Title of article
Rho GTPases: potential candidates for anticancer therapy
Author/Authors
Aznar، نويسنده , , Salvador and Fernلndez-Valerَn، نويسنده , , Pilar and Espina، نويسنده , , Carolina and Lacal، نويسنده , , Juan Carlos، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
11
From page
181
To page
191
Abstract
Low molecular weight Rho GTPases are proteins that, in response to diverse stimuli, control key cellular processes such as cell proliferation, apoptosis, lipid metabolism, cytoarchitecture, adhesion, migration, cell polarity, and transcriptional regulation. The high incidence of overexpression of some members of the Rho family of GTPases in human tumors suggests that these proteins are important in the carcinogenic process, and therefore potential candidates for a therapeutic intervention. In recent years, the characterization of downstream effectors to Rho GTPases has increased our understanding of the general cellular effects that permit aberrant proliferation and motility of tumor cells. In addition, several transcription factors have been identified to play important roles at various levels of Rho-induced tumorigenesis. Accordingly, drugs that specifically alter Rho signaling display antineoplastic properties both at the level of tumor growth and tumor metastasis. In this review, a brief summary of the progress made in understanding the biological functions elicited by Rho GTPases that contribute to tumor biology will be made. In addition, a description of new drugs available targeted to specific elements of Rho signaling with antineoplastic or antimetastatic activity is included.
Keywords
anticancer drugs , apoptosis , Rho GTPases , Human carcinogenesis , Rho effectors , IQGAP , p21-activated kinase , Transcriptional regulation , rock , Wiskott–Aldrich syndrome protein family
Journal title
Cancer Letters
Serial Year
2004
Journal title
Cancer Letters
Record number
1806223
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