Some pleiotropic effects of statins on hepatocellular carcinoma cells: Comparative study on atorvastatin, rosuvastatin and simvastatin

IF 2.5 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Esmeralda Dautović , Monika Rustemović-Čorbić , Nahida Srabović , Adaleta Softić , Aida Smajlović , Maida Šljivić Husejnović , Alen Hatkić , Dalila Halilčević
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引用次数: 0

Abstract

Purpose

For many years, statins have been the most commonly used drugs in cholesterol-lowering therapy. In addition to these therapeutic effects, statins exhibit other, pleiotropic effects that can be beneficial, but also harmful to cells and tissues. The aim of this research was to determine and compare the pleiotropic effects of structurally different statins: atorvastatin, simvastatin and rosuvastatin at different concentrations on hepatocellular carcinoma (HepG2) cells.

Materials and methods

The MTT assay was used to determine the cytotoxic effects of statins. The influence of statins on the production of reactive oxygen species (ROS) was determined by measuring fluorescent response of 2,7-dichlorofluorescein diacetate (DCFH-DA). The effect of statins on glucose production and excretion was determined with glucose production assay.

Results

The obtained results confirmed that all tested statins exhibit cytotoxic effects, increase the production of ROS as well as the production and excretion of glucose from HepG2 cells. It was observed that all the mentioned effects are more pronounced with lipophilic statins, atorvastatin and simvastatin compared to hydrophilic rosuvastatin.

Conclusion

The less pronounced pleiotropic effects of rosuvastatin on HepG2 cells are probably due to differences in structure and solubility compared to atorvastatin and simvastatin. Transporter-dependent and a slower influx of rosuvastatin into cells compared to the tested lipophilic statins probably lead to a weaker accumulation of rosuvastatin in HepG2 cells, which results in less pronounced pleiotropic effects compared to lipophilic atorvastatin and simvastatin.

他汀类药物对肝癌细胞的多效作用:阿托伐他汀、瑞舒伐他汀和辛伐他汀的比较研究
目的多年来,他汀类药物一直是降胆固醇治疗中最常用的药物。除了这些治疗作用外,他汀类药物还表现出其他多效性作用,这些作用可能有益,但也对细胞和组织有害。本研究的目的是确定和比较结构不同的他汀类药物:不同浓度的阿托伐他汀、辛伐他汀和瑞舒伐他汀对肝细胞癌(HepG2)细胞的多效性作用。材料与方法MTT法测定他汀类药物的细胞毒作用。通过测定2,7-二氯荧光素二乙酸酯(DCFH-DA)的荧光响应,测定了他汀类药物对活性氧(ROS)产生的影响。用葡萄糖生成测定法测定他汀类药物对葡萄糖生成和排泄的影响。结果所有测试的他汀类药物都表现出细胞毒性作用,增加了HepG2细胞ROS的产生以及葡萄糖的产生和排泄。观察到,与亲水性瑞舒伐他汀相比,亲脂性他汀类药物、阿托伐他汀和辛伐他汀的所有上述效果都更显著。结论瑞舒伐他汀对HepG2细胞的多效性作用不太明显,可能是由于与阿托伐他汀和辛伐他汀相比,其结构和溶解度存在差异。与测试的亲脂性他汀类药物相比,转运蛋白依赖性和瑞舒伐他汀流入细胞的速度较慢可能导致瑞舒伐丁在HepG2细胞中的积聚较弱,这导致与亲脂性阿托伐他汀和辛伐他汀相比,多效性作用不太明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in medical sciences
Advances in medical sciences 医学-医学:研究与实验
CiteScore
5.00
自引率
0.00%
发文量
53
审稿时长
25 days
期刊介绍: Advances in Medical Sciences is an international, peer-reviewed journal that welcomes original research articles and reviews on current advances in life sciences, preclinical and clinical medicine, and related disciplines. The Journal’s primary aim is to make every effort to contribute to progress in medical sciences. The strive is to bridge laboratory and clinical settings with cutting edge research findings and new developments. Advances in Medical Sciences publishes articles which bring novel insights into diagnostic and molecular imaging, offering essential prior knowledge for diagnosis and treatment indispensable in all areas of medical sciences. It also publishes articles on pathological sciences giving foundation knowledge on the overall study of human diseases. Through its publications Advances in Medical Sciences also stresses the importance of pharmaceutical sciences as a rapidly and ever expanding area of research on drug design, development, action and evaluation contributing significantly to a variety of scientific disciplines. The journal welcomes submissions from the following disciplines: General and internal medicine, Cancer research, Genetics, Endocrinology, Gastroenterology, Cardiology and Cardiovascular Medicine, Immunology and Allergy, Pathology and Forensic Medicine, Cell and molecular Biology, Haematology, Biochemistry, Clinical and Experimental Pathology.
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