Abstract | BACKGROUND: Patients with metastazing malignant melanoma have a poor outcome and determination of thickness of the primary tumor remains as the most important prognostic predictor. The aim of this study was to use an antibody-based proteomics strategy to search for new molecular markers associated with melanoma progression. Two proteins, TRP-1 and galectin-1, were identified as proteins with enhanced expression in cells from the melanocytic lineage. PATIENTS AND METHODS:
Protein profiling of TRP-1 and galectin-1 together with proliferation marker Ki-67 and melanocyte marker Melan-A was performed in normal tissues from 144 individuals and in 216 different tumors using tissue microarrays and immunohistochemistry. The protein expression pattern was further analyzed in a defined cohort of 157 patients diagnosed with invasive cutaneous malignant melanoma. RESULTS: Both TRP-1 and galectin-1 were highly expressed in normal melanocytes and melanoma. The expression of TRP-1 was inversely correlated with tumor stage (p=0.002, (R=-0.28)). Neither TRP-1 or galectin-1 was associated with overall or disease free survival (p>0.14, p>0.46 respectively). Ki-67 was associated with tumor stage and survival (p<0.001). CONCLUSION:
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Authors | Asa Bolander, Margrét Agnarsdóttir, Sara Strömberg, Fredrik Ponten, Patrik Hesselius, Mathias Uhlen, Michael Bergqvist |
Journal | Cancer genomics & proteomics
(Cancer Genomics Proteomics)
2008 Nov-Dec
Vol. 5
Issue 6
Pg. 293-300
ISSN: 1109-6535 [Print] Greece |
PMID | 19287070
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Galectin 1
- Ki-67 Antigen
- LGALS1 protein, human
- Membrane Glycoproteins
- Neoplasm Proteins
- Oxidoreductases
- TYRP1 protein, human
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Topics |
- Disease-Free Survival
- Female
- Follow-Up Studies
- Galectin 1
(biosynthesis)
- Gene Expression Profiling
- Gene Expression Regulation, Neoplastic
- Humans
- Ki-67 Antigen
(biosynthesis)
- Male
- Melanocytes
- Melanoma
(metabolism, mortality)
- Membrane Glycoproteins
(biosynthesis, metabolism)
- Neoplasm Invasiveness
- Neoplasm Metastasis
- Neoplasm Proteins
(biosynthesis)
- Oxidoreductases
(biosynthesis, metabolism)
- Retrospective Studies
- Skin Neoplasms
(metabolism, mortality)
- Survival Rate
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