Comparison of the Therapeutic Effect of Sinapic Acid in Drug-Resistant and Non-Resistant Hepatocellular Carcinoma Cells

Fatma Secer Celik, Canan Eroglu Gunes, E. Kurar
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Abstract

Sinapic acid (SA) has been shown to have anti-bacterial, anti-cancer, anti-inflammatory, cardioprotective, hepatoprotective, and neuroprotective effects in pre-clinical and in vitro investigations. Especially in cancer studies, it has been shown that SA has an anti-cancer effect. SA reduced proliferation and induced apoptosis in cancer cells. In this study, the effect of SA on drug resistance in hepatocellular carcinoma was investigated. For this purpose, cells resistant to sorafenib were obtained. According to the gene expression analysis performed in resistant cells, the expression of MDR1, hCE-1 and hCE-2 increased significantly. Then, specific doses of sinapic acid were applied to both Hep3B and resistant Hep3B cell lines. The IC50 dose for Hep3B cells was determined by XTT analysis. The cytotoxic effect of SA was different in resistant and non-resistant cells. The IC50 dose of SA was increased in resistant cells compared to Hep3B cells. The chemotherapeutic applications of herbal chemicals have been widely studied. However, drug resistance against frequently used chemotherapeutics is the biggest obstacle to treatment. This study showed that the dose of SA applied to resistant cells should be increased. This suggests that when the resistance mechanism occurs, the herbal chemicals are also effused out of the cell like drugs. It is necessary to study the intracellular interactions of SA with further studies.
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比较西那皮酸对耐药和非耐药肝细胞癌细胞的治疗效果
在临床前和体外研究中,西那皮酸(SA)已被证明具有抗菌、抗癌、消炎、保护心脏、保护肝脏和保护神经的作用。特别是在癌症研究中,研究表明南澳大利亚具有抗癌作用。南澳大利亚能减少癌细胞的增殖并诱导其凋亡。本研究调查了 SA 对肝细胞癌耐药性的影响。为此,研究人员获得了对索拉非尼耐药的细胞。根据耐药细胞的基因表达分析,MDR1、hCE-1 和 hCE-2 的表达明显增加。然后,将特定剂量的西那非酸应用于 Hep3B 和耐药 Hep3B 细胞系。通过 XTT 分析确定了 Hep3B 细胞的 IC50 剂量。在耐药和非耐药细胞中,SA 的细胞毒性作用是不同的。与 Hep3B 细胞相比,SA 在耐药细胞中的 IC50 剂量有所增加。中草药化学物质的化疗应用已被广泛研究。然而,对常用化疗药物的耐药性是治疗的最大障碍。这项研究表明,对耐药细胞使用的 SA 剂量应该增加。这表明,当出现耐药机制时,中草药化学物质也会像药物一样从细胞中流出。有必要进一步研究 SA 在细胞内的相互作用。
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