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Multidrug resistance-associated proteins in glaucoma surgery

  • Clinical Investigation
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Graefe's Archive for Clinical and Experimental Ophthalmology Aims and scope Submit manuscript

Abstract 

Background: Multidrug resistance (MDR) describes the phenomenon of cross-resistance between different cytostatic agents which are structurally and functionally dissimilar. Two recently discovered proteins, lung resistance protein (LRP) and the multidrug resistance-related protein (MRP) have been implicated in the development of MDR. Since resistance to chemotherapeutic agents is a common problem in filtration surgery, especially in cases of complicated glaucoma, we decided to investigate the presence of MRP and LRP in surgically removed Tenon specimens from glaucoma patients. Methods: The presence of MRP and LRP in surgically removed Tenon tissue (n=15) was analyzed by immunohistochemistry. The expression by cultured Tenon fibroblasts was assessed by reverse-transcriptase polymerase chain reaction (RT-PCR) and fluorocytometry. Results: LRP expression was detected in 8 of 10 Tenon specimens. Positive staining for MRP was obtained in 5 of 10 specimens. Negative controls with non-immune mouse IgG did not display any specific staining. RT-PCR and fluorocytometry revealed constitutive expression of MRP and LRP, at the RNA and protein level respectively, that was unaltered by pretreatment of the cells with mitomycin C or 5-fluorouracil. Conclusion: Our results demonstrate, that besides P-glycoprotein, other components of the MDR-system are present in conjunctival fibroblasts. Future developments in the use of chemotherapeutic agents in association with of filtration surgery need to take account of the presence of these counteracting mechanisms.

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Received: 1 February 2000 Revised: 2 May 2000 Accepted: 5 June 2000

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Esser, J., Esser, P., Mietz, H. et al. Multidrug resistance-associated proteins in glaucoma surgery. Graefe's Arch Clin Exp Ophthalmol 238, 727–732 (2000). https://doi.org/10.1007/s004170000184

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  • DOI: https://doi.org/10.1007/s004170000184

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