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大蕈氨酸,一种天然蕈菇三酸甘油脂,通过窖蛋白介导的对肌动蛋白细胞骨架的干扰,在体外和体内减少肿瘤生长。

Macrocybin, a Natural Mushroom Triglyceride, Reduces Tumor Growth In Vitro and In Vivo through Caveolin-Mediated Interference with the Actin Cytoskeleton.

机构信息

Oncology Area, Center for Biomedical Research of La Rioja (CIBIR), 26006 Logroño, Spain.

CsFlowchem, Campus Universidad San Pablo CEU, Boadilla del Monte, 28668 Madrid, Spain.

出版信息

Molecules. 2020 Dec 18;25(24):6010. doi: 10.3390/molecules25246010.

Abstract

Mushrooms have been used for millennia as cancer remedies. Our goal was to screen several mushroom species from the rainforests of Costa Rica, looking for new antitumor molecules. Mushroom extracts were screened using two human cell lines: A549 (lung adenocarcinoma) and NL20 (immortalized normal lung epithelium). Extracts able to kill tumor cells while preserving non-tumor cells were considered "anticancer". The mushroom with better properties was . Positive extracts were fractionated further and tested for biological activity on the cell lines. The chemical structure of the active compound was partially elucidated through nuclear magnetic resonance, mass spectrometry, and other ancillary techniques. Chemical analysis showed that the active molecule was a triglyceride containing oleic acid, palmitic acid, and a more complex fatty acid with two double bonds. The synthesis of all possible triglycerides and biological testing identified the natural compound, which was named Macrocybin. A xenograft study showed that Macrocybin significantly reduces A549 tumor growth. In addition, Macrocybin treatment resulted in the upregulation of Caveolin-1 expression and the disassembly of the actin cytoskeleton in tumor cells (but not in normal cells). In conclusion, we have shown that Macrocybin constitutes a new biologically active compound that may be taken into consideration for cancer treatment.

摘要

蘑菇被用作癌症治疗已有数千年的历史。我们的目标是从哥斯达黎加的热带雨林中筛选几种蘑菇物种,寻找新的抗肿瘤分子。使用两种人类细胞系(A549[肺腺癌细胞]和 NL20[永生化正常肺上皮细胞])筛选蘑菇提取物。能够杀死肿瘤细胞而保留非肿瘤细胞的提取物被认为是“抗癌”的。具有更好特性的蘑菇是. 具有积极特性的提取物进一步进行了分离,并在细胞系上测试了其生物活性。通过核磁共振、质谱和其他辅助技术部分阐明了活性化合物的化学结构。化学分析表明,活性分子是一种三酸甘油酯,含有油酸、棕榈酸和一种具有两个双键的更复杂脂肪酸。所有可能的三酸甘油酯的合成和生物测试确定了天然化合物,命名为 Macrocybin。异种移植研究表明,Macrocybin 可显著减少 A549 肿瘤的生长。此外,Macrocybin 处理导致肿瘤细胞中 Caveolin-1 表达上调和肌动蛋白细胞骨架解体(而在正常细胞中则没有)。总之,我们已经表明,Macrocybin 构成了一种新的具有生物活性的化合物,可能被考虑用于癌症治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/400e/7766322/b68ed24ab65c/molecules-25-06010-g001.jpg

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