Literature DB >> 23583638

Mitosis-targeting therapies: a troubleshooting guide.

Elena Doménech1, Marcos Malumbres.   

Abstract

Several mitotic kinases and kinesins are currently considered as cancer targets based on their critical role during the cell division cycle and their significant level of expression in human tumors. Yet, their use is limited by the lack of selectivity against tumor cells, the low percentage of mitotic cells in many human tumors, and dose-limiting side-effects. As a consequence, initial clinical trials have shown limited responses. Despite these drawbacks, inhibiting mitosis is a promising strategy that deserves further development. Future advances will benefit from more specific inhibitors with better pharmacodynamic properties, a clear physiological characterization and cell-type-specific requirements of old and new mitotic targets, and rational strategies based on synthetic lethal interactions to improve selectivity against tumor cells.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23583638     DOI: 10.1016/j.coph.2013.03.011

Source DB:  PubMed          Journal:  Curr Opin Pharmacol        ISSN: 1471-4892            Impact factor:   5.547


  17 in total

Review 1.  Prime movers: the mechanochemistry of mitotic kinesins.

Authors:  Robert A Cross; Andrew McAinsh
Journal:  Nat Rev Mol Cell Biol       Date:  2014-04       Impact factor: 94.444

Review 2.  Trial watch - inhibiting PARP enzymes for anticancer therapy.

Authors:  Antonella Sistigu; Gwenola Manic; Florine Obrist; Ilio Vitale
Journal:  Mol Cell Oncol       Date:  2015-06-10

3.  AMPK and PFKFB3 mediate glycolysis and survival in response to mitophagy during mitotic arrest.

Authors:  Elena Doménech; Carolina Maestre; Lorena Esteban-Martínez; David Partida; Rosa Pascual; Gonzalo Fernández-Miranda; Esther Seco; Ramón Campos-Olivas; Manuel Pérez; Diego Megias; Katherine Allen; Miguel López; Asish K Saha; Guillermo Velasco; Eduardo Rial; Raúl Méndez; Patricia Boya; María Salazar-Roa; Marcos Malumbres
Journal:  Nat Cell Biol       Date:  2015-08-31       Impact factor: 28.824

4.  Aurora B Overexpression Causes Aneuploidy and p21Cip1 Repression during Tumor Development.

Authors:  Alejandra González-Loyola; Gonzalo Fernández-Miranda; Marianna Trakala; David Partida; Kumiko Samejima; Hiromi Ogawa; Marta Cañamero; Alba de Martino; Ángel Martínez-Ramírez; Guillermo de Cárcer; Ignacio Pérez de Castro; William C Earnshaw; Marcos Malumbres
Journal:  Mol Cell Biol       Date:  2015-08-03       Impact factor: 4.272

5.  Effects of Anticancer Drugs on Chromosome Instability and New Clinical Implications for Tumor-Suppressing Therapies.

Authors:  Hee-Sheung Lee; Nicholas C O Lee; Natalay Kouprina; Jung-Hyun Kim; Alex Kagansky; Susan Bates; Jane B Trepel; Yves Pommier; Dan Sackett; Vladimir Larionov
Journal:  Cancer Res       Date:  2016-02-02       Impact factor: 12.701

6.  Systems and synthetic biology approaches to cell division.

Authors:  Alireza Mashaghi; Cees Dekker
Journal:  Syst Synth Biol       Date:  2014-01-30

7.  The Aurora-A inhibitor MLN8237 affects multiple mitotic processes and induces dose-dependent mitotic abnormalities and aneuploidy.

Authors:  Italia Anna Asteriti; Erica Di Cesare; Fabiola De Mattia; Volker Hilsenstein; Beate Neumann; Enrico Cundari; Patrizia Lavia; Giulia Guarguaglini
Journal:  Oncotarget       Date:  2014-08-15

Review 8.  Chloroquine and hydroxychloroquine for cancer therapy.

Authors:  Gwenola Manic; Florine Obrist; Guido Kroemer; Ilio Vitale; Lorenzo Galluzzi
Journal:  Mol Cell Oncol       Date:  2014-07-15

Review 9.  Cross-Talk between AURKA and Plk1 in Mitotic Entry and Spindle Assembly.

Authors:  Italia Anna Asteriti; Fabiola De Mattia; Giulia Guarguaglini
Journal:  Front Oncol       Date:  2015-12-23       Impact factor: 6.244

Review 10.  Targeting the Mitotic Catastrophe Signaling Pathway in Cancer.

Authors:  Margaret M Mc Gee
Journal:  Mediators Inflamm       Date:  2015-09-27       Impact factor: 4.711

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