未分化黑色素瘤:一项临床病理和基因表达分析研究,鉴定HMGA2作为诊断标志物。

IF 4.2 1区 医学 Q1 PATHOLOGY
Grant M Fischer, Diogo Maia-Silva, Dora Dias-Santagata, Jason L Hornick, Eleanor Russell-Goldman
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引用次数: 0

摘要

根据定义,未分化黑色素瘤缺乏黑色素细胞标记物S100蛋白、Sox10、mar1和HMB45的表达,这给诊断带来了独特的挑战。尽管存在这种异常表型,未分化黑色素瘤的特征是已知的黑色素瘤驱动改变,包括BRAF和NRAS突变。由于变化的形态学特征和缺乏黑素细胞分化,通常需要分子诊断来识别黑素瘤兼容的驱动改变以支持诊断。在这里,我们描述了一个27个未分化黑色素瘤的队列,并使用基因表达谱来比较未分化黑色素瘤与传统黑色素瘤在相同患者和未匹配病例中出现的匹配病例。未分化黑色素瘤的组织学谱多变,包括上皮样细胞、纺锤状细胞、多形性细胞、横纹肌细胞和球囊细胞,常伴有坏死。值得注意的是,一组未分化的黑色素瘤显示出明显的间质,包括粘液样和血管成分。我们证明,组织学类别是差异基因表达的主要决定因素之间的常规和未分化黑色素瘤。此外,未分化的黑色素瘤显示出几种显著上调的基因表达途径,包括与上皮-间质转化相关的基因表达途径。这些数据为未分化黑色素瘤的转录组表达谱提供了新的见解,并为不寻常的表型提供了潜在的解释。值得注意的是,HMGA2被发现是未分化黑色素瘤队列中最显著的上调基因,免疫组织化学研究表明,HMGA2是诊断未分化黑色素瘤的敏感和特异性标志物,并与表现出重叠形态特征和缺乏黑素细胞分化的模拟瘤区分开来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Undifferentiated Melanoma: A Clinicopathologic and Gene Expression Analysis Study With Identification of HMGA2 as a Diagnostic Marker.

Undifferentiated melanoma poses a unique diagnostic challenge as, by definition, it lacks expression of the melanocytic markers S100 protein, Sox10, Mart1, and HMB45. Despite this aberrant phenotype, undifferentiated melanoma is characterized by known melanoma driver alterations, including BRAF and NRAS mutations. Due to variable morphologic features and a lack of melanocytic differentiation, molecular diagnostics are often required for the identification of melanoma-compatible driver alterations to support the diagnosis. Here, we describe a cohort of 27 undifferentiated melanomas and employ gene expression profiling to compare undifferentiated melanoma to conventional melanoma in both matched cases arising in the same patients and unmatched cases. The histologic spectrum of undifferentiated melanoma was variable and included tumors composed of epithelioid, spindled, pleomorphic, rhabdoid and balloon cells, often with necrosis. Notably, a subset of undifferentiated melanomas demonstrated a prominent stroma, including myxoid and vascular components. We demonstrate that the histologic category is the main determinant of differential gene expression between conventional and undifferentiated melanoma. In addition, undifferentiated melanomas show several significantly upregulated gene expression pathways, including those associated with epithelial-mesenchymal transition. These data provide novel insights into the transcriptomic expression profile of undifferentiated melanoma and offer potential explanations for the unusual phenotype. Notably, HMGA2 was found to be the most significantly up-regulated gene in the undifferentiated melanoma cohort, with immunohistochemical studies demonstrating that HMGA2 is a sensitive and specific marker for the diagnosis of undifferentiated melanoma and for its distinction from mimics which show overlapping morphologic features and lack melanocytic differentiation.

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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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