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首页> 外文期刊>Pathology oncology research: POR >Tumor Preventive Efficacy of Emodin in 7,12-Dimethylbenz[a]Anthracene-Induced Oral Carcinogenesis: a Histopathological and Biochemical Approach
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Tumor Preventive Efficacy of Emodin in 7,12-Dimethylbenz[a]Anthracene-Induced Oral Carcinogenesis: a Histopathological and Biochemical Approach

机译:大黄素肿瘤预防疗效在7,12-二甲基苯并[A]蒽酰诱导的口腔致癌作用中:组织病理学和生化方法

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摘要

Abstract The aim of the present study is to focus the chemopreventive potential of Emodin during 7,12-dimethylbenz[a]anthracene (DMBA) induced hamster buccal pouch carcinogenesis. Tumors were developed in the buccal pouches of golden Syrian hamsters by painting with 0.5% DMBA thrice a week for 14?weeks. The status of lipid peroxidation, antioxidants and detoxification agents were utilized as biochemical endpoints and the expression pattern of apoptotic proteins was employed as molecular endpoints in addition to the histopathological studies, to substantiate the anticancer potential of Emodin. Hamsters treated with DMBA + Emodin revealed mild to moderate precancerous lesions such as hyperplasia and dysplasia whereas 100% tumor formation was noticed in hamsters treated with DMBA alone. Also, Emodin treatment modulated the status of lipid peroxidation, antioxidants, phase I and II detoxification agents and apoptotic proteins in favor of the inhibition/reversal/suppression of the oral tumorigenesis in DMBA treated hamsters. The present study thus concludes that the chemopreventive potential of Emodin relies on its pro-apoptotic and antioxidant efficacy during DMBA induced hamster buccal pouch carcinogenesis.
机译:摘要本研究的目的是将大黄素的化学预防潜力聚焦在7,12-二甲基苯并[a]蒽(DMBA)诱导的仓鼠颊癌癌发生中。通过每周用0.5%的DMBA绘画,在金叙利亚仓鼠的口腔袋中开发了肿瘤,每周涂上0.5%的DMBA 14个星期。利用脂质过氧化,抗氧化剂和排毒剂的状态作为生化终点,除了组织病理学研究之外,凋亡蛋白的表达模式还用作分子终点,以证实大黄素的抗癌潜力。用DMBA + Emodin治疗的仓鼠显示出轻度至中度前癌变病变,如增生和发育不良,而100%肿瘤形成在用DMBA处理的仓鼠中被注意到。此外,大黄素治疗调节脂质过氧化,抗氧化剂,II和II解毒剂和凋亡蛋白的状态,有利于DMBA处理的仓鼠中口腔肿瘤的抑制/逆转/抑制。因此,本研究得出结论,大黄素的化学预防潜力依赖于DMBA诱导仓鼠颊囊癌发生中的促凋亡和抗氧化效果。

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