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砜衍生物作为抗炎和肿瘤细胞生长抑制剂的生物学评价

Biological evaluation of sulfone derivatives as anti-inflammatory and tumor cells growth inhibitory agents.

作者信息

Fang Shih-Hua, Padmavathi V, Rao Yerra Koteswara, Venkata Subbaiah D R C, Thriveni P, Geethangili Madamanchi, Padmaja A, Tzeng Yew-Min

机构信息

Department of Microbiology, School of Medicine, China Medical University, Taichung 404, Taiwan, ROC.

出版信息

Int Immunopharmacol. 2006 Nov;6(11):1699-705. doi: 10.1016/j.intimp.2006.07.004. Epub 2006 Jul 31.

DOI:10.1016/j.intimp.2006.07.004
PMID:16979124
Abstract

A variety of sulfone derivatives including three dimethyl arylsulfonyl malonates (1-3), two bis-(arylethenesulfonyl)-vinyl benzenes (4 and 5) and a sulfone triazole (6) were evaluated for their anti-inflammatory as well as tumor cells growth inhibitory activities in vitro. The sulfone derivatives 1, 2, 3 and 6 significantly and dose-dependently inhibited the production of inflammatory mediators such as nitric oxide (NO), and cytokines (tumor necrosis factor (TNF)-alpha and interleukin (IL)-12), in lipopolysaccharide (LPS) and interferon (IFN)-gamma activated murine peritoneal macrophages, without displaying cytotoxicity. The inhibitory mechanism is found through reducing iNOS protein expression. In addition, the derivatives 1-3 significantly arrest mitogen-stimulated spleen cells in G0/G1 stage, whereas compounds 4-6 blocked the same in the G2/M phase. Furthermore, the sulfone derivatives 3 and 6 showed dramatically reduction in the ratio of IFN-gamma to IL-4 production from mitogen-stimulated spleen cells. On the other hand, the novel compounds exhibited interesting cytotoxic activities against a panel of cell lines, particularly, 20 muM of compound 3 showed 50% cytotoxic effect on human hepatoma cell line, but has no effect on normal human peripheral blood mononuclear cells. In conclusion, compound 3 showed interesting anti-inflammatory and tumor cells growth inhibitory functions.

摘要

对多种砜衍生物进行了体外抗炎和肿瘤细胞生长抑制活性评估,这些衍生物包括三种二甲基芳基磺酰基丙二酸酯(1 - 3)、两种双(芳基乙烯基磺酰基)苯乙烯(4和5)以及一种砜基三唑(6)。砜衍生物1、2、3和6在脂多糖(LPS)和干扰素(IFN)-γ激活的小鼠腹腔巨噬细胞中,能显著且剂量依赖性地抑制一氧化氮(NO)等炎症介质以及细胞因子(肿瘤坏死因子(TNF)-α和白细胞介素(IL)-12)的产生,且无细胞毒性。发现其抑制机制是通过降低诱导型一氧化氮合酶(iNOS)蛋白表达。此外,衍生物1 - 3能显著使丝裂原刺激的脾细胞停滞在G0/G1期,而化合物4 - 6则在G2/M期阻断。此外,砜衍生物3和6使丝裂原刺激的脾细胞中IFN-γ与IL-4产生的比例显著降低。另一方面,这些新型化合物对一组细胞系表现出有趣的细胞毒性活性,特别是20 μM的化合物3对人肝癌细胞系显示出50%的细胞毒性作用,但对正常人外周血单个核细胞无影响。总之,化合物3表现出有趣的抗炎和肿瘤细胞生长抑制功能。

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