The antiproliferative and cytotoxic effects of curcumin on human cervical cancer Hep2C cell line

F. Alanyalı, M. Alkan
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Abstract

Objective: In this study, antiproliferative and cytotoxic effects of different concentrations of curcumin on cervical cancer Hep2C cells were investigated with microscopic methods and MTT assay. Methods: Hep2C (human carcinoma cancer cell line, ATCC:CCL-23) cells were cultured. For cytotoxicity evaluation Hep2C cells exposed to curcumin at different concentrations of 30 µg/ml, 15 µg/ml, 7.5 µg/ml, 3.7 µg/ml, 1.9 µg/ml, 0.9 µg/ml, 0.45 µg/ml for 24 hours These Hep2C cells are evaluated with MTT assay. The IC 50 value of the agent for 24 h of exposure was detected. The graph of the absorbance data obtained by the Spectramax I3 device. Viability values of Hep2C cells calculated from the absorbances obtained from MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay are gained. The preparations were observed based on changes in nuclei and structures using an inverted microscope (Leica Microsystems). Nontreated cells were used as negative control and for positive control Hep2C cells were exposed to ammonium molibdate (1mg/ml) for the above given incubation period. hücre kültürü Results: High doses of curcumin µg/ml, 15 µg/ml, 7.5 µg/ml) showed high antiproliferative and cytotoxic effects on Hep2C cells. The antiproliferative and cytotoxic effects were not observed on cervical cancer Hep2C cells treated with lower concentrations of curcumin. Conclusion: Curcumin has been shown that it is non-toxic, can be used as a highly antioxidant and anti-inflammatory agent and has multifaced therapeutic-pharmacological effects. However, researches on the antiproliferative, anti-cancer effects of curcumin in cervical cancer cells is not sufficient. The present study evaluates the antiproliferative and cytotoxic effects of curcumin on human cervical cancer Hep2C cells as the first time. The results of our study support these effects of curcumin on Hep2C cells in a concentration-dependent
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姜黄素对人宫颈癌Hep2C细胞系的抗增殖和细胞毒作用
目的:采用显微法和MTT法研究不同浓度姜黄素对宫颈癌Hep2C细胞的抗增殖和细胞毒作用。方法:培养Hep2C(人癌细胞系,ATCC:CCL-23)细胞。Hep2C细胞暴露于不同浓度姜黄素(30µg/ml、15µg/ml、7.5µg/ml、3.7µg/ml、1.9µg/ml、0.9µg/ml、0.45µg/ml) 24h后,采用MTT法评价Hep2C细胞的细胞毒性。检测暴露24 h后的ic50值。Spectramax I3设备获得的吸光度数据曲线图。根据MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑)测定获得的吸光度计算Hep2C细胞的活力值。利用倒置显微镜(Leica Microsystems)观察制备过程中细胞核和结构的变化。将未处理的细胞作为阴性对照,将Hep2C细胞暴露于molib酸铵(1mg/ml)中进行上述给定的孵育期,作为阳性对照。h cre kültürü结果:高剂量姜黄素(µg/ml、15µg/ml、7.5µg/ml)对Hep2C细胞具有较高的抗增殖和细胞毒作用。低浓度姜黄素对宫颈癌Hep2C细胞的抗增殖和细胞毒作用未观察到。结论:姜黄素无毒,可作为一种高抗氧化和抗炎剂,具有多方面的治疗药理作用。然而,姜黄素对宫颈癌细胞的抗增殖、抗癌作用的研究尚不充分。本研究首次评价了姜黄素对人宫颈癌Hep2C细胞的抗增殖和细胞毒作用。我们的研究结果支持姜黄素对Hep2C细胞的影响呈浓度依赖性
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