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呼吸链复合体I是嗜酸性细胞瘤的一种线粒体肿瘤抑制因子。

Respiratory chain complex I is a mitochondrial tumor suppressor of oncocytic tumors.

作者信息

Zimmermann Franz A, Mayr Johannes A, Feichtinger Rene, Neureiter Daniel, Lechner Roman, Koegler Christian, Ratschek Manfred, Rusmir Husic, Sargsyan Karine, Sperl Wolfgang, Kofler Barbara

机构信息

Department of Pediatrics, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria.

出版信息

Front Biosci (Elite Ed). 2011 Jan 1;3(1):315-25. doi: 10.2741/e247.

Abstract

Oncocytic tumors, also called oxyphilic tumors, are characterized by hyperproliferation of mitochondria, which histologically presents as a fine granular eosinophilic cytoplasm. In accordance with the high mitochondrial density in oncocytomas, transcript levels of subunits of complexes of the oxidative phosphorylation (OXPHOS) system are increased. Hence, for a long time oncocytomas were presumed to have a highly active aerobic mitochondrial energy metabolism. Recently, detailed analysis of all OXPHOS complexes in a variety of oncocytomas revealed loss of complex I and compensatory up-regulation of the other complexes. In half of the oncocytoma cases examined the absence of complex I is caused by disruptive mutations in mitochondrial DNA encoding complex I subunits. The new data presented here on rare oncocytomas and the accompanying review of the literature clearly indicate that complex I deficiency in combination with up-regulation of mitochondria can be regarded as a hallmark of oncocytic tumor cells. Therefore, complex I of the respiratory chain has to be added to the growing list of mitochondrial tumor suppressors.

摘要

嗜酸性细胞瘤,也称为嗜氧细胞瘤,其特征是线粒体过度增殖,在组织学上表现为细颗粒状嗜酸性细胞质。鉴于嗜酸性细胞瘤中线粒体密度较高,氧化磷酸化(OXPHOS)系统复合物亚基的转录水平会升高。因此,长期以来人们认为嗜酸性细胞瘤具有高度活跃的有氧线粒体能量代谢。最近,对多种嗜酸性细胞瘤中所有OXPHOS复合物的详细分析显示,复合物I缺失,而其他复合物则出现代偿性上调。在一半的被检查嗜酸性细胞瘤病例中,复合物I的缺失是由编码复合物I亚基的线粒体DNA中的破坏性突变引起的。这里呈现的关于罕见嗜酸性细胞瘤的新数据以及相关文献综述清楚地表明,复合物I缺陷与线粒体上调相结合可被视为嗜酸性肿瘤细胞的一个标志。因此,呼吸链的复合物I必须被添加到不断增加的线粒体肿瘤抑制因子列表中。

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