Protocatechuic acid decreased telomerase reverse transcriptase (TERT) expression in DMBA-induced liver carcinogenesis mice model

S. El-Shaheed, H. Sahyon, M. Youssef, A. Negm
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引用次数: 3

Abstract

Background: The protocatechuic acid (PCA) is a natural polyphenolic antioxidant commonly distributed in plants and is considered as one of the main ingredients of some traditional herbal medicine. PCA has many pharmacological effects that may be closely linked to its antioxidant activity. Herein, we newly conducted this animal experiment to evaluate the therapeutic potentials of PCA on the 7,12-Dimethylbenzanthracene (DMBA) -induced hepatocarcinogenesis in the mouse model. Additionally, the in vitro antioxidant activity of PCA was estimated. Material and methods: To induce the hepatocarcinogenesis, DMBA (35 mg/kg, once per week) was orally administered for 4 weeks in the tumor test groups. After six weeks, the administration of PCA (100 mg/kg/day) was started for 4 weeks. Mice were sacrificed after ten weeks for measuring and comparing the serum hepatic enzymes level, antioxidant markers and telomerase reverse transcriptase (TERT) gene expression between the mice in DMBA with PCA (PCA group) and DMBA without PCA (non-PCA group). Also, the antioxidant activity of PCA was measured in vitro using two different antioxidant assays. Results: The elevation of all liver enzymes and other hepatic biomarkers observed in DMBA group were significantly suppressed in PCA-treated group. In addition, the TERT gene expression in liver tissue was significantly decreased in PCAtreated group. Our results also showed that the PCA exhibited a high antioxidant ability in vitro comparable to the positive control ascorbic acid. Conclusion: The protocatechuic acid decreased TERT expression and oxidative stress in DMBA-induced liver carcinogenesis mice model.
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原儿茶酸降低DMBA诱导肝癌小鼠模型中端粒酶逆转录酶(TERT)的表达
背景:原儿茶酸(procatechuic acid, PCA)是一种普遍存在于植物中的天然多酚类抗氧化剂,是一些传统草药的主要成分之一。PCA具有许多药理作用,可能与其抗氧化活性密切相关。在此,我们进行了新的动物实验,以评估PCA对7,12-二甲基苯并蒽(DMBA)诱导的小鼠肝癌模型的治疗潜力。此外,还对PCA的体外抗氧化活性进行了评价。材料与方法:肿瘤试验组口服DMBA (35 mg/kg,每周1次)诱导肝癌发生,连续4周。6周后,开始给予PCA (100 mg/kg/天)4周。10周后处死小鼠,测定并比较DMBA合并PCA组(PCA组)和DMBA不合并PCA组(非PCA组)小鼠血清肝酶水平、抗氧化标志物和端粒酶逆转录酶(TERT)基因表达。此外,采用两种不同的抗氧化测定法测定了PCA的体外抗氧化活性。结果:DMBA组肝酶及其他肝脏生物标志物的升高在pca处理组明显受到抑制。此外,治疗组肝组织中TERT基因表达明显降低。我们的研究结果还表明,PCA在体外表现出与阳性对照抗坏血酸相当的高抗氧化能力。结论:原儿茶酸可降低dba诱导肝癌小鼠模型中TERT的表达和氧化应激。
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来源期刊
Annals of Cancer Research and Therapy
Annals of Cancer Research and Therapy Medicine-Pharmacology (medical)
CiteScore
0.70
自引率
0.00%
发文量
18
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