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The extent of whole‐genome copy number alterations predicts aggressive features in primary melanomas
Authors:Greta Gandolfi  Caterina Longo  Elvira Moscarella  Iris Zalaudek  Valentina Sancisi  Margherita Raucci  Gloria Manzotti  Mila Gugnoni  Simonetta Piana  Giuseppe Argenziano  Alessia Ciarrocchi
Affiliation:1. Laboratory of Translational Research, Arcispedale S. Maria Nuova‐IRCCS, Reggio Emilia, Italy;2. Skin Cancer Unit, Arcispedale Santa Maria Nuova‐IRCCS, Reggio Emilia, Italy;3. Department of Dermatology and Venerology, Non‐Melanoma Skin Cancer Unit, Medical University of Graz, Graz, Austria;4. Pathology Unit, Arcispedale S. Maria Nuova‐IRCCS, Reggio Emilia, Italy;5. Dermatology Unit, Second University of Naples, Naples, Italy
Abstract:Recent evidence indicates that melanoma comprises distinct types of tumors and suggests that specific morphological features may help predict its clinical behavior. Using a SNP‐array approach, we quantified chromosomal copy number alterations (CNA) across the whole genome in 41 primary melanomas and found a high degree of heterogeneity in their genomic asset. Association analysis correlating the number and relative length of CNA with clinical, morphological, and dermoscopic attributes of melanoma revealed that features of aggressiveness were strongly linked to the overall amount of genomic damage. Furthermore, we observed that melanoma progression and survival were mainly affected by a low number of large chromosome losses and a high number of small gains. We identified the alterations most frequently associated with aggressive melanoma, and by integrating our data with publicly available gene expression profiles, we identified five genes which expression was found to be necessary for melanoma cells proliferation. In conclusion, this work provides new evidence that the phenotypic heterogeneity of melanoma reflects a parallel genetic diversity and lays the basis to define novel strategies for a more precise prognostic stratification of patients.
Keywords:primary melanoma  aggressiveness  copy number alterations  whole‐genome SNP array  dermoscopy
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