Aumann K
Institut für Klinische Pathologie, Universitätsklinikum Freiburg, Medizinische Fakultät, Albert-Ludwigs-Universität Freiburg, Breisacher Straße 115a, 79106, Freiburg, Deutschland.
Pathologe. 2018 Dec;39(Suppl 2):199-207. doi: 10.1007/s00292-018-0520-0.
In this work different types of dysregulation of signaling proteins in the context of myeloproliferative neoplasms are examined. In this heterogeneous disease group, uncontrolled cell proliferation plays a crucial role for the initiation of tumorigenesis, which Robert Weinberg described as a "hallmark" for the development of cancer. Protein dysregulation in form of overexpression of GAB2, a protein involved in formation of the CML-pathognomonic BCR/ABL-translocation complex, results in an enhanced disease phenotype in a Bcr/Abl-positive mouse model and disease acceleration is associated with a change of the subcellular localization of GAB2 in human blasts in CML-bone marrow biopsies. Furthermore, analyses of a mouse model show that a protein dysregulation caused by a distinct translocation (Tel-Syk) leads to the formation of a specific and morphologically very characteristic phenotype in the bone marrow of diseased mice. Moreover, results were presented which show that in certain subgroups of Myeloproliferative Neoplasms the protein NFE2, which is initially known only as a translocating factor, is apparently regulated by altering its subcellular localization. The difference in the subcellular localization of NFE2 in erythroid bone marrow cells is so clear between Essential Thrombocythemia and Primary Myelofibrosis that quantitative NFE2 immunohistochemistry can be used as an ancillary tool to diagnostically discriminate these two entities in an early stage.
在这项工作中,研究了骨髓增殖性肿瘤背景下信号蛋白的不同类型失调。在这个异质性疾病组中,不受控制的细胞增殖在肿瘤发生起始过程中起着关键作用,罗伯特·温伯格将其描述为癌症发展的“标志”。GAB2蛋白过表达形式的蛋白质失调,GAB2是一种参与慢性粒细胞白血病特征性BCR/ABL易位复合体形成的蛋白质,在Bcr/Abl阳性小鼠模型中导致疾病表型增强,并且疾病加速与慢性粒细胞白血病骨髓活检中人类原始细胞中GAB2的亚细胞定位改变有关。此外,对一个小鼠模型的分析表明,由一种独特的易位(Tel-Syk)引起的蛋白质失调导致患病小鼠骨髓中形成一种特定的、形态上非常有特征的表型。而且,研究结果表明,在骨髓增殖性肿瘤的某些亚组中,最初仅作为一种易位因子为人所知的蛋白质NFE2显然通过改变其亚细胞定位而受到调控。在真性红细胞增多症和原发性骨髓纤维化之间,红系骨髓细胞中NFE2的亚细胞定位差异非常明显,以至于定量NFE2免疫组化可作为一种辅助工具在早期诊断性区分这两种疾病。