CA IX酶抑制对EZH2基因和组蛋白3修饰影响的研究

İbrahim Karakus, Özen Özensoy Guler
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RT-PCR was performed to determine the gene expression levels of Hypoxia-Inducible Factor 1A (HIF1A), Enhancer of Zeste Homolog 2 (EZH2) and CA IX. Results CA IX enzyme inhibition in the HT-29 cell line decreased the expression of CA IX (p<0.05) and HIF1A (p<0.01) genes and increased the expression of the EZH2 (p<0.05). There was a significant decrease in the expression of CA IX (p<0.05) and HIF1A genes as a result of inhibition with AZA performed under hypoxic conditions. It was observed that CA IX enzyme inhibition increases the expression of the EZH2 gene by more than 3 times (p<0.01). As a result of AZA inhibition, methylation levels were observed to increase in normoxic conditions, while methylation levels were observed to decrease in hypoxic conditions. 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引用次数: 0

摘要

摘要目的结肠癌是世界范围内最常见的胃肠道肿瘤,具有较高的发病率和死亡率。本研究的主要目的是阐明肿瘤相关碳酸酐酶IX (CA IX)酶抑制HT-29结肠癌细胞系CO 2 /HCO 3−缓冲系统中H +离子浓度效应对细胞表观遗传修饰的相互作用机制。方法采用人结肠癌细胞系HT-29进行细胞培养。给予caix酶抑制剂乙酰唑胺(AZA)。对细胞活力试验和抑制效果进行评价。进行细胞外pH测量。分离组蛋白总蛋白,ELISA法检测组蛋白H3修饰。RNA分离后,进行互补DNA合成。采用RT-PCR检测缺氧诱导因子1A (HIF1A)、Zeste同源物增强子2 (EZH2)和CA IX的基因表达水平。结果CA IX酶在HT-29细胞系中的抑制作用降低了CA IX (p<0.05)和HIF1A (p<0.01)基因的表达,增加了EZH2的表达(p<0.05)。缺氧条件下,由于AZA的抑制作用,CA IX和HIF1A基因的表达显著降低(p<0.05)。结果表明,CA IX酶抑制使EZH2基因表达量增加3倍以上(p<0.01)。由于AZA抑制,甲基化水平在常氧条件下升高,而在缺氧条件下甲基化水平降低。结论本研究通过观察H3修饰的变化以及CA IX、HIF1A和EZH2基因的表达变化,支持CA IX酶抑制在表观遗传修饰中发挥积极作用。
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Investigation of the effect of CA IX enzyme inhibition on the EZH2 gene and histone 3 modifications
Abstract Objectives Colon cancer is the most common gastrointestinal cancer worldwide with high morbidity and mortality rates. The main purpose of our study is to elucidate the interaction mechanism of the H + ion concentration effect in the CO 2 /HCO 3 − buffer system of tumor-associated Carbonic Anhydrase IX (CA IX) enzyme inhibition in the HT-29 colon cancer cell line on cell epigenetic modifications. Methods Cell culture was performed using the human colon cancer cell line HT-29. CA IX enzyme inhibitor Acetazolamide (AZA) was administered. The results of the cell viability test and inhibition were evaluated. Extracellular pH measurements were performed. Total histone protein isolation was performed and Histone H3 modifications were analyzed by ELISA method. After RNA isolation, complementary DNA (cDNA) synthesis was carried out. RT-PCR was performed to determine the gene expression levels of Hypoxia-Inducible Factor 1A (HIF1A), Enhancer of Zeste Homolog 2 (EZH2) and CA IX. Results CA IX enzyme inhibition in the HT-29 cell line decreased the expression of CA IX (p<0.05) and HIF1A (p<0.01) genes and increased the expression of the EZH2 (p<0.05). There was a significant decrease in the expression of CA IX (p<0.05) and HIF1A genes as a result of inhibition with AZA performed under hypoxic conditions. It was observed that CA IX enzyme inhibition increases the expression of the EZH2 gene by more than 3 times (p<0.01). As a result of AZA inhibition, methylation levels were observed to increase in normoxic conditions, while methylation levels were observed to decrease in hypoxic conditions. Conclusions Observing the changes in the H3 modifications and changes in the expression of CA IX, HIF1A and EZH2 genes in this study supports that CA IX enzyme inhibition plays an active role in epigenetic modifications.
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