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Open Access

Modulation of multidrug resistance proteins by statins in human neuroblastoma

BMC Pharmacology20088(Suppl 1):A24

https://doi.org/10.1186/1471-2210-8-S1-A24

Published: 5 November 2008

Chemoresistance is a major problem during cancer treatment. ATP-binding cassette (ABC) transporter efflux is mainly responsible for this chemotherapeutics resistance of the tumour cells. We have recently observed that in the presence of statins SH-SY5Y neuroblastoma cells show enhanced susceptibility to doxorubicin-induced apoptosis which cannot be explained by simple additivity. In order to monitor ABC transporter activity as a possible source of statin-mediated additivity in doxorubicin-induced apoptosis, calcein uptake and release were analysed in human SH-SY5Y neuroblastoma cells. Simvastatin inhibited calcein uptake and release to the same extent as the well-described 1st generation ABC transporter inhibitor verapamil. Using the fluorescence behaviour of doxorubicin the accumulation of the anthracycline in SH-SY5Y neuroblastoma cells was visualised by confocal microscopy. The cumulating fluorescence intensity showed significant acceleration and accumulation under atorvastatin treatment. P-glycoprotein (ABCB1) is a heavyly glycosylated transporter for cytotoxic compounds. The protein appears as a double band, representing a mature fully glycosylated protein (~180 kDa) and a partially deglycosylated immature protein (~140 kDa) [1]. Atorvastatin reduced the mature 180 kDa protein band, suggesting an impairment of glycosylation. Treatment of the cells with tunicamycin, an inhibitor of the endogenous protein glycosylation in the endopolasmic reticulum, leads to the detection of the complete deglycosylated immature protein (~110 kDa). This assumption is corroborated by additional N-glycosidase F (PNGase) treatment of the human SH-SY5Y cells. The functional relevance of the deglycosylation of P-glycoprotein has been confirmed by enhanced doxorubicin accumulation in PNGase F-treated SH-SY5Y cells. In order to circumvent limited biological significance of the degenerated SH-SY5Y cell line primary human neuroblastoma cells were investigated. Similary, in the presence of statins enhanced doxorubicin accumulation was detectable and thereby corroborated the above described principle of action. Taken together, simvastatin and atorvastatin reduce the glycosylation of P-glycoprotein. Hence, statins reduce the activity of P-glycoprotein, which leads to an enhanced intracellular accumulation of doxorubicin. This explains the potentiated apoptosis by co-application of simvastatin and doxorubicin.

Declarations

Acknowledgements

The work was supported by the Herzfeldersche Familienstiftung and the GENAU-Dragon Project.

Authors’ Affiliations

(1)
Department of Pharmacology, Center of Biomolecular Medicine and Pharmacology, Medical University of Vienna
(2)
St. Anna Children's Cancer Research Institute

References

  1. Wang Y, Loo TW, Bartlett MC, Clarke DM: Modulating the folding of P-glycoprotein and cystic fibrosis transmembrane conductance regulator truncation mutants with pharmacological chaperones. Mol Pharmacol. 2007, 71: 751-758. 10.1124/mol.106.029926.View ArticlePubMedGoogle Scholar

Copyright

© Sieczkowski et al; licensee BioMed Central Ltd. 2008

This article is published under license to BioMed Central Ltd.

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