Modulation of MDR1 and MRP3 Gene Expression in Lung Cancer Cells after Paclitaxel and Carboplatin Exposure
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Melguizo Alonso, Consolación; Prados Salazar, José Carlos; Camacho-Luque, Raquel; Ortiz Quesada, Raúl; Caba Pérez, Octavio; Álvarez, Pablo J.; Álvarez González, Beatriz; Aránega Jiménez, AntoniaEditorial
MDPI
Materia
Lung cancer Resistance MDR
Date
2012-12-05Referencia bibliográfica
Melguizo, C. et. al. Int. J. Mol. Sci. 2012, 13, 16624-16635. [https://doi.org/10.3390/ijms131216624]
Sponsorship
Instituto de Salud Carlos III (FIS) through Project no. PI11/01862; Ministry of Science and Innovation (Project nos. SAF2009-12295 and GREIB.PT-2010-15); Consejería de Salud de la Junta de Andalucía through Project no. PI-0338Abstract
Carboplatin-paclitaxel is a reference regimen in the treatment of locally advanced or disseminated non-small cell lung cancer (NSCLC). This paper discusses the multidrug resistance developed with this drug combination, which is one of the major obstacles to successful treatment. In order to understand and overcome the drug resistance pattern of NSCLC after carboplatin plus paclitaxel exposure, levels of mRNA expression of multidrug resistance 1 (MDR1) and multidrug resistance-associated protein 3 (MRP3) were investigated in primary NSCLC cell lines (A-549 and A-427) and a metastasis-derived NSCLC cell line (NODO). Our results showed that exposure of the three NSCLC lines to plasma concentrations of paclitaxel (5 μM) produced an increase in MDR1 expression, while MRP3 showed no alteration in expression. By contrast, the same cells exposed to carboplatin plasma concentrations (30 μM) showed overexpression of MRP3. In these cells, MDR1 showed no expression changes. Interestingly, the combination of both paclitaxel and carboplatin caused increased expression of the MDR1 drug resistance gene rather than the individual treatments. These results suggest that carboplatin and paclitaxel may induce drug resistance mediated by MDR1 and MRP3, which may be enhanced by the simultaneous use of both drugs.