Development of a novel treatment by inhibition of mast cell-associated proteins in neurofibroma tumours

Impact Pub Date : 2023-09-21 DOI:10.21820/23987073.2023.3.40
Misa Yamamoto
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Abstract

Neurofibromatosis type 1 (NF1), also known as von Recklinghausen's disease, is an inherited disorder that will (with high probability) lead to multiple benign tumors in the future. There are several types of NF1 tumors and there is no way to control their incidence other than surgical resection. Associate Professor Misa Yamamoto, an expert in regenerative medicine, is currently conducting a project to elucidate the tumor growth mechanism in NF1 patients. This will lead to the development of innovative treatments for this disease. The researchers are affiliated with the Department of Clinical Laboratory Sciences, Graduate School of Medicine, Yamaguchi University, Japan. Currently, we have worked on analyzing the function of mast cells in cutaneous neurofibroma and aim to develop a new treatment method that suppresses the function of mast cells involved in tumor growth. There are still many gaps in knowledge regarding NF1. Neurofibroma tumors are known to contain a considerable number of mast cells though Professor Yamamoto found with the research has shown that each cell has an abnormally high concentration of an inflammatory substance called tryptase. This means that neurofibromas are constantly exposed to a strong inflammatory state, suggesting that it is difficult to stop tumor growth unless inflammation is stopped. Professor Yamamoto investigated the differences in the properties of disease-specific mast cells with NF1 gene mutations and mast cells derived from healthy subjects, and clarified differences in the production of tryptase, TGF-β1, and Stem Cell Factor. These findings suggest that tumor growth is driven by the overexpression of these proteins, and researchers believe that blocking the pathways that suppress the expression of these proteins can reduce inflammation and tumor growth.
通过抑制肥大细胞相关蛋白治疗神经纤维瘤肿瘤的新进展
1型神经纤维瘤病(NF1),也被称为von Recklinghausen病,是一种遗传性疾病,将来(很有可能)导致多发性良性肿瘤。NF1肿瘤有多种类型,除手术切除外,没有其他方法可以控制其发病率。副教授Misa Yamamoto是一位再生医学专家,目前正在进行一个项目,以阐明NF1患者的肿瘤生长机制。这将导致这种疾病的创新治疗方法的发展。研究人员隶属于日本山口大学医学研究生院临床检验科学系。目前,我们致力于分析肥大细胞在皮肤神经纤维瘤中的功能,旨在开发一种新的治疗方法,抑制肥大细胞参与肿瘤生长的功能。关于NF1的知识仍有许多空白。众所周知,神经纤维瘤肿瘤含有相当数量的肥大细胞,但山本教授在研究中发现,每个细胞都有一种异常高浓度的炎症物质,叫做胰蛋白酶。这意味着神经纤维瘤一直处于强烈的炎症状态,这表明除非停止炎症,否则很难阻止肿瘤的生长。Yamamoto教授研究了NF1基因突变的疾病特异性肥大细胞与来自健康受试者的肥大细胞特性的差异,并阐明了胰蛋白酶、TGF-β1和干细胞因子产生的差异。这些发现表明,肿瘤生长是由这些蛋白质的过度表达驱动的,研究人员认为,阻断抑制这些蛋白质表达的途径可以减少炎症和肿瘤生长。
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