© 2002 by Oxford University Press
Journal of the National Cancer Institute, Vol. 94, No. 13, 1031-1032,
July 3, 2002
© 2002 Oxford University Press
CORRESPONDENCE |
Re: Blocking Oncogenic Ras Signaling for Cancer Therapy
Affiliations of authors: S. Canevari, M. Figini, Unit of Molecular Therapies, Department of Experimental Oncology, Istituto Nazionale Tumori, Milan, Italy; S. Biocca, Department of Neuroscience, University of Rome "Tor Vergata," Italy.
Correspondence to: S. Canevari, Ph.D., Department of Experimental Oncology, Istituto Nazionale Tumori, 20133 Milan, Italy(e-mail: Canevari@istitutotumori.mi.it).
| The first 10% of the full text of this article appears below. |
We congratulate Adjei (1) on his excellent, comprehensive, and timely review on Ras signaling and the therapeutic implications of blocking this signaling. Perhaps space constraints and a major focus on pharmacologic aspects prevented any discussion of a promising alternative approach to perturbing Ras membrane localization, namely, the diversion of intracellular trafficking by an intracellular antibody (Fig.1
).
| |||||||||||
This article has been cited by other articles:
![]() |
S. Cogoi, M. Paramasivam, B. Spolaore, and L. E. Xodo Structural polymorphism within a regulatory element of the human KRAS promoter: formation of G4-DNA recognized by nuclear proteins Nucleic Acids Res., June 1, 2008; 36(11): 3765 - 3780. [Abstract] [Full Text] [PDF] |
||||
