Ha Ye Jin, Park Seong-Hwan, Kim Seon-Kyu, Tak Ka Hee, Kim Jeong-Hwan, Kim Chan Wook, Yoon Yong Sik, Kim Seon-Young, Lee Jong Lyul
Asan Institute for Life Sciences, Asan Medical Center, Seoul, 05505, Korea.
Aging Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Daejeon, 34141, Korea.
Sci Data. 2025 Feb 5;12(1):213. doi: 10.1038/s41597-025-04561-4.
Pseudomyxoma peritonei (PMP), a rare condition characterized by mucinous ascites in the peritoneal cavity, often leads to a poor prognosis. However, omics profiling of this disease remains significantly underexplored. Here, we present single-cell transcriptomic profiling of five PMP cases to identify cell type-specific gene features associated with PMP pathogenesis. Additionally, we provide bulk RNA-seq datasets from two independent cohorts: 19 fresh frozen tissue samples (12 PMPs) and 34 formalin-fixed paraffin-embedded (FFPE) samples (25 PMPs). We also offer protein expression data from a tissue microarray (TMA) analysis of 90 samples (45 PMPs). Our single-cell and bulk transcriptomic profiles, along with TMA verifications, reveal the cellular diversity of PMP, highlighting the coexistence of epithelial and mesenchymal characteristics within PMP cells. These datasets enhance our understanding of PMP pathogenesis and provide a valuable resource for uncovering the intricate molecular landscape of PMP, with the potential to improve clinical utility through further research.
腹膜假黏液瘤(PMP)是一种罕见疾病,其特征为腹腔内出现黏液性腹水,通常预后较差。然而,对这种疾病的组学分析仍未得到充分探索。在此,我们展示了5例PMP的单细胞转录组分析结果,以确定与PMP发病机制相关的细胞类型特异性基因特征。此外,我们还提供了来自两个独立队列的批量RNA测序数据集:19个新鲜冷冻组织样本(12个PMP样本)和34个福尔马林固定石蜡包埋(FFPE)样本(25个PMP样本)。我们还提供了对90个样本(45个PMP样本)进行组织微阵列(TMA)分析得到的蛋白质表达数据。我们的单细胞和批量转录组图谱,以及TMA验证,揭示了PMP的细胞多样性,突出了PMP细胞中上皮和间充质特征的共存。这些数据集加深了我们对PMP发病机制的理解,并为揭示PMP复杂的分子景观提供了宝贵资源,有望通过进一步研究提高临床应用价值。