İlhan Özdemir, Fuat Zaman, Dilek Doğan Baş, Umut Sari, Şamil Öztürk, Mehmet Cudi Tuncer
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MTT analysis was performed, showing HeLa and HaCaT cell proliferation depending on the dose and duration of curcumin and doxorubicin. A wound scratch healing assay was applied to examine cell migration and invasion of HeLa after curcumin application. To determine the role of curcumin and doxorubicin in the apoptosis of HeLa cells, the mRNA levels of caspase-3 were examined by qRT-PCR. The results were analyzed with a one-way ANOVA SPSS 20.0 program.</p><p><strong>Results: </strong>CUR (IC50: 242.8 μM) and DOX (IC50: 92.1 μM) were determined to have the ability to inhibit the proliferation of HeLa cells and induce apoptosis over a 72-hour period and dose-dependently. Moreover, the results revealed that the mRNA and protein expression levels of RAF and RAS in HeLa cells were downregulated by CUR and DOX.</p><p><strong>Conclusions: </strong>The findings show that an alternative treatment method for cervical cancer can be developed with the application of CUR and DOX. 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引用次数: 0
摘要
目的:宫颈癌在女性不孕症中占有非常重要的地位,在女性癌症中排名第四。姜黄素(CUR)与各种调节蛋白的表达和活性密切相关。众所周知,姜黄素对各种癌症具有预防和治疗作用。方法:采用 qRT-PCR 和 Western 印迹分析评估姜黄素在 HeLa 和永生化人类皮肤角质细胞系(HaCaT)(RAS/RAF 信号通路的增殖和凋亡调节标志物)中的 mRNA 和蛋白质表达。MTT 分析显示,HeLa 和 HaCaT 细胞的增殖取决于姜黄素和多柔比星的剂量和持续时间。应用伤口划痕愈合试验来检测姜黄素应用后 HeLa 细胞的迁移和侵袭情况。为了确定姜黄素和多柔比星在 HeLa 细胞凋亡中的作用,采用 qRT-PCR 检测了 caspase-3 的 mRNA 水平。结果用 SPSS 20.0 程序进行单因素方差分析:结果表明,CUR(IC50:242.8 μM)和 DOX(IC50:92.1 μM)能够在 72 小时内抑制 HeLa 细胞的增殖并诱导细胞凋亡,且具有剂量依赖性。此外,研究结果表明,CUR和DOX能下调HeLa细胞中RAF和RAS的mRNA和蛋白表达水平:结论:研究结果表明,应用 CUR 和 DOX 可以开发出宫颈癌的替代治疗方法。结论:研究结果表明,应用 CUR 和 DOX 可以开发出宫颈癌的替代治疗方法。
Inhibitory effect of Curcumin on a cervical cancer cell line via the RAS/RAF signaling pathway.
Objective: Cervical cancer has a very important place in female infertility and ranks fourth among cancers affecting women. Curcumin (CUR) is closely associated with the expression and activity of various regulatory proteins. It is also known that curcumin has preventive and therapeutic effects on various types of cancer. In this study, the anticancer activities of curcumin were demonstrated in the human cervical cancer cell line (HeLa).
Methods: qRT-PCR and western blot analyses were used to evaluate mRNA and protein expression of curcumin in HeLa and immortalized human skin keratinocyte cell lines (HaCaT) (proliferation and apoptosis regulatory markers of the RAS/RAF signaling pathway). MTT analysis was performed, showing HeLa and HaCaT cell proliferation depending on the dose and duration of curcumin and doxorubicin. A wound scratch healing assay was applied to examine cell migration and invasion of HeLa after curcumin application. To determine the role of curcumin and doxorubicin in the apoptosis of HeLa cells, the mRNA levels of caspase-3 were examined by qRT-PCR. The results were analyzed with a one-way ANOVA SPSS 20.0 program.
Results: CUR (IC50: 242.8 μM) and DOX (IC50: 92.1 μM) were determined to have the ability to inhibit the proliferation of HeLa cells and induce apoptosis over a 72-hour period and dose-dependently. Moreover, the results revealed that the mRNA and protein expression levels of RAF and RAS in HeLa cells were downregulated by CUR and DOX.
Conclusions: The findings show that an alternative treatment method for cervical cancer can be developed with the application of CUR and DOX. Alternative methods for cervical cancer treatment may be developed using different methods in future studies.
期刊介绍:
HISTOLOGY AND HISTOPATHOLOGY is a peer-reviewed international journal, the purpose of which is to publish original and review articles in all fields of the microscopical morphology, cell biology and tissue engineering; high quality is the overall consideration. Its format is the standard international size of 21 x 27.7 cm. One volume is published every year (more than 1,300 pages, approximately 90 original works and 40 reviews). Each volume consists of 12 numbers published monthly online. The printed version of the journal includes 4 books every year; each of them compiles 3 numbers previously published online.