Chemopreventive potential of goniothalamin in diethylnitrosamine-induced hepatocellular carcinoma through the suppression of P13K/AKT signalling pathway.

IF 1.6 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Jie Li, Dong Zhan, Cui Chen, Rongfu Li, Fang-Qing Zhu
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Abstract

Liver cancer is the most lethal form of cancer and carries a high risk of death around the world. Goniothalamin (GTN) is a styryl-lactone that possesses antiproliferative and apoptotic activity. The molecular action of GTN is not yet fully evaluated. Thus, our research has been intended to assess the chemopreventive and apoptotic activities of diethylnitrosamine (DEN)-induced hepatocellular carcinoma (HCC) in rats. Rats were separated into 4 groups: control, DEN only, DEN + GTN (30 mg/kg bw), and GTN (30 mg/kg bw) alone. We evaluated body weight, liver weight, tumor incidence, hepatic toxic markers, antioxidants, inflammatory cytokines, histopathology, immunohistochemistry, and Western blot studies. DEN lessened body weight, antioxidants, and apoptosis, whereas it elevated tumor incidence, toxic markers, cytokines, and Bcl-2 expression. GTN treatment maintains body weight, liver weight, and antioxidant levels, and it also prevents tumor incidence, oxidative stress, toxic markers, pro-inflammatory cytokines, and histological changes. It triggers apoptosis by constraining Bcl-2 and elevating caspase-3 levels. GTN also attenuated the P13K/ AKT signaling which enhanced apoptosis. These findings revealed that GTN subdues the P13K/AKT pathway and has auspicious chemopreventive and apoptotic actions in DEN-induced HCC. Therefore, GTN would be suggested as a new medicine in natural remedies for liver cancer.

通过抑制P13K/AKT信号通路,补骨脂素对二乙亚硝胺诱导的肝细胞癌具有化学预防潜力
肝癌是最致命的癌症,在全世界都有很高的死亡风险。Goniothalamin(GTN)是一种苯乙烯内酯,具有抗增殖和细胞凋亡活性。GTN 的分子作用尚未得到充分评估。因此,我们的研究旨在评估二乙基亚硝胺(DEN)诱导的大鼠肝细胞癌(HCC)的化学预防和细胞凋亡活性。大鼠被分为 4 组:对照组、仅 DEN 组、DEN + GTN(30 毫克/千克体重)组和仅 GTN(30 毫克/千克体重)组。我们对大鼠的体重、肝脏重量、肿瘤发病率、肝脏毒性标记物、抗氧化剂、炎症细胞因子、组织病理学、免疫组化和 Western 印迹进行了评估。DEN降低了体重、抗氧化剂和细胞凋亡,而提高了肿瘤发病率、毒性标志物、细胞因子和Bcl-2的表达。GTN 治疗可维持体重、肝脏重量和抗氧化剂水平,还能防止肿瘤发生、氧化应激、毒性标志物、促炎细胞因子和组织学变化。它通过抑制 Bcl-2 和提高 caspase-3 水平来触发细胞凋亡。GTN 还能减弱 P13K/ AKT 信号传导,从而增强细胞凋亡。这些研究结果表明,GTN 可抑制 P13K/AKT 通路,对 DEN 诱导的 HCC 具有良好的化学预防和细胞凋亡作用。因此,GTN可作为肝癌自然疗法的一种新药。
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来源期刊
Korean Journal of Physiology & Pharmacology
Korean Journal of Physiology & Pharmacology PHARMACOLOGY & PHARMACY-PHYSIOLOGY
CiteScore
3.20
自引率
5.00%
发文量
53
审稿时长
6-12 weeks
期刊介绍: The Korean Journal of Physiology & Pharmacology (Korean J. Physiol. Pharmacol., KJPP) is the official journal of both the Korean Physiological Society (KPS) and the Korean Society of Pharmacology (KSP). The journal launched in 1997 and is published bi-monthly in English. KJPP publishes original, peer-reviewed, scientific research-based articles that report successful advances in physiology and pharmacology. KJPP welcomes the submission of all original research articles in the field of physiology and pharmacology, especially the new and innovative findings. The scope of researches includes the action mechanism, pharmacological effect, utilization, and interaction of chemicals with biological system as well as the development of new drug targets. Theoretical articles that use computational models for further understanding of the physiological or pharmacological processes are also welcomed. Investigative translational research articles on human disease with an emphasis on physiology or pharmacology are also invited. KJPP does not publish work on the actions of crude biological extracts of either unknown chemical composition (e.g. unpurified and unvalidated) or unknown concentration. Reviews are normally commissioned, but consideration will be given to unsolicited contributions. All papers accepted for publication in KJPP will appear simultaneously in the printed Journal and online.
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