Abstract | BACKGROUND: METHODS: By immunohistochemical analysis, we investigated VEGF-C or CC chemokine receptor 7 expression, together with the lymphatic and blood vessel network, in 36 patients with primary skin melanomas and metastases at the sentinel lymph node biopsy (SLN-positive), and 26 melanoma patients with negative SLN biopsy (SLN-negative). RESULTS: We found that VEGF-C expression in primary melanoma specimens was significantly associated with SLN-positive (p < 0.001), particularly in thin melanomas. An association between augmented peritumoral lymphatic vessel area and SLN-positive (p < 0.02) was also seen. Conversely, no association between either expression of the CC chemokine receptor 7 in the primary tumor, or intratumoral lymphatic vessel or peritumoral and intratumoral blood vessel area, and SLN-positive was found. CONCLUSIONS: Our results, taking into account the expression of either VEGF-C or related histopathological markers, indicated the possibility to use VEGF-C immunohistochemistry as a marker of metastatic progression, especially in thin cutaneous melanomas.
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Authors | Francesca Cianfarani, Simona Mastroeni, Teresa Odorisio, Francesca Passarelli, Caterina Cattani, Thomas J Mannooranparampil, Cristina Fortes, Cristina M Failla |
Journal | Journal of cutaneous pathology
(J Cutan Pathol)
Vol. 39
Issue 9
Pg. 826-34
(Sep 2012)
ISSN: 1600-0560 [Electronic] United States |
PMID | 22804631
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2012 John Wiley & Sons A/S. |
Chemical References |
- Biomarkers, Tumor
- CCR7 protein, human
- Receptors, CCR7
- Vascular Endothelial Growth Factor C
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Topics |
- Adult
- Aged
- Biomarkers, Tumor
(biosynthesis)
- Female
- Gene Expression Regulation, Neoplastic
- Humans
- Lymphatic Metastasis
- Male
- Melanoma
(metabolism, pathology)
- Middle Aged
- Receptors, CCR7
(biosynthesis)
- Retrospective Studies
- Sentinel Lymph Node Biopsy
- Skin Neoplasms
(metabolism, pathology)
- Vascular Endothelial Growth Factor C
(biosynthesis)
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