Jiang Zhongyong, Liu Xi, Chang Kai, Liu Xia, Xiong Jie
Department of Clinical Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan, China (mainland).
Medical Department, Chengdu Military General Hospital, Chengdu, Sichuan, China (mainland).
Med Sci Monit. 2016 Nov 10;22:4283-4288. doi: 10.12659/MSM.897315.
BACKGROUND Because of the insensitivity of renal cell carcinoma (RCC) to both chemotherapy and radiotherapy, surgery remains the primary approach for anticancer treatment. However, patients who do not receive timely diagnoses may not be suitable for surgery, especially in the late phase of tumor development. Thus, the discovery of novel effective treatment is of great importance. Allyl isothiocyanate (AITC) can inhibit the proliferation and induce apoptosis in many cancer cells. In this paper, we report on an in vitro study to determine the effect of AITC on proliferation and apoptosis of RCC line GRC-1. MATERIAL AND METHODS CCK8 assay was used to detect cell proliferation under gradient concentrations of AITC. Flow cytometry was employed to evaluate cell apoptosis. Real-time fluorescent polymerase chain reaction quantified mRNA levels of Bax and Bcl-2 genes. Western blotting was further employed for protein expression assay. RESULTS AITC inhibited GRC-1 cell proliferation and induced cell apoptosis in a dose-dependent manner; it also elevated Bax while suppressing Bcl-2 gene expression at both mRNA and protein levels. In general, increasing concentration of AITC decreased Bcl-2/Bax ratio. CONCLUSIONS The inhibitory effect of AITC on GRC-1 cells is exerted via cell apoptosis, in which the imbalance of Bcl-2/Bax plays a significant role.
背景 由于肾细胞癌(RCC)对化疗和放疗均不敏感,手术仍然是抗癌治疗的主要方法。然而,未得到及时诊断的患者可能不适合手术,尤其是在肿瘤发展的晚期。因此,发现新的有效治疗方法至关重要。异硫氰酸烯丙酯(AITC)可抑制多种癌细胞的增殖并诱导其凋亡。在本文中,我们报告了一项体外研究,以确定AITC对肾癌细胞系GRC-1增殖和凋亡的影响。
材料与方法 采用CCK8法检测不同梯度浓度的AITC作用下的细胞增殖情况。运用流式细胞术评估细胞凋亡。实时荧光聚合酶链反应定量检测Bax和Bcl-2基因的mRNA水平。进一步采用蛋白质印迹法进行蛋白质表达检测。
结果 AITC以剂量依赖的方式抑制GRC-1细胞增殖并诱导细胞凋亡;在mRNA和蛋白质水平上,它还上调Bax表达,同时抑制Bcl-2基因表达。总体而言,AITC浓度增加会降低Bcl-2/Bax比值。
结论 AITC对GRC-1细胞的抑制作用是通过细胞凋亡实现的,其中Bcl-2/Bax的失衡起了重要作用。