Single-Nucleus Analysis Reveals Tumor Heterogeneity of Aldosterone-Producing Adenoma

生物 癌变 细胞 突变 核糖核酸 人口 遗传学 下调和上调 基因 癌症研究 细胞生物学 医学 环境卫生
作者
Masanori Murakami,Kazunari Hara,Kenji Ikeda,Masato Horino,Rei Okazaki,Yoshihiro Niitsu,A. Takeuchi,Jun Aoki,Kumiko Shiba,Kazutaka Tsujimoto,Chikara Komiya,Yuki Nakamura,Morito Kurata,Takumi Akashi,Yasuhisa Fujii,Tetsuya Yamada
出处
期刊:Hypertension [Lippincott Williams & Wilkins]
卷期号:81 (2): 361-371 被引量:9
标识
DOI:10.1161/hypertensionaha.123.21446
摘要

BACKGROUND: Recent advances in omics techniques have allowed detailed genetic characterization of aldosterone-producing adenoma (APA). The pathogenesis of APA is characterized by tumorigenesis-associated aldosterone synthesis. The pathophysiological intricacies of APAs have not yet been elucidated at the level of individual cells. Therefore, a single-cell level analysis is speculated to be valuable in studying the differentiation process of APA. METHODS: mutation and nonfunctional adenomas obtained from 3 and 2 patients, respectively. RESULTS: The single-nucleus RNA sequencing revealed the intratumoral heterogeneity of APA and identified cell populations consisting of a shared cluster of nonfunctional adenoma and APA. In addition, we extracted 2 cell fates in APA and obtained a cell population specialized in aldosterone synthesis. Genes related to ribosomes and neurodegenerative diseases were upregulated in 1 of these fates, whereas those related to the regulation of glycolysis were upregulated in the other fate. Furthermore, the total RNA reads in the nucleus were higher in hormonally activated clusters, indicating a marked activation of transcription per cell. CONCLUSIONS: -mutated APAs provides the postulation that a heterogeneous process of cellular differentiation was implicated in the pathophysiological mechanisms underlying APA tumors.
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