胶质瘤中多核巨细胞的二态性。

IF 1.2 4区 医学 Q4 MICROSCOPY
Muhi Dean Barazi, John Paul Aboubechara, Muhammad Sulman, Haitham H Maraqah, Mones S Abu-Asab, Han Sung Lee, Orwa Aboud
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引用次数: 0

摘要

广泛的研究已经开始揭示高级别胶质瘤的分子特征。然而,对其发病机制的超微结构理解仍未得到充分探索。多核巨细胞是具有多个核的大细胞,被认为是由多个肿瘤细胞融合形成的。在这项研究中,我们旨在阐明idh1 -野生型胶质母细胞瘤(GBM)和idh1 -突变型星形细胞瘤(4级)中多核巨细胞(MGCs)的性质,通过表征它们的表型、个体发生、形态、患病率、意义以及对肿瘤进展和治疗耐药性的潜在影响。利用透射电子显微镜(TEM),我们检查了30例肿瘤(18例idh1野生型GBMs和12例idh1突变型星形细胞瘤),发现它们具有两种类型的MGCs。1型由多个肿瘤细胞融合形成。2型似乎是由充满中间丝(IF)和脂质的肿瘤纤维细胞通过两个过程产生的,要么是细胞融合,要么是裸核迁移到一个更大的充满中间丝的肿瘤细胞。我们的研究结果显示,在43%的病例中,MGCs大量存在,这比之前认为的要少。这两种MGC类型在两种胶质瘤中单独或联合发生。此外,MGCs表现为非增殖性;因此,它们对肿瘤发生和增殖的贡献尚未完全解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The dimorphism of the multinucleated giant cells of gliomas.

Extensive research has begun to uncover the molecular characteristics of high grade gliomas. However, an ultrastructural understanding of their pathogenesis remains largely unexplored. Multinucleated giant cells are large cells with multiple nuclei thought to form from the fusion of multiple neoplastic cells. In this study, we aim to elucidate the nature of the multinucleated giant cells (MGCs) within IDH1-wild type glioblastoma (GBM) and IDH1-mutant astrocytoma, grade 4, by characterizing their phenotypes, ontogenies, morphologies, prevalence, significance, and potential impact on tumor progression and treatment resistance. Utilizing transmission electron microscopy (TEM), we examined 30 tumors (18 IDH1-wild type GBMs and 12 IDH1-mutant astrocytomas) and found that they share two types of MGCs. Type 1 is formed by the fusion of several tumor cells. Type 2 seems to be produced by tumor fibrillar cells filled with intermediate filaments (IF) and lipids through two processes, either by cell fusion or by the immigration of naked nuclei to a larger IF-filled tumor cell. Our results showed that MGCs are abundantly present in 43% of cases, making them less rare than previously believed. The two MGC types occurred solely or in combination in both types of gliomas. Furthermore, MGCs appear non-proliferative; and therefore, their contribution to tumorigenesis and proliferation is not yet fully resolved.

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来源期刊
Ultrastructural Pathology
Ultrastructural Pathology 医学-病理学
CiteScore
2.00
自引率
10.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: Ultrastructural Pathology is the official journal of the Society for Ultrastructural Pathology. Published bimonthly, we are the only journal to be devoted entirely to diagnostic ultrastructural pathology. Ultrastructural Pathology is the ideal journal to publish high-quality research on the following topics: Advances in the uses of electron microscopic and immunohistochemical techniques Correlations of ultrastructural data with light microscopy, histochemistry, immunohistochemistry, biochemistry, cell and tissue culturing, and electron probe analysis Important new, investigative, clinical, and diagnostic EM methods.
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