摘要
细胞外信号/β-连环信号通路的异常活化通常与癌症的发展相关。然而,控制的细胞外 /β-连环信号通路仅阐明了部分的分子机制。在这里,我们表明,β连环蛋白是不同调制的患者多发性硬化(MS),其中显示用于临床的MS管理不同药物治疗引起β连环蛋白的不同核表达水平。蛋白质由外周血单核细胞中提取进行了评估,以评估β连环蛋白的免疫印迹的表达水平。分析我们的结果,我们意识到,β-连环蛋白完全是由那他珠单抗抑制,可能在MS的管理起作用。这可能会提供新的有前途的研究主要集中在β-连环蛋白的易位的可能性治疗控制。
关键词: 复发/多发性硬化缓解,第一个患者诊断,细胞外 /β-连环信号通路,那他珠单抗,β-干扰素
Current Molecular Medicine
Title:Is β-catenin neutralization cross-involved in the mechanisms mediated by natalizumab action?
Volume: 15 Issue: 10
Author(s): M. Galuppo, E. Mazzon, S. Giacoppo, O. Bereshchenko, S. Bruscoli, C. Riccardi and P. Bramanti
Affiliation:
关键词: 复发/多发性硬化缓解,第一个患者诊断,细胞外 /β-连环信号通路,那他珠单抗,β-干扰素
摘要: Aberrant activation of Wnt/β-catenin signaling pathway is commonly associated to cancer development. However, molecular mechanisms controlling Wnt/β-catenin signaling pathway have been clarified only in part. Here, we show that β-catenin is differently modulated in patients with multiple sclerosis (MS), displaying that different pharmacological treatments used for clinical MS management cause different nuclear expression levels of β-catenin. Proteins extracted by peripheral blood mononuclear cells were assessed to evaluate the western blot expression levels of β-catenin. Analyzing our results, we realized that β-catenin is totally inhibited by Natalizumab and could have a role in MS management. This could offer new promising studies focused on the possible therapeutic control of β-catenin translocation.
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Cite this article as:
M. Galuppo, E. Mazzon, S. Giacoppo, O. Bereshchenko, S. Bruscoli, C. Riccardi and P. Bramanti , Is β-catenin neutralization cross-involved in the mechanisms mediated by natalizumab action?, Current Molecular Medicine 2015; 15 (10) . https://dx.doi.org/10.2174/1566524016666151123114825
DOI https://dx.doi.org/10.2174/1566524016666151123114825 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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