Investigation of the inhibitory effects of simvastatin in RPMI 2650: An in-vitro study

Khafizatunnisa Jaapar, ZN Zuhairi, NA Sani Gapor, NA Bismelah, N. Mohamed
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Abstract

Objective: The present study was carried out to investigate the antiproliferative effects of simvastatin involving Human Squamous Nasal Cell Carcinoma (RPMI 2650 cell line), which is one of the most common head and neck cancers with the highest incidence and mortality rates in Asian countries. The anti-cancer effects of simvastatin in NPC have not yet been investigated in depth, hence it will be illustrated in the present study. Materials and methods: The cells were treated with various concentrations of Simvastatin in a dose dependent (0, 0.1, 0. 4, 3.0 mg/ml) and time dependent (24, 48 and 72 hours) manner. The cancer cell viability was then assessed by using MTT assay at absorbance of 590 nm. Results: Simvastatin induced reduction in cell viability number and induced apoptosis in RPMI 2650 cell line. Simvastatin for 72 h significantly reduced cell growth as compared to 48 and 24 h pre-incubation with simvastatin treatment. After 72 h incubation with 0.1 mg/ml, 0.4 mg/ml and 3.0 mg/ml simvastatin, the cell viability decreased from 100% in treated control cells to 23%, 21% and 14% respectively. Conclusions: This finding demonstrate the potential of simvastatin and probably may have therapeutic benefit for NPC cell growth.
辛伐他汀对RPMI 2650抑制作用的体外研究
目的:本研究旨在探讨辛伐他汀对亚洲国家发病率和死亡率最高的头颈部肿瘤之一——人鼻鳞癌(RPMI 2650细胞系)的抗增殖作用。辛伐他汀在鼻咽癌中的抗癌作用尚未深入研究,因此将在本研究中加以说明。材料和方法:不同浓度的辛伐他汀以剂量依赖性(0、0.1、0。4、3.0 mg/ml)和时间依赖性(24、48和72小时)。在590nm吸光度下,采用MTT法测定癌细胞活力。结果:辛伐他汀诱导RPMI 2650细胞株细胞活力降低,细胞凋亡。与辛伐他汀治疗前48和24小时相比,辛伐他汀治疗72小时显著降低细胞生长。0.1 mg/ml、0.4 mg/ml和3.0 mg/ml辛伐他汀孵育72 h后,对照细胞的细胞存活率分别从100%下降到23%、21%和14%。结论:这一发现证明了辛伐他汀的潜力,可能对鼻咽癌细胞生长有治疗益处。
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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