Olson Center for Women's Health, Department of Obstetrics and Gynecology, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Veterans Affairs Nebraska Western Iowa Health Care System, Omaha, NE 68105, USA.
Endocrinology. 2024 Jul 1;165(8). doi: 10.1210/endocr/bqae074.
Uterine leiomyoma or fibroids are prevalent noncancerous tumors of the uterine muscle layer, yet their origin and development remain poorly understood. We analyzed RNA expression profiles of 15 epigenetic mediators in uterine fibroids compared to myometrium using publicly available RNA sequencing (RNA-seq) data. To validate our findings, we performed RT-qPCR on a separate cohort of uterine fibroids targeting these modifiers confirming our RNA-seq data. We then examined protein profiles of key N6-methyladenosine (m6A) modifiers in fibroids and their matched myometrium, showing no significant differences in concordance with our RNA expression profiles. To determine RNA modification abundance, mRNA and small RNA from fibroids and matched myometrium were analyzed by ultra-high performance liquid chromatography-mass spectrometry identifying prevalent m6A and 11 other known modifiers. However, no aberrant expression in fibroids was detected. We then mined a previously published dataset and identified differential expression of m6A modifiers that were specific to fibroid genetic subtype. Our analysis also identified m6A consensus motifs on genes previously identified to be dysregulated in uterine fibroids. Overall, using state-of-the-art mass spectrometry, RNA expression, and protein profiles, we characterized and identified differentially expressed m6A modifiers in relation to driver mutations. Despite the use of several different approaches, we identified limited differential expression of RNA modifiers and associated modifications in uterine fibroids. However, considering the highly heterogenous genomic and cellular nature of fibroids, and the possible contribution of single molecule m6A modifications to fibroid pathology, there is a need for greater in-depth characterization of m6A marks and modifiers in a larger and diverse patient cohort.
子宫肌瘤或纤维瘤是常见的子宫平滑肌层非癌性肿瘤,但它们的起源和发展仍不清楚。我们分析了 15 种表观遗传调节剂在子宫肌瘤与子宫肌层中的 RNA 表达谱,使用了公开的 RNA 测序 (RNA-seq) 数据。为了验证我们的发现,我们针对这些调节剂在另一个子宫肌瘤队列中进行了 RT-qPCR,证实了我们的 RNA-seq 数据。然后,我们检查了纤维瘤及其匹配的子宫肌层中关键 N6-甲基腺苷 (m6A) 调节剂的蛋白谱,与我们的 RNA 表达谱一致,没有发现明显的差异。为了确定 RNA 修饰丰度,我们通过超高效液相色谱-质谱法分析了纤维瘤和匹配的子宫肌层中的 mRNA 和小 RNA,鉴定出普遍存在的 m6A 和其他 11 种已知修饰物。然而,在纤维瘤中没有检测到异常表达。然后,我们挖掘了一个以前发表的数据集,并确定了特定于纤维瘤遗传亚型的 m6A 调节剂的差异表达。我们的分析还确定了 m6A 共识基序在先前被确定为子宫纤维瘤失调的基因上。总体而言,我们使用最先进的质谱、RNA 表达和蛋白谱分析技术,对与驱动突变相关的 m6A 调节剂进行了特征描述和鉴定。尽管使用了几种不同的方法,但我们仅发现了 RNA 修饰剂在子宫纤维瘤中差异表达有限。然而,考虑到纤维瘤的基因组和细胞性质高度异质,以及单个分子 m6A 修饰对纤维瘤病理学的可能贡献,需要在更大、更多样化的患者队列中对 m6A 标记和修饰物进行更深入的表征。