Hosseinpour Maryam, Mobini-Dehkordi Mohsen, Teimori Hossein
Faculty of Science, Department of Genetics, University of Shahrekord , Shahrekord, Iran .
Assistant Professor, Department of Genetics and Biotechnology, Cellular and Molecular Research Center, Shahrekord University of Medical Sciences , Shahrekord, Iran .
J Clin Diagn Res. 2016 Jul;10(7):FC05-8. doi: 10.7860/JCDR/2016/18149.8187. Epub 2016 Jul 1.
Over expression of squalene synthase gene causes induction of growth tumour and reduction of apoptosis. This gene which is conserved between Saccharomyces cerevisiae yeast and humans, is named (ERG9).
In this work, we studied the effect of Matricaria recutita extract on ERG9 gene (squalene synthase) expression in S.cerevisiae which was used as organism model in cancer therapy.
S. cerevisiae was cultured in YPD medium plus 0,250, 1000 and 3000 μg/ml of Matricaria recutita extract and we evaluated the (ERG9) gene expression by Real-time RT-PCR method after 24 hours.
At least 3 independent experiments were done. Data were analyzed using One-way ANOVA and Dunnett's test. A p-value of less than 0.01 was considered as significant.
We found that 250, 1000 and 3000 μg/ml of Matricaria recutita extract could reduce expression of ERG9 gene significantly (p<0.01). Interestingly, the expression of this gene was completely inhibited in 1000 and 3000 μg/ml concentrations.
This study predicted that Matricaria recutita extract produced anti-cancer effects in humans, because it could inhibit the expression of an analogue key gene in this malignant disease. Further investigations should be made, to study its molecular mechanism of action at the mammal cell level.
角鲨烯合酶基因的过度表达会导致肿瘤生长诱导和细胞凋亡减少。该基因在酿酒酵母和人类之间保守,被命名为(ERG9)。
在本研究中,我们研究了洋甘菊提取物对酿酒酵母中ERG9基因(角鲨烯合酶)表达的影响,酿酒酵母被用作癌症治疗的生物模型。
将酿酒酵母在含有0、250、1000和3000μg/ml洋甘菊提取物的YPD培养基中培养,24小时后通过实时RT-PCR方法评估(ERG9)基因表达。
至少进行3次独立实验。数据采用单因素方差分析和Dunnett检验进行分析。p值小于0.01被认为具有显著性。
我们发现250、1000和3000μg/ml的洋甘菊提取物可显著降低ERG9基因的表达(p<0.01)。有趣的是,在1000和3000μg/ml浓度下该基因的表达被完全抑制。
本研究预测洋甘菊提取物对人类具有抗癌作用,因为它可以抑制这种恶性疾病中类似关键基因的表达。应进一步开展研究,以在哺乳动物细胞水平上研究其作用的分子机制。