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苦木苦味素的临床前和临床活性:一种有潜力的抗癌药物。

The preclinical and clinical activity of aviscumine: a potential anticancer drug.

机构信息

Universitätsklinik Innsbruck, Department of Internal Medicine, Anichstrasse 35, A-6020 Innsbruck, Austria.

出版信息

Eur J Cancer. 2011 Jul;47(10):1450-7. doi: 10.1016/j.ejca.2011.02.022. Epub 2011 Apr 12.

Abstract

Extracts from the European mistletoe plant Viscumalbum have been studied for decades for their direct and indirect anticancer activity. Therefore, scientists were interested in identifying the active compound (mistletoe lectin) in these extracts and making it available as a highly purified molecule for drug development. Recombinant mistletoe lectin (INN: aviscumine) was produced in Escherichiacoli. It has been shown to have immunomodulatory and cytotoxic activity in invitro and in animal models and can target tumour cells. Clinical phase I studies also demonstrated immunomodulatory activity, which appears to have a positive effect on disease stabilisation. This review explores the current knowledge base for aviscumine's mechanism of action, efficacy and side-effects in both preclinical studies and clinical trials, and it considers aviscumine's potential as a cancer therapy.

摘要

欧洲槲寄生植物的提取物已被研究了几十年,因其具有直接和间接的抗癌活性。因此,科学家们有兴趣鉴定这些提取物中的活性化合物(槲寄生凝集素),并将其作为一种高度纯化的分子用于药物开发。重组槲寄生凝集素(INN:aviscumine)在大肠杆菌中产生。它已被证明在体外和动物模型中具有免疫调节和细胞毒性活性,并且可以靶向肿瘤细胞。临床 I 期研究也表明具有免疫调节活性,这似乎对疾病稳定有积极影响。这篇综述探讨了 aviscumine 在临床前研究和临床试验中的作用机制、疗效和副作用的现有知识库,并考虑了它作为癌症治疗的潜力。

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