Genes and Development

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GENES & DEVELOPMENT 21:1989-1992, 2007
©2007 by Cold Spring Harbor Laboratory Press; ISSN 0890-9369/ $5.00
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PERSPECTIVE

Targeting oncogenic Ras

Ernesto Diaz-Flores and Kevin Shannon1

Department of Pediatrics, University of California, San Francisco, California 94143, USA

The first 100 words of the full text of this article appear below.

Reversing the consequences of oncogenic Ras is a fundamental problem in cancer therapeutics. Somatic RAS mutations are highly prevalent in many human cancers that respond poorly to current treatments, including carcinomas of the lung, pancreas, and colon; melanoma; and myeloid leukemia (for review, see Schubbert et al. 2007Go). At first glance, oncogenic Ras is an appealing target for rational drug discovery as the mutant protein is a membrane-associated signaling molecule that is expressed at robust levels in primary tumor cells. However, targeting oncogenic Ras is extremely challenging in practice due to the nature of the Ras cycle and the . . . [Full Text of this Article]


    Oncogenic Ras: meek or macho?
 

    Oncogenic Ras in context
 

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Related Article

Oncogenic Ras-induced secretion of IL6 is required for tumorigenesis
Brooke Ancrile, Kian-Huat Lim, and Christopher M. Counter
Genes & Dev. 2007 21: 1714-1719. [Abstract] [Full Text] [PDF]






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Copyright © 2007 by Cold Spring Harbor Laboratory Press.