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溴化偶氮脒:谜团、意外发现与前景。

Azoximer Bromide: Mystery, Serendipity, and Promise.

作者信息

Grivtsova Lyudmila Yuryevna, Falaleeva Natalia Alexandrovna, Tupitsyn Nikolay Nikolaevich

机构信息

A. Tsyb Medical Radiological Research Centre, National Medical Research Radiological Centre of Ministry of Health of the Russian Federation, Moscow, Russia.

Laboratory of Immunology of Hematopoiesis, N.N. Blokhin Cancer Research Center (RCRC), Moscow, Russia.

出版信息

Front Oncol. 2021 Sep 10;11:699546. doi: 10.3389/fonc.2021.699546. eCollection 2021.

Abstract

Azoximer bromide (AZB) was identified as an immunomodulator, and was initially developed and currently successfully indicated as one of several natural polyelectrolytes, a vaccine adjuvant, and an effective agent for the treatment of infectious and inflammatory diseases of viral, bacterial, and fungal origin. AZB has the potential to increase an individual's resistance to local and general infection and is indicated for the treatment of viral infections, and has also demonstrated clinical efficacy in the treatment of a variety of secondary immunodeficiencies. However, AZB may offer long-term promise beyond use against infection. Multiple clinical trials and research studies in cancer patients have reported favourable outcomes with AZB as well as an optimal safety and tolerability profile. The findings raise the possibility of direct antitumor properties. This literature review analyses the novel mechanisms that mediate the AZB direct anticancer effects. Overall, the evidence suggests that AZB has the hallmark of an agent that could be used to support existing cancer treatments at different stages of disease.

摘要

偶氮溴化物(AZB)被确定为一种免疫调节剂,最初作为几种天然聚电解质之一被开发,目前成功用作疫苗佐剂以及治疗病毒、细菌和真菌引起的感染性和炎症性疾病的有效药物。AZB有潜力增强个体对局部和全身感染的抵抗力,用于治疗病毒感染,并且在治疗多种继发性免疫缺陷方面也已显示出临床疗效。然而,AZB可能具有超越抗感染用途的长期前景。针对癌症患者进行的多项临床试验和研究报告称,AZB取得了良好的治疗效果,并且具有最佳的安全性和耐受性。这些发现增加了AZB具有直接抗肿瘤特性的可能性。这篇文献综述分析了介导AZB直接抗癌作用的新机制。总体而言,证据表明AZB具有可用于在疾病不同阶段支持现有癌症治疗药物的特征。

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Azoximer Bromide: Mystery, Serendipity, and Promise.溴化偶氮脒:谜团、意外发现与前景。
Front Oncol. 2021 Sep 10;11:699546. doi: 10.3389/fonc.2021.699546. eCollection 2021.

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