Comparative survey of mitochondrial ultrastructure in IDH1-mutant astrocytoma and IDH1-wildtype glioblastoma (GBM).

IF 1.1 4区 医学 Q4 MICROSCOPY Ultrastructural Pathology Pub Date : 2023-02-25 DOI:10.1080/01913123.2023.2175942
Haitham H Maraqah, Mones S Abu-Asab, Han Sung Lee, Orwa Aboud
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Abstract

Gliomas are the most common malignant brain tumors with poor prognosis. The WHO's classification recognizes isocitrate dehydrogenase 1 (IDH1) mutant astrocytoma and IDH1-wildtype glioblastoma (GBM). The IDH1 mutation confers a survival advantage over the wildtype. There are several explanations for the metabolic advantage of the IDH1 mutation, some involve mitochondrial implications. Since an ultrastructural comparison of both tumor genotypes is still lacking, we surveyed the ultrastructural effects of the IDH1 mutation on the mitochondria of the IDH1-mutant astrocytoma (n = 15) and IDH1-wildtype glioblastoma (n = 15) tumors. Our results show that both IDH1 genotypes have degenerate and uncoupled mitochondria; this has not been reported before. The presence of ample lipid inclusions and lipid droplets in the cytoplasm of both genotypes support our conclusion of dysfunctional uncoupled mitochondria. Thus, the IDH1 mutation may have no ultrastructural consequences on the mitochondria, and the aberrant mitochondria in both genotypes may be the result of other unknown mutations. The status of the mitochondria in these genotypes portends a clinical challenge since tumor cells with uncoupled mitochondria are more primitive, aggressive, and considerably treatment resistant.

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IDH1突变星形细胞瘤和IDH1野生型胶质母细胞瘤(GBM)线粒体超微结构的比较研究。
胶质瘤是最常见的恶性脑肿瘤,预后较差。世卫组织的分类方法承认异柠檬酸脱氢酶 1(IDH1)突变型星形细胞瘤和 IDH1 野生型胶质母细胞瘤(GBM)。与野生型相比,IDH1 突变具有生存优势。IDH1 突变的代谢优势有多种解释,其中一些涉及线粒体的影响。由于目前还缺乏两种肿瘤基因型的超微结构比较,我们调查了 IDH1 突变对 IDH1 突变星形细胞瘤(n = 15)和 IDH1 野生型胶质母细胞瘤(n = 15)线粒体的超微结构影响。我们的研究结果表明,这两种 IDH1 基因型的线粒体都发生了退化和解偶联;这在以前从未报道过。两种基因型的细胞质中都存在大量的脂质内含物和脂滴,这支持了我们关于未耦合线粒体功能失调的结论。因此,IDH1 突变可能不会对线粒体造成超微结构上的影响,两种基因型的线粒体异常可能是其他未知突变的结果。这些基因型中线粒体的状况预示着临床挑战,因为线粒体未耦合的肿瘤细胞更原始、更具侵袭性,而且对治疗有相当大的耐药性。
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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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