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Rho GTPases in Cancer Radiotherapy and Metastasis

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Specialty Oncology
Date 2020 Aug 11
PMID 32772212
Citations 8
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Abstract

Despite treatment advances, radioresistance and metastasis markedly impair the benefits of radiotherapy to patients with malignancies. Functioning as molecular switches, Rho guanosine triphosphatases (GTPases) have well-recognized roles in regulating various downstream signaling pathways in a wide range of cancers. In recent years, accumulating evidence indicates the involvement of Rho GTPases in cancer radiotherapeutic efficacy and metastasis, as well as radiation-induced metastasis. The functions of Rho GTPases in radiotherapeutic efficacy are divergent and context-dependent; thereby, a comprehensive integration of their roles and correlated mechanisms is urgently needed. This review integrates current evidence supporting the roles of Rho GTPases in mediating radiotherapeutic efficacy and the underlying mechanisms. In addition, their correlations with metastasis and radiation-induced metastasis are discussed. Under the prudent application of Rho GTPase inhibitors based on critical evaluations of biological contexts, targeting Rho GTPases can be a promising strategy in overcoming radioresistance and simultaneously reducing the metastatic potential of tumor cells.

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References
1.
Hodge R, Ridley A . Regulating Rho GTPases and their regulators. Nat Rev Mol Cell Biol. 2016; 17(8):496-510. DOI: 10.1038/nrm.2016.67. View

2.
Cardama G, Gonzalez N, Maggio J, Menna P, Gomez D . Rho GTPases as therapeutic targets in cancer (Review). Int J Oncol. 2017; 51(4):1025-1034. PMC: 5592879. DOI: 10.3892/ijo.2017.4093. View

3.
Ulu A, Frost J . Regulation of RhoA activation and cytoskeletal organization by acetylation. Small GTPases. 2016; 7(2):76-81. PMC: 4905257. DOI: 10.1080/21541248.2016.1171283. View

4.
Cherfils J, Zeghouf M . Regulation of small GTPases by GEFs, GAPs, and GDIs. Physiol Rev. 2013; 93(1):269-309. DOI: 10.1152/physrev.00003.2012. View

5.
Tang Z, Li C, Kang B, Gao G, Li C, Zhang Z . GEPIA: a web server for cancer and normal gene expression profiling and interactive analyses. Nucleic Acids Res. 2017; 45(W1):W98-W102. PMC: 5570223. DOI: 10.1093/nar/gkx247. View