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Evidence for the involvement of ecto-5'-nucleotidase (CD73) in drug resistance
P Ujházy1, E S Berleth, J M Pietkiewicz
1Grace Cancer Drug Center, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Abstract:
Increased ecto-5'-nucleotidase (ecto-5'NT) protein expression in several multidrug-resistant (MDR) cell lines, documented previously by our group, suggests that this enzyme is involved in drug resistance. Here, Northern blot analysis of selected cell lines and their MDR variants positively correlated ecto-5'NT protein with its mRNA expression. An inhibitor of ecto-5'NT enzymatic activity, alpha,beta-methyleneadenosine 5'-diphosphate (AMP-CP), was used to determine if functionally active enzyme had a role in drug resistance. AMP-CP (0.3 mM) reversed the resistance of ecto-5'NT-positive MDR cells (MCF7/A6, L1210/A) to doxorubicin, whereas it did not affect the doxorubicin sensitivity of the ecto-5'NT-negative parental cell lines or that of 2 ecto-5'NT-negative MDR cell lines (HL60/VCR and A2780/DX5). Furthermore, AMP-CP increased rhodamine uptake and inhibited rhodamine efflux from ecto-5'NT-positive MDR cells without affecting ecto-5'NT-negative MDR cells. The presence of exogenous adenosine (0.5 microM) circumvented AMP-CP-induced inhibition of rhodamine efflux from EL4/ADM cells. AMP-CP inhibited the growth of the ecto-5'NT-positive L1210/A MDR cells but had no effect on the growth of the parental cell line. Determination of intracellular ATP levels indicated that MDR cells which had increased ecto-5'NT expression also had a lower intracellular ATP level than their parental cells. Our results suggest that, in certain MDR cell lines, ecto-5'NT serves as a required accessory molecule in resistance mediated by ATP-dependent mechanisms and that growth-sustaining nucleosides are provided by this salvage pathway.
Insights
Ecto-5'-nucleotidase (ecto-5'NT) is linked to multidrug resistance (MDR) in cancer cells. Inhibiting ecto-5'NT with AMP-CP reversed drug resistance and affected cellular nucleoside salvage pathways.
Area of Science:
- Biochemistry
- Molecular Biology
- Cancer Research
Background:
- Multidrug resistance (MDR) is a major challenge in cancer therapy.
- Increased ecto-5'-nucleotidase (ecto-5'NT) protein expression was previously observed in MDR cell lines.
Purpose of the Study:
- To investigate the role of ecto-5'NT enzymatic activity in MDR.
- To determine if ecto-5'NT contributes to drug resistance through ATP-dependent mechanisms.
Main Methods:
- Northern blot analysis to correlate ecto-5'NT mRNA and protein expression.
- Inhibition of ecto-5'NT activity using alpha,beta-methyleneadenosine 5'-diphosphate (AMP-CP).
- Assessment of drug sensitivity (doxorubicin), rhodamine uptake/efflux, and intracellular ATP levels.
Main Results:
- AMP-CP reversed doxorubicin resistance in ecto-5'NT-positive MDR cells.
- AMP-CP increased rhodamine uptake and inhibited efflux in ecto-5'NT-positive MDR cells.
- MDR cells with high ecto-5'NT expression showed lower intracellular ATP levels.
Conclusions:
- Ecto-5'-nucleotidase plays a role in MDR, potentially via ATP-dependent mechanisms.
- Inhibition of ecto-5'NT can overcome drug resistance in certain cancer cell lines.
- Ecto-5'NT may contribute to MDR by supplying nucleosides through salvage pathways.