Literature DB >> 15013523

Rho GTPases: potential candidates for anticancer therapy.

Salvador Aznar1, Pilar Fernández-Valerón, Carolina Espina, Juan Carlos Lacal.   

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.

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Year:  2004        PMID: 15013523     DOI: 10.1016/j.canlet.2003.08.035

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  35 in total

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2.  Cell shrinkage as a signal to apoptosis in NIH 3T3 fibroblasts.

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3.  The mitochondrial inner membrane GTPase, optic atrophy 1 (Opa1), restores mitochondrial morphology and promotes neuronal survival following excitotoxicity.

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4.  A photoactivatable small-molecule inhibitor for light-controlled spatiotemporal regulation of Rho kinase in live embryos.

Authors:  Allison R Morckel; Hrvoje Lusic; Laila Farzana; Jeffrey A Yoder; Alexander Deiters; Nanette M Nascone-Yoder
Journal:  Development       Date:  2012-01       Impact factor: 6.868

5.  Synergistic induction of apoptosis by HMG-CoA reductase inhibitor and histone deacetylases inhibitor in HeLa cells.

Authors:  Yehua Gan; Jian Wang; Joseph Coselli; Xing Li Wang
Journal:  Biochem Biophys Res Commun       Date:  2007-11-09       Impact factor: 3.575

6.  Small molecules discovered in a pathway screen target the Rho pathway in cytokinesis.

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Journal:  Nat Chem Biol       Date:  2010-05-02       Impact factor: 15.040

7.  Rac and Rho GTPases in cancer cell motility control.

Authors:  Matteo Parri; Paola Chiarugi
Journal:  Cell Commun Signal       Date:  2010-09-07       Impact factor: 5.712

8.  Signaling through Rho GTPase pathway as viable drug target.

Authors:  Qun Lu; Frank M Longo; Huchen Zhou; Stephen M Massa; Yan-Hua Chen
Journal:  Curr Med Chem       Date:  2009       Impact factor: 4.530

9.  A critical role for Rac1 in tumor progression of human colorectal adenocarcinoma cells.

Authors:  Carolina Espina; María Virtudes Céspedes; Miguel Angel García-Cabezas; María Teresa Gómez del Pulgar; Alicia Boluda; Lourdes García Oroz; Salvador A Benitah; Paloma Cejas; Manuel Nistal; Ramón Mangues; Juan Carlos Lacal
Journal:  Am J Pathol       Date:  2007-12-28       Impact factor: 4.307

10.  Differential role of human choline kinase alpha and beta enzymes in lipid metabolism: implications in cancer onset and treatment.

Authors:  David Gallego-Ortega; Ana Ramirez de Molina; Maria Angeles Ramos; Fatima Valdes-Mora; Maria Gonzalez Barderas; Jacinto Sarmentero-Estrada; Juan Carlos Lacal
Journal:  PLoS One       Date:  2009-11-12       Impact factor: 3.240

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