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无花果果实乳汁对人癌细胞的细胞毒性。

Cytotoxicity of fig fruit latex against human cancer cells.

作者信息

Wang Jing, Wang Xiujie, Jiang Shu, Lin Ping, Zhang Jie, Lu Yanrong, Wang Qi, Xiong Zhujuan, Wu Yaying, Ren Jingjing, Yang Hongliang

机构信息

Division of Experimental Oncology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Sichuan Province, Chengdu, PR China.

出版信息

Food Chem Toxicol. 2008 Mar;46(3):1025-33. doi: 10.1016/j.fct.2007.10.042. Epub 2007 Nov 7.

Abstract

Fig fruit latex (FFL) contains significant amounts of polyphenolic compounds and can serve as a source of antioxidants after human consumption. The purpose of this study is to confirm anticancer activity of FFL against human cancer cells and to further elucidate its mechanism of activity. Human glioblastoma, hepatocellular carcinoma, and normal liver cells were used for in vitro tests of FFL effects. Those tests included cytotoxicity, colony formation inhibition, Brdu incorporation, acridine orange/ethidium bromide (AO/EB) staining for apoptotic cells, cell cycle distribution through flow cytometry (FCM), and ADP-ribosyltransferase (NAD+; poly(ADP-ribose) polymerase)-like 1 (ADPERL1) mRNA expression through RT-PCR in response to FFL treatment. After FFL treatment, the proliferation, colony formation, and Brdu labeling indices of cancer cells decreased (P<0.05), while the AO/EB stained apoptotic cells increased (P<0.05). By FCM analysis, an increase of G(0)/G(1) phase cell population and decrease of S and G(2)/M phase cells were observed (P<0.01), while both ADPRTL1 mRNA expression and apoptotic indices increased (P<0.01). The findings in these studies suggested that FFL exhibited potent cytotoxicity in some human cancer cells with little effect in normal cells at certain concentration. The mechanism for such effects might be associated with the inhibition of DNA synthesis, induction of apoptosis, and cell cycle arrest of cancer cells.

摘要

无花果果实乳胶(FFL)含有大量多酚类化合物,人类食用后可作为抗氧化剂的来源。本研究的目的是确认FFL对人类癌细胞的抗癌活性,并进一步阐明其作用机制。使用人胶质母细胞瘤、肝细胞癌和正常肝细胞进行FFL作用的体外试验。这些试验包括细胞毒性、集落形成抑制、溴脱氧尿苷掺入、吖啶橙/溴化乙锭(AO/EB)对凋亡细胞的染色、通过流式细胞术(FCM)分析细胞周期分布,以及通过逆转录聚合酶链反应(RT-PCR)检测ADP-核糖基转移酶(NAD+;聚(ADP-核糖)聚合酶)样1(ADPERL1)mRNA表达以响应FFL处理。FFL处理后,癌细胞的增殖、集落形成和溴脱氧尿苷标记指数降低(P<0.05),而AO/EB染色的凋亡细胞增加(P<0.05)。通过FCM分析,观察到G(0)/G(1)期细胞群体增加,S期和G(2)/M期细胞减少(P<0.01),而ADPRTL1 mRNA表达和凋亡指数均增加(P<0.01)。这些研究结果表明,FFL在某些人类癌细胞中表现出强大的细胞毒性,在一定浓度下对正常细胞影响很小。这种作用机制可能与抑制DNA合成、诱导凋亡和使癌细胞细胞周期停滞有关。

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