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PMID: 15018892 Published · ppublish English Journal Article Review

Molecular regulation of angiogenesis and tumorigenesis by signal transduction pathways: evidence of predictable and reproducible patterns of synergy in diverse neoplasms.

Seminars in cancer biology ·Vol. 14 ·No. 2 ·2004-04-00 ·Pages 81-91

Arbiser JL

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 tumor based upon the inactivation of a tumor suppressor gene. These patterns can be found in multiple different human neoplasms. Conversely, one can predict the inactivation of a tumor suppressor based upon the activation status of a signaling pathway. This knowledge can 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.

MeSH Terms
Apoptosis/genetics DNA Methylation DNA-Binding Proteins/metabolism Genes, Tumor Suppressor Genes, p16 Genes, p53 Humans Mitogen-Activated Protein Kinases/metabolism Mutation/genetics Neoplasms/blood supply,genetics,metabolism Neovascularization, Pathologic/genetics,metabolism Protein Serine-Threonine Kinases/metabolism Proto-Oncogenes Signal Transduction Transcription Factor AP-1/metabolism Transcription Factor AP-2 Transcription Factors/metabolism p38 Mitogen-Activated Protein Kinases
Chemicals
DNA-Binding Proteins Transcription Factor AP-1 Transcription Factor AP-2 Transcription Factors Protein Serine-Threonine Kinases Mitogen-Activated Protein Kinases p38 Mitogen-Activated Protein Kinases NF-kappa B kinase
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Arbiser Jack L
Department of Dermatology, Emory University School of Medicine, WMB 5309, 1639 Pierce Drive, Atlanta, GA 30322, USA. jarbise@emory.edu
Article Info
Journal
Seminars in cancer biology
Abbr.
Semin Cancer Biol
ISSN
1044-579X
Published
2004-04-00
Pages
81-91
Language
English
Region
England
NLM ID
9010218
Subset
IM
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