黄体酮在idh突变型星形细胞瘤中的临床病理作用。

Q3 Medicine
Journal of Microscopy and Ultrastructure Pub Date : 2023-06-02 eCollection Date: 2025-04-01 DOI:10.4103/jmau.jmau_115_22
Eman Ahmed Abd Elmaogod, Dina Ahmed Khairy, Abla Sayed Mahmoud
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引用次数: 0

摘要

背景:性类固醇激素可影响星形细胞瘤,这是最常见的神经胶质瘤。黄体酮(P)可能参与癌症的发展。本研究评估了49例(异柠檬酸脱氢酶(IDH)突变体)星形细胞瘤中孕激素受体(PR)的表达及其增殖潜能。目的:本研究旨在评估免疫组织化学孕酮在idh突变型星形细胞肿瘤中的表达,并将其与肿瘤病理参数进行关联。背景和设计:这是一项回顾性观察性横断面研究。材料和方法:采用组织病理学和免疫组织化学方法对49例颅内星形细胞瘤标本进行pr和异柠檬酸脱氢酶(IDH)酶突变检测。结果:女性26例(53.1%),男性23例(46.9%)(n = 49)。中位年龄为41.5岁(27.75岁)。49例idh突变型星形细胞瘤中有42例(85.7%)显示PR免疫反应阳性。27例2级星形细胞瘤(弥漫性)中有20例表达,7例3级星形细胞瘤(间变性)中有7例表达,15例4级星形细胞瘤(胶质母细胞瘤)中有15例表达。肿瘤血管壁及微血管内皮增生细胞PR阳性。此外,与中线肿瘤相比,右侧和左侧肿瘤中PR的表达明显增加,幕上肿瘤中PR的表达明显高于幕下肿瘤。阳性坏死高。肿瘤分级与PR表达呈显著正相关(r = 0.972;P < 0.001),且与患者年龄呈中度正线性相关(r = 0.414;P = 0.003)。复发和性别与PR表达无关。结论:我们认为PR与idh突变星形细胞瘤的组织学分级、生长和血管生成有关。因此,它可以作为一种新的有希望的靶向治疗的预后标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinicopathological Role of Progesterone Hormone in IDH-Mutant Astrocytoma.

Context: Sex steroid hormones can influence astrocytomas, the most common form of glioma. Progesterone (P) may participate in cancer development. The current study evaluated the progesterone receptor (PR) expression in 49 (isocitrate dehydrogenase (IDH) mutant) astrocytomas concerning their proliferative potential.

Aim: The current study aimed to assess the immunohistochemical progesterone expression in IDH-mutant astrocytic tumors besides correlating such expression with the pathological parameters of the tumors.

Settings and design: This is a retrospective observational cross-sectional study.

Materials and methods: Forty-nine intracranial astrocytoma specimens were evaluated for PRs and isocitrate dehydrogenase (IDH) enzyme mutations in a histopathological and immunohistochemical study.

Results: The study included 26 females (53.1%) and 23 males (46.9%) (n = 49). The median age was 41.5 (27.75) years. IDH-mutant astrocytic tumors demonstrated positive PR immunoreactivity in 42 of 49 cases (85.7%). Its expression was observed in 20 of 27 cases of Grade 2 astrocytomas (diffuse type), 7 of 7 cases of Grade 3 astrocytomas (anaplastic type), and 15 of 15 cases of Grade 4 astrocytomas (glioblastoma). In addition, tumor vessel walls and cells with microvascular endothelial proliferation showed PR positivity. Furthermore, there was a significant increase in PR expression in the right and left-sided tumors compared to midline tumors and in supratentorial tumors compared to infratentorial tumors. It was high with positive necrosis. The tumor grade and the expression of PR were strongly positively correlated (r = 0.972; P < 0.001), and there was a moderately positive linear correlation between them and the patient's age (r = 0.414; P = 0.003). Recurrence and gender were not associated with PR expression.

Conclusion: We propose a correlation between PR and the histologic grade, growth, and angiogenesis of the IDH-mutant astrocytoma. As a result, it can act as a prognostic marker for a new promising target therapy.

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