Stockwin Luke H
Unaffiliated, Frederick, Maryland.
PeerJ. 2020 Jun 19;8:e9394. doi: 10.7717/peerj.9394. eCollection 2020.
Alveolar soft-part sarcoma (ASPS) is an extremely rare malignancy characterized by the unbalanced translocation der(17)t(X;17)(p11;q25). This translocation generates a fusion protein, ASPL-TFE3, that drives pathogenesis through aberrant transcriptional activity. Although considerable progress has been made in identifying ASPS therapeutic vulnerabilities (e.g., MET inhibitors), basic research efforts are hampered by the lack of appropriate in vitro reagents with which to study the disease. In this report, previously unmined microarray data for the ASPS cell line, ASPS-1, was analyzed relative to the NCI sarcoma cell line panel. These data were combined with meta-analysis of pre-existing ASPS patient microarray and RNA-seq data to derive a platform-independent ASPS transcriptome. Results demonstrated that ASPS-1, in the context of the NCI sarcoma cell panel, had some similarities to normal mesenchymal cells and connective tissue sarcomas. The cell line was characterized by high relative expression of transcripts such as , , and Notably, ASPS-1 lacked mRNA expression of myogenesis-related factors , , , , and Furthermore, ASPS-1 had a predicted mRNA surfaceome resembling an undifferentiated mesenchymal stromal cell through expression of , (), (), (), (), (), (), (), (), (), (), (), (), (), (), (), and (). Subsequent re-analysis of ASPS patient data generated a consensus expression profile with considerable overlap between studies. In common with ASPS-1, elevated expression was noted for , , , , , , , , , and . Transcripts over-expressed only in ASPS patient samples included , , , , , and These observations are consistent with that expected for a mesenchymal progenitor cell with adipogenic, osteogenic, or chondrogenic potential. In summary, the consensus data generated in this study highlight the unique and highly conserved nature of the ASPS transcriptome. Although the ability of the ASPL-TFE3 fusion to perturb mRNA expression must be acknowledged, the prevailing ASPS transcriptome resembles that of a mesenchymal stromal progenitor.
肺泡软组织肉瘤(ASPS)是一种极为罕见的恶性肿瘤,其特征为17号染色体衍生染色体der(17)t(X;17)(p11;q25)的不平衡易位。这种易位产生一种融合蛋白ASPL-TFE3,它通过异常转录活性驱动发病机制。尽管在确定ASPS的治疗靶点(如MET抑制剂)方面已取得相当大的进展,但基础研究工作因缺乏合适的体外试剂来研究该疾病而受到阻碍。在本报告中,相对于NCI肉瘤细胞系面板,分析了ASPS细胞系ASPS-1以前未挖掘的微阵列数据。这些数据与对已有的ASPS患者微阵列和RNA测序数据的荟萃分析相结合,以得出一个与平台无关的ASPS转录组。结果表明,在NCI肉瘤细胞系面板的背景下,ASPS-1与正常间充质细胞和结缔组织肉瘤有一些相似之处。该细胞系的特征是某些转录本如 、 、 和 有较高的相对表达。值得注意的是,ASPS-1缺乏与肌生成相关因子 、 、 、 、 和 的mRNA表达。此外,通过 、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )、 ( )和 ( )的表达,ASPS-1的预测mRNA表面组类似于未分化的间充质基质细胞。随后对ASPS患者数据的重新分析产生了一个共识表达谱,各研究之间有相当大的重叠。与ASPS-1一样, 、 、 、 、 、 、 、 、 、 和 的表达升高。仅在ASPS患者样本中过度表达的转录本包括 、 、 、 、 、 和 。这些观察结果与具有成脂、成骨或成软骨潜能的间充质祖细胞的预期一致。总之,本研究中产生的共识数据突出了ASPS转录组独特且高度保守的性质。尽管必须承认ASPL-TFE3融合体干扰mRNA表达的能力,但普遍的ASPS转录组类似于间充质基质祖细胞的转录组。