浆液性液体
子宫内膜癌
浆液性癌
细胞
癌
生物
清除单元格
病态的
癌症研究
发病机制
子宫内膜
转录组
疾病
起源细胞
癌症
病理
基因
医学
卵巢癌
遗传学
免疫学
内分泌学
基因表达
作者
Andrea Flesken‐Nikitin,Matalin G. Pirtz,Christopher S. Ashe,Lora H. Ellenson,Anna Yemelyanova,Benjamin D. Cosgrove,Alexander Yu. Nikitin
摘要
Serous endometrial carcinoma (SEC) is one of the most lethal types of uterine cancer, responsible for about 40% of all endometrial cancer-related deaths. Cell state dynamics during the early stages of SEC remain largely unknown, thereby hindering early detection and treatment of this disease. Here, we provide a comprehensive census of cell types and their states for normal, predysplastic, and dysplastic endometrium in a genetic mouse model of SEC. We report that predysplastic changes are characterized by increasingly diverse immature luminal epithelial cell populations. The decrease in differentiated cell states is accompanied by the emergence of a 'single-cell and spatial transcriptome dysregulation' gene signature. This signature contains seven genes that predict poor patient prognosis and are promising diagnostic markers and therapeutic targets. In summary, our results suggest an important role of the luminal epithelial cell state in SEC pathogenesis and validate our mouse SEC model as a capable comparative platform for preclinical studies. © 2025 The Pathological Society of Great Britain and Ireland.
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