HB-EGF特异性抑制剂-交叉反应物质197及其抗癌作用

M. Tanhapour, A. Golestani, A. Vaisi-Raygani, M. Aminian
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引用次数: 0

摘要

遗传异质性和转移仍然是癌症治疗中最具挑战性的方面。最近的研究介绍了白喉毒素的一种突变体,交叉反应物质197 (CRM197),作为一种新的有前景的生物抗癌药物,可以改善以前对化疗耐药的癌症治疗。crm197的弱毒性是其刺激细胞凋亡和抗肿瘤作用的主要原因。越来越多的证据表明,肝素结合的表皮生长因子样(HB-EGF)生长因子在大多数癌细胞中表达增加,而CRM197是其特异性抑制剂。本研究主要对CRM197的结构、性质和抗癌活性进行了研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cross-Reacting Material 197, a Specific Inhibitor of HB-EGF, and Its Anticancer Effects
Genetic heterogeneity and metastasis remain the most challenging aspects of cancer treatment.Recent studies have introduced a mutant of diphtheria toxin,cross-reacting material197 (CRM197), as a new promising biological anticancer drug to improve cancer therapy in patients previously resistant to chemotherapy. Weak toxicity of CRM197accounts forthe stimulation ofcell apoptosis and the antitumor effect. Increasing evidence has indicated that the expression of heparin-binding epidermal growth factor-like (HB-EGF) growth factorincreases in most cancer cells, and CRM197 is its specific inhibitor.This study has focused on the structure, properties, and anticancer activity of CRM197.
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