Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna 40100, Italy.
Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, Bologna 40100, Italy; Dermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna 40100, Italy.
Pathol Res Pract. 2022 Jul;235:153942. doi: 10.1016/j.prp.2022.153942. Epub 2022 May 14.
dysplastic nevi (DN) share some clinical and histological features with melanoma and have been considered intermediate lesions toward malignant transformation. However, scientific evidence of DN representing melanoma precursors is still incomplete, and many observations pointed toward their being a distinct biological entity. The current definition of DN is also confusing and the practical consequence of this uncertainty is the excessive excision of DN with severe atypia. MicroRNAs (miRNAs) are small RNAs that regulate gene expression and whose global expression can classify normal and pathological tissues.
given these considerations, we decided to perform a small RNA profiling study in a group of DN and invasive melanomas obtained from the same patient, to assess tumor evolution according to the global microRNA expression.
we performed a small-RNA sequencing of 6 DN, 2 congenital nevi and 4 cutaneous melanomas obtained from 4 subjects and evaluated the global miRNA expression correlation between samples.
the hierarchical clustering and principal component analyses of global miRNA expression, independently grouped together DN and their matching congenital nevi and showed a divergence of DN miRNA profile from melanoma. Our study suggests that DN have a peculiar and different miRNA expression profile compared to melanomas developed in the same patient, thus supporting the hypothesis that DN are distinct biological entities and not melanoma precursors.
发育不良痣(DN)与黑色素瘤具有一些临床和组织学特征,被认为是向恶性转化的中间病变。然而,DN 代表黑色素瘤前体的科学证据仍然不完整,许多观察结果表明它们是一种独特的生物实体。目前的 DN 定义也令人困惑,这种不确定性的实际后果是严重异型性的 DN 过度切除。microRNAs(miRNAs)是调节基因表达的小 RNA,其整体表达可以对正常和病理组织进行分类。
鉴于这些考虑,我们决定对来自同一患者的一组 DN 和侵袭性黑色素瘤进行小 RNA 谱分析,根据整体 microRNA 表达评估肿瘤的演变。
我们对 4 名患者的 6 个 DN、2 个先天性痣和 4 个皮肤黑色素瘤进行了小 RNA 测序,并评估了样品之间的整体 miRNA 表达相关性。
整体 miRNA 表达的层次聚类和主成分分析,独立地将 DN 及其匹配的先天性痣归为一组,并显示 DN miRNA 谱与黑色素瘤的分离。我们的研究表明,DN 的 miRNA 表达谱与同一患者中发生的黑色素瘤不同,因此支持了 DN 是独特的生物实体而不是黑色素瘤前体的假说。