原发性醛固酮增多症
转录组
生物
增生
醛固酮
系统发育树
基因表达谱
继发性高血压
基因
病理
遗传学
内科学
内分泌学
基因表达
医学
血压
作者
Yinjie Gao,Yu Wang,Yue Zhou,Xiaoyan Chang,Yushi Zhang,Min Nie,Anli Tong
出处
期刊:Hypertension
[Lippincott Williams & Wilkins]
日期:2024-11-06
卷期号:82 (1): 96-105
被引量:3
标识
DOI:10.1161/hypertensionaha.124.23398
摘要
BACKGROUND: Primary aldosteronism is predominantly caused by excessive aldosterone production from the adrenal cortex, and the aldosterone-producing structures could take many forms, like adenomas, nodules, micronodules, and so on. Most studies of primary aldosteronism were limited to the hotspot driver genes responsible for autonomous aldosterone production; however, the panoramic genetic architecture and genomic alterations of aldosterone-producing structures and their adjacent hyperplasia glands remain unknown. METHODS: In this study, whole-exome sequencing and transcriptome sequencing (RNA-seq) analyses were performed using functional nodules and matched hyperplasia tissues, which were microdissected guided by aldosterone synthase immunohistochemistry. Phylogenetic trees were constructed based on the shared and unique mutations, gene mutation spectrums, and clonal characteristics. RESULTS: ) were only observed in functional nodules and indicated almost the largest values of cancer cell fraction. Moreover, the functional nodules also harbored some potential variants related to cell proliferation, which were not detected in hyperplasia tissues. Transcriptome analysis suggested that only 25.5% upregulated and 23.3% downregulated genes overlapped between functional nodules and hyperplasia tissues. CONCLUSIONS: This study demonstrated a genetic and transcriptome landscape of aldosterone-producing structures and adjacent hyperplasia glands in primary aldosteronism. The results indicated independent clonal origins on functional nodules and hyperplasia tissues, and little mutual evolutionary relationship was found on their phylogenetic trees.
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