Inhibition of lysine-specific histone demethylase 1A suppresses adenomyosis through reduction in ectopic endometrial stromal cell proliferation, migration, and invasion.

IF 2.5 4区 医学 Q2 PATHOLOGY Cytojournal Pub Date : 2024-11-22 eCollection Date: 2024-01-01 DOI:10.25259/Cytojournal_48_2024
Limei Cui, Changmei Sang, Ruoqing Li, Shuping Zhao
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Abstract

Objective: Deep endometriosis is now referred to as adenomyosis externa, whereas adenomyosis is once known as endometriosis interna. Lysine-specific histone demethylase 1A (KDM1A, commonly LSD1) is a lysine demethylase that targets histone and non-histone proteins. This study aimed to assess how KDM1A affects the migration, invasion, and proliferation of adenomyosis-derived endometrial stromal cells (ESCs).

Material and methods: Immunocytochemistry staining was used to identify primary ectopic endometrial stromal cells (EESCs) and eutopic endometrial stromal cells (EuESCs) were isolated and purified from patients with complete hysterectomy for adenomyosis. Cell counting kit-8 assay, colony formation, wound scratch, and transwell assays were used to investigate the effect of silencing KDM1A on the inhibition cell viability, colony, migration, and invasion, respectively. Mechanistic investigations were carried out by Western blot and quantitative real-time polymerase chain reaction (qRT-PCR).

Results: Vimentin staining was highly positive and cytokeratin staining was nearly negative in EESCs and EuESCs. KDM1A silencing reduced the ability of EESCs and EuESCs to proliferate (P < 0.001). The proliferation, motility, and invasiveness of EESCs and EuESCs were markedly reduced when KDM1A was silenced (P < 0.001). KDM1A silencing substantially downregulated invasion- and migration-related proteins or genes according to Western blot and qRT-PCR analysis (P < 0.05). EESCs and EuESCs with KDM1A silencing showed a higher reduction in these proteins than the control group (P < 0.05).

Conclusion: In adenomyosis, silencing KDM1A can limit the motility, invasiveness, and proliferation of EuESCs and EESCs. These outcomes could potentially correlate with the decreased expression levels of matrix metalloproteinases (MMP)-2, MMP-9, Fascin, and Erzin proteins.

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抑制赖氨酸特异性组蛋白去甲基化酶1A通过减少异位子宫内膜基质细胞的增殖、迁移和侵袭来抑制子宫腺肌症。
目的:深部子宫内膜异位症现在被称为子宫腺肌症外部,而子宫腺肌症曾经被称为内部子宫内膜异位症。赖氨酸特异性组蛋白去甲基化酶1A (KDM1A,通常为LSD1)是一种针对组蛋白和非组蛋白的赖氨酸去甲基化酶。本研究旨在评估KDM1A如何影响腺肌病源性子宫内膜基质细胞(ESCs)的迁移、侵袭和增殖。材料和方法:采用免疫细胞化学染色法鉴定原发性异位子宫内膜基质细胞(EESCs),并从子宫腺肌症全子宫切除术患者中分离纯化异位子宫内膜基质细胞(EuESCs)。采用细胞计数试剂盒-8法、菌落形成法、伤口划伤法和transwell法分别研究沉默KDM1A对抑制细胞活力、菌落、迁移和侵袭的影响。采用Western blot和定量实时聚合酶链反应(qRT-PCR)进行机制研究。结果:在EESCs和EuESCs中,波形蛋白染色呈高阳性,细胞角蛋白染色接近阴性。KDM1A沉默降低了eesc和euesc的增殖能力(P < 0.001)。KDM1A沉默后,EESCs和EuESCs的增殖、活力和侵袭性明显降低(P < 0.001)。Western blot和qRT-PCR分析显示,KDM1A沉默显著下调侵袭和迁移相关蛋白或基因(P < 0.05)。与对照组相比,KDM1A沉默的EESCs和EuESCs中这些蛋白的减少幅度更大(P < 0.05)。结论:在子宫腺肌症中,沉默KDM1A可限制EuESCs和EESCs的运动、侵袭性和增殖。这些结果可能与基质金属蛋白酶(MMP)-2、MMP-9、Fascin和Erzin蛋白表达水平的降低有关。
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来源期刊
Cytojournal
Cytojournal PATHOLOGY-
CiteScore
2.20
自引率
42.10%
发文量
56
审稿时长
>12 weeks
期刊介绍: The CytoJournal is an open-access peer-reviewed journal committed to publishing high-quality articles in the field of Diagnostic Cytopathology including Molecular aspects. The journal is owned by the Cytopathology Foundation and published by the Scientific Scholar.
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