Department of Pathology, Amsterdam University Medical Center-Location AMC, University of Amsterdam, Amsterdam, The Netherlands.
Department of Anatomical Pathology, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia.
Eur J Med Res. 2023 Oct 20;28(1):449. doi: 10.1186/s40001-023-01436-5.
Episodic growth due to microvascular proliferations (MVP) has been reported in congenital arteriovenous malformations (AVM), which are normally quiescent lesions composed of mature malformed vessels. Since AVM also may worsen under conditions of hormonal dysregulation, we hypothesized that hormonal influences may stimulate this process of vasoproliferative growth through potential interactions with hormone receptors (HR).
13 Cases of AVM tissue with histologically documented vasoproliferative growth were analyzed quantitatively for the presence and tissue localization of estrogen receptor (ER), progesterone receptor (PGR), growth hormone receptor (GHR) and follicle-stimulating hormone receptor (FSHR) in relation to resident cells of interest (endothelial cells (EC), smooth muscle cells (SMC) and mast cells (MC)) by applying multiplex immunohistochemistry (IHC) staining. Expression patterns in lesions with MVP and mature vessels were quantified and compared. Available fresh frozen tissues of 3 AVM samples were used to confirm the presence of HR using Reverse-Transcriptase quantitative Polymerase Chain Reaction (RT-qPCR).
All four HR studied were expressed in all cases within EC and SMC in areas of MVP and mature vessels, but not in normal skin tissue. ER, GHR, and FSHR showed more expression in EC of MVP and in SMC of mature vessels. RT-qPCR confirmed presence of all 4 HR in both areas.
Expression of ER, PGR, GHR, and FSHR in vasoproliferative areas of congenital AVM could explain onset of sudden symptomatic growth, as has observed in a subpopulation of patients. These findings may have implications for eventual anti-hormonal targeted therapy in the lesions involved.
微脉管增生(MVP)引起的间歇性生长已在先天性动静脉畸形(AVM)中报道,AVM 通常是由成熟畸形血管组成的静止性病变。由于 AVM 也可能在激素失调的情况下恶化,我们假设激素影响可能通过与激素受体(HR)的潜在相互作用刺激这种血管增殖生长过程。
通过应用多重免疫组织化学(IHC)染色,分析了 13 例具有组织学记录的 MVP 组织中雌激素受体(ER)、孕激素受体(PGR)、生长激素受体(GHR)和促卵泡激素受体(FSHR)的存在及其与感兴趣的固有细胞(内皮细胞(EC)、平滑肌细胞(SMC)和肥大细胞(MC))的组织定位。定量分析 MVP 和成熟血管病变中的表达模式并进行比较。使用 3 个 AVM 样本的新鲜冷冻组织,通过逆转录定量聚合酶链反应(RT-qPCR)来证实 HR 的存在。
在所研究的所有 4 种 HR 中,在 MVP 和成熟血管的区域内的 EC 和 SMC 中,所有病例均有表达,但在正常皮肤组织中没有表达。ER、GHR 和 FSHR 在 MVP 的 EC 和成熟血管的 SMC 中表达更多。RT-qPCR 证实了这两种区域中所有 4 种 HR 的存在。
在先天性 AVM 的血管增殖区域中表达 ER、PGR、GHR 和 FSHR,可以解释在一部分患者中观察到的突发性症状性生长的发生。这些发现可能对涉及病变的最终抗激素靶向治疗具有重要意义。