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藏红花素抑制人舌鳞状细胞癌细胞系Tca8113的增殖和核酸合成并诱导其凋亡。

Crocin inhibits proliferation and nucleic acid synthesis and induces apoptosis in the human tongue squamous cell carcinoma cell line Tca8113.

作者信息

Sun Jun, Xu Xiao-meng, Ni Chen-zhong, Zhang Hong, Li Xiao-yu, Zhang Chao-liang, Liu Yu-rong, Li Sheng-fu, Zhou Qi-zhi, Zhou Hong-mei

机构信息

State Key Laboratory of Oral Diseases, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Asian Pac J Cancer Prev. 2011;12(10):2679-83.

Abstract

BACKGROUND

Cancer chemoprevention is a proven effective strategy for oral squamous cell carcinoma (OSCC). The present study was designed to investigate the effects of crocin, a potential chemopreventive agent, on growth and DNA and RNA content in a human tongue squamous cell carcinoma cell line, Tca8113.

METHODS

Tca8113 cells were treated with crocin for 24, 48, 72, and 96 h at concentrations of 0.1, 0.2, 0.4, and 0.8 mM. Tumor cell viability was investigated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay. In addition, Tca8113 cells were treated with 0.4 mM crocin and cytotoxic effects as an inducer of apoptosis were analyzed using flow cytometry. Furthermore, acridine orange (AO) staining and observation using laser scanning confocal microscopy (LSCM) were used to determine the effects of the drug on nucleic acid synthesis.

RESULTS

Crocin decreased Tca8113 cell viability and growth remarkably at 24, 48, 72, and 96 h, in a concentration-dependent manner (P<0.05). In addition, 0.4 mM crocin significantly induced both early and late apoptosis of Tca8113 cells. Moreover, the cellular DNA and RNA content was significantly downregulated by 0.4 mM crocin compared with the negative control (P<0.01).

CONCLUSIONS

Our observations support the feasibility of applying crocin as a chemoprophylactic agent and treatment for OSCCs.

摘要

背景

癌症化学预防是一种已被证实对口腔鳞状细胞癌(OSCC)有效的策略。本研究旨在调查藏红花素(一种潜在的化学预防剂)对人舌鳞状细胞癌细胞系Tca8113的生长以及DNA和RNA含量的影响。

方法

用浓度为0.1、0.2、0.4和0.8 mM的藏红花素处理Tca8113细胞24、48、72和96小时。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)法研究肿瘤细胞活力。此外,用0.4 mM藏红花素处理Tca8113细胞,并使用流式细胞术分析作为凋亡诱导剂的细胞毒性作用。此外,使用吖啶橙(AO)染色并通过激光扫描共聚焦显微镜(LSCM)观察来确定该药物对核酸合成的影响。

结果

藏红花素在24、48、72和96小时时显著降低Tca8113细胞活力和生长,呈浓度依赖性(P<0.05)。此外,0.4 mM藏红花素显著诱导Tca8113细胞的早期和晚期凋亡。而且,与阴性对照相比,0.4 mM藏红花素显著下调细胞DNA和RNA含量(P<0.01)。

结论

我们的观察结果支持将藏红花素用作OSCC化学预防剂和治疗药物的可行性。

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