IntrinsicMDR-1 gene and P-glycoprotein expression in human melanoma cell lines
| Autor: | Michael Micksche, E. M. Kokoschka, Robert Pirker, Leonilla Elbling, Michael Minai-Pour, Walter Berger, Monika Vetterlein |
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| Rok vydání: | 1994 |
| Předmět: |
Cancer Research
Pathology medicine.medical_specialty Molecular Sequence Data Radioimmunoassay Gene Expression Malignancy Polymerase Chain Reaction Immunoenzyme Techniques Gene expression Tumor Cells Cultured medicine Humans ATP Binding Cassette Transporter Subfamily B Member 1 RNA Messenger Cytotoxicity Melanoma P-glycoprotein Messenger RNA Base Sequence biology medicine.disease Drug Resistance Multiple Multiple drug resistance Oncology Cell culture biology.protein Cancer research |
| Zdroj: | International Journal of Cancer. 59:717-723 |
| ISSN: | 1097-0215 0020-7136 |
| DOI: | 10.1002/ijc.2910590522 |
| Popis: | Metastatic malignant melanoma is considered a chemotherapy-refractory malignancy. A few previous studies have delivered contradictory results regarding the presence and functionality of P-glycoprotein (P-gp), a transmembranous protein associated with the classical multidrug resistance (cMDR), in malignant melanoma. Therefore we have investigated this issue on 33 cell lines established from primary and metastatic lesions of human malignant melanoma, comparing different cMDR detection methods. Immunocytochemically 33% of the cell lines stained positive for P-gp. The data correlated with those of a P-gp-radioimmunometric (antibody-binding) assay. When RT-PCR was used for MDR-1 mRNA determination, 76% of the melanoma cell lines scored positive. Slot-blot analysis was seen to be less sensitive than RT-PCR. Results from the functional P-gp assays, using daunomycin (DM) as MDR-substrate, showed no influence of P-gp expression on drug accumulation and cytotoxicity. However, the cMDR-modifier verapamil (VP) significantly increased both parameters in those melanoma cells with the highest P-gp levels. We conclude that cMDR is apparently not the decisive but probably a complementary protective mechanism against toxic agents in malignant melanoma. |
| Databáze: | OpenAIRE |
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