A prospective multicenter cohort study of cutaneous melanoma: clinical staging and potential associations with HIF-1 alpha and VEGF expressions


Por: Martinez-Garcia, MA, Riveiro-Falkenbach, E, Rodriguez-Peralto, JL, Nagore, E, Martorell-Calatayud, A, Campos-Rodriguez, F, Farre, R, Blasco, LH, Roca, JB, Vives, EC, Sanchez-de-la-Torre, A, Capa, JA, Montserrat, JM, Almendros, I, Perez-Gil, A, Nuno, VC, Cano-Pumarega, I, Penafiel, JC, Cambriles, TD, Mediano, O, Arias, JD, Gozal, D

Publicada: 1 dic 2017
Resumen:
Melanoma is a highly prevalent cancer that is associated with substantial mortality. Although clinical staging procedures can serve as relatively robust prognostic indicators, we aimed to determine whether assessments of the abundance of hypoxia inducible factor-1 alpha (HIF-1 alpha) or vascular endothelial growth factor (VEGF) in postexcisional melanoma tumor tissues may enable more accurate determination of tumor aggressiveness. We carried out a multicenter prospective study, in which we systematically evaluated 376 consecutive patients diagnosed with melanoma, and performed histochemical assessments for both HIF-1 alpha and VEGF immunoreactivity in the tumor biopsies. Multivariate analyses showed that higher HIF-1 alpha expression, but not high VEGF, were associated significantly and independently with increased tumor aggressiveness as derived from several well-established aggressiveness criteria. A limitation of this study was that this was a descriptive prospective study lacking a post-hoc verification arm. Thus, the presence of increased numbers of positively labeled HIF-1 alpha cells in melanoma tumors may potentially serve as an indicator of tumor phenotype and prognosis, and accordingly guide therapy. Copyright (C) 2017 Wolters Kluwer Health, Inc. All rights reserved.
ISSN: 09608931





MELANOMA RESEARCH
Editorial
LIPPINCOTT WILLIAMS & WILKINS, TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 27 Número: 6
Páginas: 558-564
WOS Id: 000415743000004
ID de PubMed: 28885396

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