3 activation preferentially in transformed cells.
N. Suzuki, J. Urano, and F. Tamanoi (1998)
PNAS 95, 15356-15361
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Farnesyltransferase inhibitors induce dramatic morphological changes of KNRK cells that are blocked by microtubule interfering agents.
N. Suzuki, K. Del Villar, and F. Tamanoi (1998)
PNAS 95, 10499-10504
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Leflunomide Inhibits Pyrimidine de Novo Synthesis in Mitogen-stimulated T-lymphocytes from Healthy Humans.
K. Ruckemann, L. D. Fairbanks, E. A. Carrey, C. M. Hawrylowicz, D. F. Richards, B. Kirschbaum, and H. A. Simmonds (1998)
J. Biol. Chem. 273, 21682-21691
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Antibody targeting studies in a transgenic murine model of spontaneous colorectal tumors.
R. W. Wilkinson, E. L. Ross, R. Poulsom, M. Ilyas, J. Straub, D. Snary, W. F. Bodmer, and S. J. Mather (2001)
PNAS 98, 10256-10260
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Science. ISSN 0036-8075 (print), 1095-9203 (online)