4.7 Article

Membrane transport proteins in human melanoma: associations with tumour aggressiveness and metastasis

Journal

BRITISH JOURNAL OF CANCER
Volume 102, Issue 7, Pages 1157-1162

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/sj.bjc.6605590

Keywords

malignant melanoma; multiple drug resistance; MDR1/P-gp; MRP-1; immunohistochemistry

Categories

Funding

  1. Ireland's Higher Educational Authority Programme for Research in Third Level Institutions (PRTLI)
  2. Ireland's Health Research Board
  3. Trinity College Dublin [2008/2009]
  4. Science Foundation Ireland [08/SRC/B1410]

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BACKGROUND: Malignant melanoma, generally described as incurable, is notoriously refractory to chemotherapy. The mechanisms contributing to this have not yet been defined and the contributions of drug efflux pumps, implicated in chemo-resistance of many other cancer types, have not been extensively investigated in melanoma. METHODS: In this study, expression of multi-drug resistant (MDR1/P-gp and MRP-1) proteins was examined, by immunohistochemistry, in archival specimens from 134 melanoma patients. This included 92 primary tumours and 42 metastases. RESULTS: On assessing all specimens, MRP-1 and MDR1/P-gp expression was found to be common, with the majority (81%) of melanomas expressing at least one of these efflux pumps. Although there is significant association between expression of these pumps (P = 0.007), MRP-1 was found to be the predominant (67% of cases) form detected. chi(2) analysis showed significant associations between expression of MRP-1 and/or MDR1/P-gp and the aggressive nature of this disease specifically increased Breslow's depth, Clark's level and spread to lymph nodes. This association with aggressiveness and spread is further supported by the observation that a significantly higher percentage of metastases, than primary tumours, express MRP-1 (91% vs 57%; P<0.0001) and MDR1/P-gp (74% vs 50%; P = 0.010). CONCLUSION: The predominant expression of these pumps and, in particular, MRP-1 suggests that they may be important contributors to the inherent aggressive and resistant nature of malignant melanoma. British Journal of Cancer (2010) 102, 1157-1162. doi:10.1038/sj.bjc.6605590 www.bjcancer.com Published online 16 March 2010 (C) 2010 Cancer Research UK

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