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5-(双(3-(2-羟乙基)-1H-吲哚-2-基)甲基)-2-羟基苯甲酸(BHIMHA):展示了一种设计药物以阻断肿瘤肺转移的策略。

5-(Bis(3-(2-hydroxyethyl)-1H-indol-2-yl)methyl)-2-hydroxybenzoic acid (BHIMHA): showing a strategy of designing drug to block lung metastasis of tumors.

作者信息

Gan Taiping, Wang Yuji, Zhao Ming, Wu Jianhui, Yang Jian, Peng Shiqi

机构信息

Beijing Area Major Laboratory of Peptide and Small Molecular Drugs, Engineering Research Center of Endogenous Prophylactic of Ministry of Education of China; Beijing Laboratory of Biomedical Materials, College of Pharmaceutical Sciences, Capital Medical University, Beijing, People's Republic of China.

Beijing Area Major Laboratory of Peptide and Small Molecular Drugs, Engineering Research Center of Endogenous Prophylactic of Ministry of Education of China; Beijing Laboratory of Biomedical Materials, College of Pharmaceutical Sciences, Capital Medical University, Beijing, People's Republic of China; Department of Biomedical Science and Environmental Biology, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

Drug Des Devel Ther. 2016 Feb 16;10:711-21. doi: 10.2147/DDDT.S93570. eCollection 2016.

Abstract

Early metastasis is still the most recalcitrant factor in the treatment of lung cancer patients. By analyzing the structures and comparing the docking scores of the known pharmacophores, the authors of this paper designed 5-(bis(3-(2-hydroxyethyl)-1H-indol-2-yl)methyl)-2-hydroxybenzoic acid (BHIMHA) as a promising lead compound to develop metastasis inhibitors. In vitro 5, 10, and 20 µM of BHIMHA concentration dependently inhibited the migration and invasion of A549 cells. In vivo 0.4, 2.0, and 8.9 µmol/kg of BHIMHA dose dependently inhibited the metastasis of LLC (Lewis Lung Carcinoma) toward lung. In vivo, 2 µmol/kg of BHIMHA showed additional actions of slowing the growth of the primary tumor of C57BL/6 mice and S180 mice as well as inhibiting xylene-induced ear edema of the mice. Therefore, BHIMHA simultaneously blocked tumor metastasis toward lung, slowed the primary tumor growth, and limited the inflammation. These pharmacological actions were correlated with the inhibition of PKCα and NF-κB expression.

摘要

早期转移仍是肺癌患者治疗中最棘手的因素。通过分析已知药效团的结构并比较对接分数,本文作者设计了5-(双(3-(2-羟乙基)-1H-吲哚-2-基)甲基)-2-羟基苯甲酸(BHIMHA)作为开发转移抑制剂的一种有前景的先导化合物。体外实验中,5、10和20 μM的BHIMHA浓度依赖性地抑制A549细胞的迁移和侵袭。体内实验中,0.4、2.0和8.9 μmol/kg的BHIMHA剂量依赖性地抑制LLC(刘易斯肺癌)向肺部的转移。在体内,2 μmol/kg的BHIMHA还具有减缓C57BL/6小鼠和S180小鼠原发肿瘤生长以及抑制小鼠二甲苯诱导的耳部水肿的作用。因此,BHIMHA同时阻断肿瘤向肺部的转移、减缓原发肿瘤生长并限制炎症。这些药理作用与PKCα和NF-κB表达的抑制相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b391/4762582/390788a7d38c/dddt-10-711Fig1.jpg

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