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ME20-S as a Potential Biomarker for the Evaluation of Uveal Melanoma

Bande Rodriguez, Manuel Francisco; Santiago Varela, Maria; Mera Yáñez, Purificación; Piulats, J. M.; Blanco Teijeiro, María Jose; Rodriguez-Alvarez, M. X.; Capeáns Tomé, María del Carmen; Piñeiro Ces, Antonio; Pardo, M.
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URI: http://hdl.handle.net/20.500.11940/2077
PMID: 26523384
DOI: 10.1167/iovs.15-17183
ISSN: 0146-0404
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Texto completo disponible por cortesía de Invest Ophthalmol Vis Sci . 2015 Nov;56(12):7007-11. doi: 10.1167/iovs.15-17183. (323.2Kb)
Fecha de publicación
2015
Título de revista
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
Tipo de contenido
Artigo
DeCS
Adulto | Adulto Joven | Anciano | Anciano de 80 o más Años | Antígeno gp100 del Melanoma | Biomarcadores de Tumor | Ensayo de Inmunoadsorción Enzimática | Estudios Retrospectivos | Estudios de Seguimiento | Femenino | Melanoma | Neoplasias de la Úvea | Persona de Mediana Edad | Progresión de la Enfermedad
MeSH
Adult | Aged | Aged, 80 and over | Biomarkers, Tumor | Disease Progression | Enzyme-Linked Immunosorbent Assay | Female | Follow-Up Studies | Humans | Male | Melanoma | Middle Aged | Retrospective Studies | Uveal Neoplasms | Young Adult | gp100 Melanoma Antigen
Resumen
PURPOSE: We previously identified the presence of the melanocyte-specific secreted (ME20-S) glycoprotein in secretomes of uveal melanoma (UM) cultures. The aim of this study was to test for the presence and levels of ME20-S in the serum of patients with choroidal nevi and UM and correlate these levels with individual clinical data. METHODS: Serum ME20-S levels were determined by ELISA in 111 patients distributed into four categories (53 choroidal nevi, 30 untreated UM, 11 10-year disease-free [DF] UM, 17 hepatic metastatic UM) and 32 age- and sex-matched controls. ME20-S levels were correlated with individual clinical data. RESULTS: The UM and the metastatic groups showed significantly higher levels of serum ME20-S than the other groups (P < 0.001). ME20-S levels in the DF patients did not differ from those in the control group. In addition, log-transformed serum ME20-S levels showed a positive correlation with the thickness of the lesion mass in UM patients (regression coefficient 0.0689, 95% confidence interval 0.0689-0.1123, R2 = 27.1%). CONCLUSIONS: Elevated ME20-S serum levels are associated with tumor size and advanced stages of UM while low levels are characteristic of DF patients. ME20-S might be a promising serum marker for UM and useful for monitoring metastatic disease.

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