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肉桂酸衍生物可诱导癌细胞系的细胞周期停滞。

Cinnamic acid derivatives induce cell cycle arrest in carcinoma cell lines.

机构信息

University of Ljubljana, Faculty of Pharmacy, Askerceva 7, 1000 Ljubljana, Slovenia.

出版信息

Med Chem. 2013 Aug;9(5):633-41. doi: 10.2174/1573406411309050002.

Abstract

Cinnamic acid derivatives can be found in plant material, and they possess a remarkable variety of biological effects. In the present study, we have investigated the cytotoxic effects of representative cinnamic acid esters and amides. The cytotoxicity was determined by MTT test on human cervix adenocarcinoma (HeLa), myelogenous leukemia (K562), malignant melanoma (Fem-x), and estrogen-receptor-positive breast cancer (MCF-7) cells, versus peripheral blood mononuclear cells (PBMCs) without or with the addition of the plant lectin phytohemaglutinin (PHA). The compounds tested showed significant cytotoxicity (IC50s between 42 and 166 µM) and furthermore selectivity of these cytotoxic effects on the malignant cell lines versus the PBMCs was also seen, especially when electron-withdrawing groups, such as a cyano group (compound 5), were present on the aromatic rings of the alcohol or amine parts of the cinnamic acid derivatives. The additional study on cell cycle phase distribution indicated that novel cinnamic acid derivatives inhibit cell growth by induction of cell death. Thus, cinnamic acids derivatives represent important lead compounds for further development of antineoplastic agents.

摘要

肉桂酸衍生物存在于植物材料中,具有多种显著的生物效应。在本研究中,我们研究了代表性肉桂酸酯和酰胺的细胞毒性作用。通过 MTT 试验测定人宫颈腺癌(HeLa)、髓性白血病(K562)、恶性黑素瘤(Fem-x)和雌激素受体阳性乳腺癌(MCF-7)细胞以及外周血单个核细胞(PBMC)的细胞毒性,不添加或添加植物凝集素植物血球凝集素(PHA)。测试的化合物表现出显著的细胞毒性(IC50 在 42 到 166 µM 之间),并且这些细胞毒性作用对恶性细胞系与 PBMC 的选择性也可见,尤其是当吸电子基团,如氰基(化合物 5)存在于肉桂酸衍生物的醇或胺部分的芳环上时。对细胞周期相分布的进一步研究表明,新型肉桂酸衍生物通过诱导细胞死亡抑制细胞生长。因此,肉桂酸衍生物代表了进一步开发抗肿瘤药物的重要先导化合物。

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