DNA methylation profiles in primary cutaneous melanomas are associated with clinically significant pathologic features. (14th July 2014)

• Record Type: Journal Article
• Authors: Thomas, Nancy E.; Slater, Nathaniel A.; Edmiston, Sharon N.; Zhou, Xin; Kuan, Pei‐Fen; Groben, Pamela A.; Carson, Craig C.; Hao, Honglin; Parrish, Eloise; Moschos, Stergios J.; Berwick, Marianne; Ollila, David W.; Conway, Kathleen
• Is Part Of: Pigment cell & melanoma research. Volume 27:Number 6(2014:Nov.)
• Page Start: 1097
• Page End: 1105
• Publication Date: 2014-07-14
• Subjects: Melanoma -- Periodicals; Chromatophores -- Periodicals; Animal pigments -- Periodicals; 616.99477
• DOI: 10.1111/pcmr.12289
• Languages: English
• ISSNs: 1755-1471

Abstract

<abstract abstract-type="main" id="pcmr12289-abs-0001"> <title>Summary</title> <p>DNA methylation studies have elucidated a methylation signature distinguishing primary melanomas from benign nevi and provided new insights about genes that may be important in melanoma development. However, it is unclear whether methylation differences among primary melanomas are related to tumor pathologic features with known clinical significance. We utilized the Illumina GoldenGate Cancer Panel array to investigate the methylation profiles of 47 primary cutaneous melanomas. Arraywide methylation patterns revealed a positive association of methylation with Breslow thickness and mutated <italic>BRAF</italic>, a negative association with mitotic rate, and a weak association with ulceration. Hierarchical clustering on CpG sites exhibiting the most variable methylation (n = 235) divided the melanoma samples into three clusters, including a highly methylated cluster that was positively associated with Breslow thickness and an intermediately methylated cluster associated with Breslow thickness and mitotic rate. Our findings provide support for the existence of methylation‐defined subsets in melanomas with increased methylation associated with Breslow thickness.</p> </abstract>