类黄酮分子对肝癌中PI3K/AKT/mTOR级联反应的调控

IF 3.5 4区 医学 Q3 ONCOLOGY
Asma Naqi, Mohammad Ahmed Khan, Zehra Khatoon, Uzma Bano, Javed Ali, Mohd Akhtar, Mohd Mujeeb, Abul Kalam Najmi
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引用次数: 0

摘要

肝细胞癌(HCC)是全球癌症死亡的主要原因之一。磷脂酰肌醇-3-激酶/蛋白激酶B/哺乳动物雷帕霉素靶蛋白(PI3K/AKT/mTOR)信号通路是细胞中高度调控的促进细胞存活、生长、运动、代谢和增殖的信号转导通路之一。该信号轴在多种肿瘤中异常激活,如乳腺、宫颈、结肠、胃、肝、肺、卵巢和前列腺。在⁓50%的HCC病例中,PI3K/AKT/mTOR (PAM)信号轴是最关键且过度激活的信号通路。植物化学物质,如黄酮类化合物,迄今已被鉴定和分离,据报道具有抗癌、保护心脏、抗炎、抗氧化和保护肝脏的特性。方法:本综述中讨论的研究从PubMed、Scopus和谷歌Scholar数据库中获得,使用与HCC和类黄酮相关的术语组合。结果:本文对黄酮类化合物的作用机制进行综述,以进一步了解其在HCC中的作用。它还讨论了利用各种类黄酮片段靶向PAM通路的机制途径。讨论:科学文献描述了各种黄酮类化合物靶向“PAM轴”以控制肝癌发生的药理学方面。这些类黄酮使靶标化学敏感化,从而减少对化疗的抗性,同时也作为直接抗氧化剂、间接抗氧化剂或促氧化剂。结论:黄酮类化合物在肝细胞癌治疗中具有抑制PAM通路的巨大潜力,需要进一步研究其药代动力学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of the PI3K/AKT/mTOR cascade in Hepatocellular Carcinoma Using Flavonoid Molecules.

Introduction: Hepatocellular carcinoma (HCC) is one of the leading causes of global cancer death. The phosphatidylinositol-3-kinase/ protein kinase B/ mammalian target of rapamycin (PI3K/AKT/mTOR) signalling pathway is one of the highly regulated signalling transduction pathways in cells promoting cell survival, growth, motility, metabolism, and proliferation. This signalling axis is aberrantly activated in a wide variety of tumours, such as breast, cervical, colon, gastric, liver, lung, ovarian, and prostate. The PI3K/AKT/mTOR (PAM) signalling axis is the most pivotal and overactivated signalling pathway in ⁓50% of HCC cases. Phytochemicals, such as flavonoids, have been identified and isolated to date and are reported to have anticancer, cardioprotective, anti-inflammatory, anti-oxidant, and hepato-protective properties.

Methods: Studies discussed in this review were obtained from PubMed, Scopus, and Google Scholar databases using combinations of the terms related to HCC and flavonoids.

Results: This review summarizes the mechanism of action of flavonoids to get a better understanding of their role in HCC. It also discusses mechanistic approaches for targeting the PAM pathway using various flavonoid moieties.

Discussion: The scientific literature describes the pharmacological aspect of various flavonoids in targeting the "PAM axis" to manage hepatocarcinogenesis. These flavonoids chemo-sensitize the target, thus reducing the chance of resistance towards the chemotherapy, and also act as direct antioxidants, indirect antioxidants, or pro-oxidants.

Conclusion: Further studies are required to investigate the pharmacokinetic profile of flavonoids as they hold immense potential to inhibit the PAM pathway in the management of hepatocellular carcinoma.

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来源期刊
Current cancer drug targets
Current cancer drug targets 医学-肿瘤学
CiteScore
5.40
自引率
0.00%
发文量
105
审稿时长
1 months
期刊介绍: Current Cancer Drug Targets aims to cover all the latest and outstanding developments on the medicinal chemistry, pharmacology, molecular biology, genomics and biochemistry of contemporary molecular drug targets involved in cancer, e.g. disease specific proteins, receptors, enzymes and genes. Current Cancer Drug Targets publishes original research articles, letters, reviews / mini-reviews, drug clinical trial studies and guest edited thematic issues written by leaders in the field covering a range of current topics on drug targets involved in cancer. As the discovery, identification, characterization and validation of novel human drug targets for anti-cancer drug discovery continues to grow; this journal has become essential reading for all pharmaceutical scientists involved in drug discovery and development.
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