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

Undifferentiated Melanoma: A Clinicopathologic and Gene Expression Analysis Study With Identification of HMGA2 as a Diagnostic Marker.

作者信息

Fischer Grant M, Maia-Silva Diogo, Dias-Santagata Dora, Hornick Jason L, Russell-Goldman Eleanor

机构信息

Department of Pathology, Brigham and Women's Hospital.

Department of Pathology, Massachusetts General Hospital and Harvard Medical School.

出版信息

Am J Surg Pathol. 2025 Jul 9. doi: 10.1097/PAS.0000000000002452.

Abstract

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.

摘要

未分化黑色素瘤带来了独特的诊断挑战,因为根据定义,它缺乏黑素细胞标志物S100蛋白、Sox10、Mart1和HMB45的表达。尽管存在这种异常表型,但未分化黑色素瘤的特征是具有已知的黑色素瘤驱动改变,包括BRAF和NRAS突变。由于形态特征多样且缺乏黑素细胞分化,通常需要进行分子诊断来识别与黑色素瘤兼容的驱动改变以支持诊断。在此,我们描述了一组27例未分化黑色素瘤,并采用基因表达谱分析,在同一患者出现的匹配病例和不匹配病例中,将未分化黑色素瘤与传统黑色素瘤进行比较。未分化黑色素瘤的组织学谱各不相同,包括由上皮样、梭形、多形性、横纹肌样和气球样细胞组成的肿瘤,常伴有坏死。值得注意的是,一部分未分化黑色素瘤表现出显著的间质,包括黏液样和血管成分。我们证明组织学类别是传统黑色素瘤和未分化黑色素瘤之间差异基因表达的主要决定因素。此外,未分化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,并为其异常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上调最显著的基因,免疫组化研究表明,HMGA2是诊断未分化黑色素瘤及其与形态特征重叠且缺乏黑素细胞分化的模仿病变鉴别的敏感和特异标志物。

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