苯甲酸对十种不同癌细胞株的细胞毒性作用

Hatice ÖZTÜRKEL KABAKAŞ, Merve Sezer Kürkçü, Kadriye Aslıhan ONAT TAŞDELEN, Bekir Çöl
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摘要

癌症种类繁多,是世界上最危险、最复杂的慢性疾病之一,影响着人类、社会和经济的福祉。在全球范围内,人们一直在探索和重新评估有效的化学物质、化合物和天然产品,将其作为减轻癌症及其相关症状的不良影响的潜在药物。在这一过程中,需要对潜在候选药物或治疗方案在体内外不同癌细胞类型上的细胞毒性活性进行初步评估。苯甲酸(BA)是一种芳香族羧酸,广泛存在于食品工业中,是可能具有相当抗癌潜力的酚酸之一。研究苯甲酸对不同癌症类型的比较效应是非常有用的。因此,在本研究中,我们使用 MTT 法检测了 BA 对十种不同癌症细胞系和一种正常细胞的细胞毒性,它们分别是前列腺癌(PC3)、宫颈癌(HeLA)、肝癌(HUH7)、结肠癌(CaCO2、HT29、SW48)、骨癌(MG63 和 A673)、咽癌(2A3)、肺癌(CRM612)和肾上皮对照细胞系(Phoenix)。结果发现,暴露于 BA 48 小时和 72 小时后的 IC50(µg/ml)值在 85.54±3.17 至 670.6±43.26 之间,而对照细胞株 Phoenix 的 IC 值分别为 410.54±32.29 和 231.16±25.25。考虑到 BA 对 11 种细胞类型的 IC50 值的统计评估,我们建议可以更详细地实施分子和组学方法,以找到 BA 的细胞和生化靶点,并阐明其分子作用模式,特别是从 MG63、CRM612 和 A673 癌细胞株开始,因为与对照细胞株相比,这些细胞株的 IC50 值相对最低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE CYTOTOXIC EFFECT OF BENZOIC ACID ON TEN DIFFERENT CANCER CELL LINES
Cancer, having numerous types, is among the most dangerous and complex chronic diseases in the world affecting the wellbeing of humans, society and economy. The exploration and reassessment of effective chemicals, compounds, and natural products as potential agents for alleviating the adverse effects of cancer and its related symptoms continue on a global scale. This process involves an initial evaluation of the cytotoxic activities of potential drug candidates or treatment regimens on diverse cancer cell types in an ex vivo context. Benzoic acid (BA), an aromatic carboxylic acid that is widely available and used in the food industry, is one of the phenolic acids that may bear considerable anti-cancer potential. It is useful to find out the comparable effect of BA on various cancer types. Therefore, in this study, we tested the cytotoxicity of BA using MTT assay, on a number of ten different cancer cell lines and one normal cell type, namely prostate cancer (PC3), cervical cancer (HeLA), liver cancer (HUH7), colon cancer (CaCO2, HT29, SW48), bone cancer (MG63 and A673), pharyngeal cancer (2A3), lung cancer (CRM612) and kidney epithelial control cell line (Phoenix), respectively. IC50 (µg/ml) values after 48 and 72-hour exposure to BA were found to differ between 85.54±3.17 to 670.6±43.26, while the IC values for the control cell line Phoenix were 410.54±32.29 and 231.16±25.25, respectively. Taking into account of statistical evaluation of the IC50 values for BA on 11 cell types, we suggest that the molecular and omics approaches can be implemented in more details in order to find cellular and biochemical targets of BA as well as elucidating molecular mode of action, especially starting with the cancer cell lines of MG63, CRM612 and A673, in which the IC50 levels are relatively the lowest compared to those of the control cell line.
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