Peng Rui, Zhang Guohong, Li Hang
Department of Dermatology, Peking University First Hospital, National Clinical Research Center for Skin and Immune Diseases, Beijing Key Laboratory of Molecular Diagnosis on Dermatoses, NMPA Key Laboratory for Quality Control and Evaluation of Cosmetics, Beijing, China.
Division of Pathology, Shantou University Medical College, Shantou, Guangdong.
Dermatol Surg. 2023 May 1;49(5S):S27-S33. doi: 10.1097/DSS.0000000000003771. Epub 2023 Mar 30.
Dermatofibrosarcoma protuberans (DFSP) is a cutaneous sarcoma with obscure origin and multidirectional differentiation. Application of RNA-Seq in the detection of COL1A1-PDGFB is still at early stages.
We aim to test the efficacy of fusion gene detection using bulk RNA-Seq in DFSPs, explore altered molecular pathways and biological processes for evidences of tumor origin and cell identity shift.
Dermatofibrosarcoma protuberans and normal dermis samples were acquired for RNA-Seq. Fusion gene detection was performed using STAR-Fusion. RNA-Seq 2G yielded differentially expressed genes. Altered pathways, key gene ontology terms, and similar cell/tissue types were identified with gene set enrichment analysis. xCell was used for cell types enrichment analysis.
28/30 CD34(+) cases were positive for COL1A1-PDGFB. 406 upregulated and 543 downregulated genes were determined. Among the top 10 upregulated genes, 6 had neural distribution, function, or disease correlation. The upregulated genes were related to synapse, trans-synaptic signaling, neural development, and extracellular matrix. Similarities between DFSP and nervous system components were highlighted, with fibroblast cellular abundancy increased during xCell analysis.
Bulk RNA-Seq provided with high detection rate of COL1A1-PDGFB. Dermatofibrosarcoma protuberans showed fibroblastic activity and neural features, which validated DFSP's fibroblast origin and tendency of neural differentiation.
隆突性皮肤纤维肉瘤(DFSP)是一种起源不明且具有多向分化的皮肤肉瘤。RNA测序在检测COL1A1-PDGFB方面的应用仍处于早期阶段。
我们旨在测试使用批量RNA测序检测DFSP中融合基因的功效,探索改变的分子途径和生物学过程,以寻找肿瘤起源和细胞身份转变的证据。
获取隆突性皮肤纤维肉瘤和正常真皮样本进行RNA测序。使用STAR-Fusion进行融合基因检测。RNA测序2G产生差异表达基因。通过基因集富集分析确定改变的途径、关键基因本体术语以及相似的细胞/组织类型。使用xCell进行细胞类型富集分析。
30例CD34(+)病例中有28例COL1A1-PDGFB呈阳性。确定了406个上调基因和543个下调基因。在前10个上调基因中,有6个与神经分布、功能或疾病相关。上调基因与突触、跨突触信号传导、神经发育和细胞外基质有关。突出显示了DFSP与神经系统成分之间的相似性,在xCell分析期间成纤维细胞丰度增加。
批量RNA测序对COL1A1-PDGFB的检测率很高。隆突性皮肤纤维肉瘤表现出成纤维细胞活性和神经特征,这证实了DFSP的成纤维细胞起源和神经分化倾向。