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Ranolazine inhibits NaV1.5-mediated breast cancer cell invasiveness and lung colonization.
- Source :
-
Molecular cancer [Mol Cancer] 2014 Dec 11; Vol. 13, pp. 264. Date of Electronic Publication: 2014 Dec 11. - Publication Year :
- 2014
-
Abstract
- Background: Na(V)1.5 voltage-gated sodium channels are abnormally expressed in breast tumours and their expression level is associated with metastatic occurrence and patients' death. In breast cancer cells, Na(V)1.5 activity promotes the proteolytic degradation of the extracellular matrix and enhances cell invasiveness.<br />Findings: In this study, we showed that the extinction of Na(V)1.5 expression in human breast cancer cells almost completely abrogated lung colonisation in immunodepressed mice (NMRI nude). Furthermore, we demonstrated that ranolazine (50 μM) inhibited Na(V)1.5 currents in breast cancer cells and reduced Na(V)1.5-related cancer cell invasiveness in vitro. In vivo, the injection of ranolazine (50 mg/kg/day) significantly reduced lung colonisation by Na(V)1.5-expressing human breast cancer cells.<br />Conclusions: Taken together, our results demonstrate the importance of Na(V)1.5 in the metastatic colonisation of organs by breast cancer cells and indicate that small molecules interfering with Na(V) activity, such as ranolazine, may represent powerful pharmacological tools to inhibit metastatic development and improve cancer treatments.
- Subjects :
- Animals
Breast Neoplasms metabolism
Cell Line, Tumor
Cell Movement drug effects
Female
Humans
Mice
Mice, Nude
Neoplasm Metastasis drug therapy
Neoplasm Metastasis pathology
Ranolazine
Acetanilides pharmacology
Breast Neoplasms drug therapy
Breast Neoplasms pathology
Lung pathology
NAV1.5 Voltage-Gated Sodium Channel metabolism
Neoplasm Invasiveness pathology
Piperazines pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1476-4598
- Volume :
- 13
- Database :
- MEDLINE
- Journal :
- Molecular cancer
- Publication Type :
- Academic Journal
- Accession number :
- 25496128
- Full Text :
- https://doi.org/10.1186/1476-4598-13-264