Diaz-Valdivia, Natalia I, Calderon, Claudia C, Diaz, Jorge E, Lobos-Gonzalez, Lorena, Sepulveda, Hugo, Ortiz, Rina J, Martinez, Samuel, Silva, Veronica, Maldonado, Horacio J 
ORCID: 0000-0002-7017-5215, Silva, Patricio et al (show 6 more authors)
(2017)
Anti-neoplastic drugs increase caveolin-1-dependent migration, invasion and metastasis of cancer cells.
ONCOTARGET, 8 (67).
pp. 111943-111965.
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Abstract
Expression of the scaffolding protein Caveolin-1 (CAV1) enhances migration and invasion of metastatic cancer cells. Yet, CAV1 also functions as a tumor suppressor in early stages of cancer, where expression is suppressed by epigenetic mechanisms. Thus, we sought to identify stimuli/mechanisms that revert epigenetic CAV1 silencing in cancer cells and evaluate how this affects their metastatic potential. We reasoned that restricted tissue availability of anti-neoplastic drugs during chemotherapy might expose cancer cells to sub-therapeutic concentrations, which activate signaling pathways and the expression of CAV1 to favor the acquisition of more aggressive traits. Here, we used <i>in vitro</i> [2D, invasion] and <i>in vivo</i> (metastasis) assays, as well as genetic and biochemical approaches to address this question. Colon and breast cancer cells were identified where CAV1 levels were low due to epigenetic suppression and could be reverted by treatment with the methyltransferase inhibitor 5'-azacytidine. Exposure of these cells to anti-neoplastic drugs for short periods of time (24-48 h) increased CAV1 expression through ROS production and MEK/ERK activation. In colon cancer cells, increased CAV1 expression enhanced migration and invasion <i>in vitro</i> via pathways requiring Src-family kinases, as well as Rac-1 activity. Finally, elevated CAV1 expression in colon cancer cells following exposure <i>in vitro</i> to sub-cytotoxic drug concentrations increased their metastatic potential <i>in vivo</i>. Therefore exposure of cancer cells to anti-neoplastic drugs at non-lethal drug concentrations induces signaling events and changes in transcription that favor CAV1-dependent migration, invasion and metastasis. Importantly, this may occur in the absence of selection for drug-resistance.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | caveolin-1, epigenetic silencing, chemotherapy, cell signaling, reactive oxygen species |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 13 May 2019 08:50 |
| Last Modified: | 19 Jan 2023 00:46 |
| DOI: | 10.18632/oncotarget.22955 |
| Related URLs: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3040993 |
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