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Molecular regulation of angiogenesis and tumorigenesis by signal transduction pathways: evidence of predictable and reproducible patterns of synergy in diverse neoplasms
Author(s): Arbiser JL
Source: SEMINARS IN CANCER BIOLOGY    Volume: 14    Issue: 2    Pages: 81-91    Published: APR 2004  
Times Cited: 21     References: 144     
Abstract: A large number of oncogenes, tumor suppressor genes, and signal transduction pathways have been described. Currently, a framework that allows prediction Of tumor behavior based upon oncogenes, tumor Suppressors, and signal transduction pathways is lacking. In 1869, Mendeleev published a periodic table of elements which allowed prediction of properties of elements based upon atomic weights that allowed prediction of chemical and physical properties of elements yet to be discovered.

In this paper, I will discuss recurrent patterns of synergy found in the literature and our laboratory between tumor suppressor genes. oncogenes, and signaling pathways that allows one to predict the signaling pathway in a given minor based upon the inactivation of a tumor suppressor gene. These patterns can be found in multiple different human neoplasms. Conversely, one call predict the inactivation of a tumor suppressor based upon the activation Status of a signaling pathway. This knowledge call be used by a clinician or pathologist with access to immunohistochemistry to make predictions based upon simple technologies and determine the signaling pathways involved in a patient's tumor. These strategies may be useful in the design of prevention and treatment strategies for cancer. Published by Elsevier Ltd.

Document Type: Review
Language: English
Reprint Address: Arbiser, JL (reprint author), Emory Univ, Sch Med, Dept Dermatol, WMB 5309,1639 Pierce Dr, Atlanta, GA 30322 USA
Addresses:
1. Emory Univ, Sch Med, Dept Dermatol, Atlanta, GA 30322 USA
Publisher: ACADEMIC PRESS LTD ELSEVIER SCIENCE LTD, 24-28 OVAL RD, LONDON NW1 7DX, ENGLAND
Subject Category: Oncology
IDS Number: 802XI
ISSN: 1044-579X
DOI: 10.1016/j.semcancer.2003.09.013
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