Suppr超能文献

从 中分离得到的对胰腺癌有抗增殖和抗迁移作用的。

Antiproliferative and Antimigration Activities of Beauvericin Isolated from sp. on Pancreatic Cancer Cells.

机构信息

School of Pharmacy, Nihon University, 7-7-1 Narashinodai, Funabashi, Chiba 274-8555, Japan.

出版信息

Molecules. 2020 Oct 8;25(19):4586. doi: 10.3390/molecules25194586.

Abstract

This study describes the antiproliferative and antimigration effects of beauvericin from a culture broth of sp. in human pancreatic cancer cells (PANC-1). Activity-guided fractionation of the EtOAc extract of cultured broth of sp. RD055140 afforded beauvericin (), a new isariotin derivative, 7--methylisariotin C (), together with the known isariotin analogs, TK-57-164A () and B (). As a result of the measurement of the cell viability, inhibited cell growth (IC = 4.8 µM) of PANC-1 cells. Furthermore, was found to inhibit the migration activity of PANC-1 cells by upregulating the expression of the gene and reducing and genes in a dose-dependent manner (0.1-1 µM). These activities of had lower concentrations than the cytotoxic activity. These findings suggest that can be used as an anticancer agent against human pancreatic carcinoma.

摘要

本研究描述了从 sp. 的培养肉汤中分离出的 beauvericin 对人胰腺癌细胞(PANC-1)的抗增殖和抗迁移作用。对 sp. RD055140 培养肉汤的 EtOAc 提取物进行活性导向分离,得到 beauvericin (),一种新的 isariotin 衍生物,7--甲基异齿菌素 C (),以及已知的异齿菌素类似物,TK-57-164A () 和 B ()。由于细胞活力的测量,抑制了 PANC-1 细胞的生长(IC = 4.8 µM)。此外,发现通过上调基因的表达,并以剂量依赖的方式降低基因和基因(0.1-1 µM),抑制了 PANC-1 细胞的迁移活性。与细胞毒性活性相比,的这些活性具有更低的浓度。这些发现表明,可作为一种针对人类胰腺癌的抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1367/7582479/637f0863c009/molecules-25-04586-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验