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具有 PRDM10 融合的未分化多形性肉瘤具有独特的基因表达谱。

Undifferentiated pleomorphic sarcomas with PRDM10 fusions have a distinct gene expression profile.

机构信息

Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.

Department of Pathology and Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden.

出版信息

J Pathol. 2019 Dec;249(4):425-434. doi: 10.1002/path.5326. Epub 2019 Aug 27.

DOI:10.1002/path.5326
PMID:31313299
Abstract

Undifferentiated pleomorphic sarcoma (UPS) is a highly aggressive soft tissue tumor. A subset of UPS is characterized by a CITED2-PRDM10 or a MED12-PRDM10 gene fusion. Preliminary data suggest that these so-called PRDM10-rearranged tumors (PRT) are clinically more indolent than classical high-grade UPS, and hence important to recognize. Here, we assessed the spectrum of accompanying mutations and the gene expression profile in PRT using genomic arrays and sequencing of the genome (WGS) and transcriptome (RNA-seq). The fusion protein's function was further investigated by conditional expression of the CITED2-PRDM10 fusion in a fibroblast cell line, followed by RNA-seq and an assay for transposase-accessible chromatin (ATAC-seq). The CADM3 gene was found to be differentially up-regulated in PRT and cell lines and was also evaluated for expression at the protein level using immunohistochemistry (IHC). The genomic analyses identified few and nonrecurrent mutations in addition to the structural variants giving rise to the gene fusions, strongly indicating that the PRDM10-fusions represent the critical driver mutations. RNA-seq of tumors showed a distinct gene expression profile, separating PRT from high-grade UPS and other soft tissue tumors. CADM3 was among the genes that was consistently and highly expressed in both PRT and fibroblasts expressing CITED2-PRDM10, suggesting that it is a direct target of the PRDM10 transcription factor. This conclusion is in line with sequencing data from ATAC-seq, showing enrichment of PRDM10 binding sites, suggesting that the amino-terminal fusion partner contributes by making the DNA more accessible to PRDM10 binding. © 2019 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

摘要

未分化多形性肉瘤 (UPS) 是一种高度侵袭性的软组织肿瘤。UPS 的一个亚组具有 CITED2-PRDM10 或 MED12-PRDM10 基因融合。初步数据表明,这些所谓的 PRDM10 重排肿瘤 (PRT) 在临床上比经典的高级 UPS 更为惰性,因此识别这些肿瘤很重要。在这里,我们使用基因组芯片和全基因组测序 (WGS) 和转录组测序 (RNA-seq) 评估了 PRT 中伴随突变的谱和基因表达谱。通过在成纤维细胞系中条件表达 CITED2-PRDM10 融合蛋白,进一步研究了融合蛋白的功能,随后进行了 RNA-seq 和转座酶可及染色质 (ATAC-seq) 分析。发现 CADM3 基因在 PRT 和细胞系中差异上调,并使用免疫组织化学 (IHC) 评估了其在蛋白质水平上的表达。基因组分析除了导致基因融合的结构变异外,还发现了很少且非重现性的突变,强烈表明 PRDM10 融合代表关键驱动突变。肿瘤的 RNA-seq 显示出独特的基因表达谱,将 PRT 与高级 UPS 和其他软组织肿瘤区分开来。CADM3 是在 PRT 和表达 CITED2-PRDM10 的成纤维细胞中一致且高度表达的基因之一,这表明它是 PRDM10 转录因子的直接靶标。这一结论与 ATAC-seq 的测序数据一致,表明 PRDM10 结合位点富集,表明氨基末端融合伴侣通过使 DNA更容易被 PRDM10 结合来做出贡献。 © 2019 英国和爱尔兰病理学学会。由 John Wiley & Sons, Ltd. 出版。

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