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NF-κB/PI3K/AKT信号通路在鼠李素对二乙基亚硝胺诱导的大鼠肝细胞癌发生的保护作用中的参与情况。

Involvement of NF-κB/PI3K/AKT signaling pathway in the protective effect of prunetin against a diethylnitrosamine induced hepatocellular carcinogenesis in rats.

作者信息

Li Guanghua, Qi Li, Chen Hui, Tian Gendong

机构信息

Department of Gastrointestinal Surgery, The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.

Department of Gastroenterology, Binzhou People's Hospital, Binzhou, China.

出版信息

J Biochem Mol Toxicol. 2022 May;36(5):e23016. doi: 10.1002/jbt.23016. Epub 2022 Mar 3.

Abstract

Prunetin (PRU) is an O-methylated flavonoid that is present in various natural plants and a primary significant compound found in isoflavone. Liver cancer creates major carcinogenic death despite recently advanced therapies. Hepatocellular carcinoma (HCC) treatment and prognosis are better in people with secure liver function. In the present study, we evaluated the action of PRU on diethylnitrosamine (DEN) alone HCC in a rat model through inflammation-mediated cell proliferative phosphoinositide 3-kinase/protein kinase B (PI3K/AKT) pathway analysis. Male Wistar rats were divided into four groups of six rats each. Group I, normal rats; Group II, DEN alone; Group III, DEN + PRU, and Group IV, PRU-alone. All groups of rats carried out hepatic cancer development by hypothesis antioxidant, biochemical, cell proliferative, apoptosis, cytokines protein, and gene expression status profiles. In tumor incidence DEN + PRU, 100% delayed the tumor growth disappearance of the lesion,  and reversal of normal liver architecture was observed. Liver marker enzymes levels decreased when antioxidant levels (superoxidase dismutase, catalase, glutathione peroxidase, and glutathione reductase) were in Group III. Proinflammatory markers nuclear factor-κB, interleukin (IL)-6, IL-1β, and tumor necrosis factor α, were elevated in the rat's serum in Group III. Cell proliferative markers proliferating cell nuclear antigen and Cyclin-D1 protein expressions were downregulated; in contrast, Bcl-2, Bax, caspase-3, and caspase-9 gene expressions were upregulated and then it followed that protein expression of PI3K/AKT was downregulated in PRU-treated groups. PRU assisted reversal of liver damage, antioxidant enzyme restoration cytokine balance, protein, and gene expression to control levels. Taken together, PRU improves functions of the liver, and as such prevents HCC. PRU can be used together with chemopreventives for HCC.

摘要

樱黄素(PRU)是一种存在于多种天然植物中的O - 甲基化黄酮类化合物,也是异黄酮中发现的一种主要重要化合物。尽管最近有先进的治疗方法,但肝癌仍是主要的致癌死亡原因。肝功能正常的人肝细胞癌(HCC)的治疗效果和预后较好。在本研究中,我们通过炎症介导的细胞增殖磷酸肌醇3激酶/蛋白激酶B(PI3K/AKT)通路分析,评估了PRU对大鼠模型中单独由二乙基亚硝胺(DEN)诱导的肝癌的作用。雄性Wistar大鼠被分为四组,每组六只。第一组,正常大鼠;第二组,单独使用DEN;第三组,DEN + PRU;第四组,单独使用PRU。通过假设的抗氧化、生化、细胞增殖、凋亡、细胞因子蛋白和基因表达状态谱,对所有组的大鼠进行肝癌发生情况研究。在肿瘤发生率方面,DEN + PRU组100%延迟了肿瘤生长,病变消失,且观察到正常肝脏结构的逆转。当第三组的抗氧化水平(超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶和谷胱甘肽还原酶)升高时,肝脏标志物酶水平下降。第三组大鼠血清中的促炎标志物核因子 - κB、白细胞介素(IL)-6、IL -1β和肿瘤坏死因子α升高。细胞增殖标志物增殖细胞核抗原和细胞周期蛋白D1蛋白表达下调;相反,PRU处理组中Bcl -2、Bax、半胱天冬酶 -3和半胱天冬酶 -9基因表达上调,随后PI3K/AKT的蛋白表达下调。PRU有助于肝脏损伤的逆转、抗氧化酶恢复、细胞因子平衡以及蛋白质和基因表达恢复到对照水平。综上所述,PRU改善肝脏功能,从而预防HCC。PRU可与HCC的化学预防剂联合使用。

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