## Abstract ABCG2 (BCRP) is a member of the ATP‐binding cassette (ABC) family of cell surface transport proteins. ABCG2 expression occurs in a variety of normal tissues, and is relatively limited to primitive stem cells. ABCG2 expression is associated with the side population (SP) phenotype of Hoec
Folate deprivation induces BCRP (ABCG2) expression and mitoxantrone resistance in Caco-2 cells
✍ Scribed by Clara Lemos; Ietje Kathmann; Elisa Giovannetti; Henk Dekker; George L. Scheffer; Conceição Calhau; Gerrit Jansen; Godefridus J. Peters
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- French
- Weight
- 878 KB
- Volume
- 123
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
Folates can induce the expression and activity of the breast‐cancer‐resistance‐protein (BCRP) and the multidrug‐resistance‐protein‐1 (MRP1). Our aim was to study the time‐dependent effect of folate deprivation/supplementation on (i) BCRP and MRP expression and (ii) on drug resistance mediated by these transporters. Therefore Caco‐2 colon cancer cells usually grown in standard RPMI‐medium containing supraphysiological folic acid (FA) concentrations (2.3 μM; high‐folate, HF) were gradually adapted to more physiological folate concentrations (1 nM leucovorin (LV) or 1 nM FA; low‐folate, LF), resulting in the sublines Caco‐2‐LF/LV and Caco‐2‐LF/FA. Caco‐2‐LF/LV and LF/FA cells exhibited a maximal increase of 5.2‐ and 9.6‐fold for BCRP‐mRNA and 3.9‐ and 5.7‐fold for BCRP protein expression, respectively, but no major changes on MRP expression. Overexpression of BCRP in the LF‐cells resulted in 3.6‐ to 6.3‐fold resistance to mitoxantrone (MR), which was completely reverted by the BCRP inhibitor Ko143. On the other hand, LF‐adapted cells were markedly more sensitive to methotrexate than the HF‐counterpart, both after 4‐hr (9,870‐ and 23,923‐fold for Caco‐2‐LF/LV and LF/FA, respectively) and 72‐hr (11‐ and 22‐fold for Caco‐2‐LF/LV and LF/FA, respectively) exposure. Immunofluorescent staining observed with a confocal‐laser‐scan‐microscope revealed that in Caco‐2 cells (both HF and LF), BCRP is mainly located in the cytoplasm. In conclusion, folate deprivation induces BCRP expression associated with MR resistance in Caco‐2 cells. The intracellular localization of BCRP in these cells suggests that this transporter is not primarily extruding its substrates out of the cell, but rather to an intracellular compartment where folates can be kept as storage. © 2008 Wiley‐Liss, Inc.
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