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Migrastatics-Anti-metastatic and Anti-invasion Drugs: Promises and Challenges

A. Gandalovičová, D. Rosel, M. Fernandes, P. Veselý, P. Heneberg, V. Čermák, L. Petruželka, S. Kumar, V. Sanz-Moreno, J. Brábek,

. 2017 ; 3 (6) : 391-406.

Language English Country United States

Document type Journal Article, Review

Grant support
NV15-32432A MZ0 CEP Register

In solid cancers, invasion and metastasis account for more than 90% of mortality. However, in the current armory of anticancer therapies, a specific category of anti-invasion and antimetastatic drugs is missing. Here, we coin the term 'migrastatics' for drugs interfering with all modes of cancer cell invasion and metastasis, to distinguish this class from conventional cytostatic drugs, which are mainly directed against cell proliferation. We define actin polymerization and contractility as target mechanisms for migrastatics, and review candidate migrastatic drugs. Critical assessment of these antimetastatic agents is warranted, because they may define new options for the treatment of solid cancers.

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$a In solid cancers, invasion and metastasis account for more than 90% of mortality. However, in the current armory of anticancer therapies, a specific category of anti-invasion and antimetastatic drugs is missing. Here, we coin the term 'migrastatics' for drugs interfering with all modes of cancer cell invasion and metastasis, to distinguish this class from conventional cytostatic drugs, which are mainly directed against cell proliferation. We define actin polymerization and contractility as target mechanisms for migrastatics, and review candidate migrastatic drugs. Critical assessment of these antimetastatic agents is warranted, because they may define new options for the treatment of solid cancers.
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$a Rosel, Daniel $u Department of Cell Biology, Charles University, Viničná 7, Prague, Czech Republic; Biotechnology and Biomedicine Centre of the Academy of Sciences and Charles University (BIOCEV), Průmyslová 595, 25242, Vestec u Prahy, Czech Republic.
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$a Fernandes, Michael $u Medbase, Chapel Hill, NC, USA.
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$a Veselý, Pavel $u Central European Institute of Technology, Brno University of Technology, Brno, Czech Republic.
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$a Heneberg, Petr $u Charles University, Department of Internal Medicine, Third Faculty of Medicine, Prague, Czech Republic.
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$a Čermák, Vladimír $u Department of Cell Biology, Charles University, Viničná 7, Prague, Czech Republic; Biotechnology and Biomedicine Centre of the Academy of Sciences and Charles University (BIOCEV), Průmyslová 595, 25242, Vestec u Prahy, Czech Republic.
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$a Petruželka, Luboš $u Department of Oncology, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.
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$a Kumar, Sunil $u Ayurveda Molecular Modeling, Hyderabad, Telangana, India.
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$a Sanz-Moreno, Victoria $u Tumor Plasticity Laboratory, Randall Division of Cell and Molecular Biophysics, Guy's Campus, King's College London, London, UK. Electronic address: victoria.sanz_moreno@kcl.ac.uk.
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$a Brábek, Jan $u Department of Cell Biology, Charles University, Viničná 7, Prague, Czech Republic; Biotechnology and Biomedicine Centre of the Academy of Sciences and Charles University (BIOCEV), Průmyslová 595, 25242, Vestec u Prahy, Czech Republic. Electronic address: jan.brabek@natur.cuni.cz.
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