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Modulation of MDR1 and MRP3 Gene Expression in Lung Cancer Cells after Paclitaxel and Carboplatin Exposure

Authors :
Jose Prados
Beatriz González
Consolación Melguizo
Raúl Ortiz
Octavio Caba
Pablo J. Álvarez
Raquel Luque
Antonia Aránega
[Melguizo,C
Prados,J
Álvarez,PJ
Aranega,A] Institute of Biopathology and Regenerative Medicine (IBIMER), Department of Anatomy and Human Embryology, School of Medicine, University of Granada, Granada, Sapin. [Luque,R
Gonzalez,B] Service of Medical Oncology, Virgen de las Nieves Hospital, Granada, Spain. [Ortiz,R
Caba,O] Department of Health Science, University of Jaén, Jaén, Spain.
This study was supported by the Instituto de Salud Carlos III (FIS) through Project no. PI11/01862, the Ministry of Science and Innovation (Project nos. SAF2009-12295 and GREIB.PT-2010-15) and the Consejería de Salud de la Junta de Andalucía through Projec no. PI-0338.
Source :
International Journal of Molecular Sciences, Volume 13, Issue 12, Pages 16624-16635, International Journal of Molecular Sciences, Vol 13, Iss 12, Pp 16624-16635 (2012)
Publication Year :
2012
Publisher :
MDPI AG, 2012.

Abstract

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.

Subjects

Subjects :
Lung Neoplasms
Resistencia a Antineoplásicos
Drug resistance
Pharmacology
lcsh:Chemistry
paclitaxel
chemistry.chemical_compound
Carcinoma, Non-Small-Cell Lung
Antineoplastic Combined Chemotherapy Protocols
Phenomena and Processes::Physiological Phenomena::Pharmacological Phenomena::Drug Resistance::Drug Resistance, Neoplasm [Medical Subject Headings]
MDR
Medicine
Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Genes, MDR [Medical Subject Headings]
lcsh:QH301-705.5
Spectroscopy
Regulation of gene expression
General Medicine
Neoplasm Proteins
Computer Science Applications
Gene Expression Regulation, Neoplastic
Paclitaxel
Neoplasias Pulmonares
carboplatin
Multidrug Resistance-Associated Proteins
Genes MDR
Chemicals and Drugs::Organic Chemicals::Hydrocarbons::Hydrocarbons, Cyclic::Hydrocarbons, Alicyclic::Cycloparaffins::Cyclodecanes::Taxoids::Paclitaxel [Medical Subject Headings]
ATP Binding Cassette Transporter, Subfamily B
MRP
Diseases::Neoplasms::Neoplasms by Site::Thoracic Neoplasms::Respiratory Tract Neoplasms::Lung Neoplasms [Medical Subject Headings]
Article
Catalysis
resistance
Inorganic Chemistry
Cell Line, Tumor
Humans
Physical and Theoretical Chemistry
Lung cancer
neoplasms
Molecular Biology
Dose-Response Relationship, Drug
business.industry
Organic Chemistry
medicine.disease
Carboplatin
Multiple drug resistance
lung cancer
lcsh:Biology (General)
lcsh:QD1-999
chemistry
Drug Resistance, Neoplasm
Cell culture
business
Chemicals and Drugs::Organic Chemicals::Organometallic Compounds::Organoplatinum Compounds::Carboplatin [Medical Subject Headings]

Details

ISSN :
14220067
Volume :
13
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences
Accession number :
edsair.doi.dedup.....084567dd29241a906554709d0d473089
Full Text :
https://doi.org/10.3390/ijms131216624