Flavonoid-Mediated Suppression of Tumor Angiogenesis: Roles of Ang-Tie/PI3K/AKT.

IF 2.7 Q2 PATHOLOGY Pathophysiology Pub Date : 2024-10-12 DOI:10.3390/pathophysiology31040043
Shallu Saini, Hardeep Singh Tuli, Reena V Saini, Adesh K Saini, Katrin Sak, Damandeep Kaur, Moyad Shahwan, Ritu Chauhan, Abhishek Chauhan
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Abstract

Angiogenesis is a process involved in the formation of new blood capillaries from pre-existing ones. It is regulated by several anti-angiogenic molecules involved in tumor growth and metastasis. The endothelial angiopoietin Ang-Tie/PI3K/AKT growth receptor pathway is necessary for healthy vascular development. The activation of AKT is controlled by a multistep process involving phosphoinositide 3-kinase (PI3K). This article aims to provide an overview of the role and mechanism of the Ang-Tie/PI3K/AKT signaling pathways and the potential of flavonoids as anti-angiogenic drugs. Flavonoids have shown great potential in preventing angiogenesis by targeting signaling pathways and exhibit additional anti-cancer properties. Research studies have revealed that the currently available anti-angiogenic drugs do not meet the safety and efficacy standards for treating tumor growth. Phytocompounds have long been a valuable resource for the development of novel therapeutic drugs. This article explores recent findings explaining the role and mechanism of the Ang-Tie/PI3K/AKT signaling pathways, as well as the interaction of flavonoids with angiogenic signaling pathways as a novel therapeutic approach. Several investigations have shown that synergistic studies of natural phytocompounds have great potential to target these pathways to inhibit tumor growth. Therefore, flavonoid-based medications may offer a more effective synergistic strategy to treat cancer.

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类黄酮介导的肿瘤血管生成抑制:Ang-Tie/PI3K/AKT的作用
血管生成是由原有毛细血管形成新毛细血管的过程。它受到几种参与肿瘤生长和转移的抗血管生成分子的调控。内皮血管生成素 Ang-Tie/PI3K/AKT 生长受体途径是血管健康发育所必需的。AKT 的活化由磷酸肌酸 3- 激酶(PI3K)参与的多步骤过程控制。本文旨在概述 Ang-Tie/PI3K/AKT 信号通路的作用和机制,以及类黄酮作为抗血管生成药物的潜力。黄酮类化合物在通过靶向信号通路防止血管生成方面显示出巨大潜力,并具有其他抗癌特性。研究发现,目前可用的抗血管生成药物在治疗肿瘤生长方面并不符合安全性和有效性标准。植物化合物一直以来都是开发新型治疗药物的宝贵资源。本文探讨了解释 Ang-Tie/PI3K/AKT 信号通路的作用和机制的最新发现,以及黄酮类化合物作为一种新型治疗方法与血管生成信号通路的相互作用。多项研究表明,天然植物化合物的协同研究在针对这些通路抑制肿瘤生长方面具有巨大潜力。因此,基于类黄酮的药物可能为治疗癌症提供更有效的协同策略。
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来源期刊
Pathophysiology
Pathophysiology Medicine-Pathology and Forensic Medicine
CiteScore
3.10
自引率
0.00%
发文量
48
期刊介绍: Pathophysiology is an international journal which publishes papers in English which address the etiology, development, and elimination of pathological processes. Contributions on the basic mechanisms underlying these processes, model systems and interdisciplinary approaches are strongly encouraged.
期刊最新文献
Correction: Yamarthi et al. Sepia pharaonis Ink Mitigates Dehydroepiandrosterone-Induced Insulin Resistance in Mouse Model of Polycystic Ovarian Syndrome. Pathophysiology 2024, 31, 408-419. Cause of Death Analysis in a 9½-Year-Old with COVID-19 and Dravet Syndrome. Evaluation of Creatine Monohydrate Supplementation on the Gastrocnemius Muscle of Mice with Muscular Dystrophy: A Preliminary Study. Hepatic Estrogen Receptor Alpha Overexpression Protects Against Hepatic Insulin Resistance and MASLD. Low Renalase Levels in Newly Diagnosed CML: Dysregulation Sensitive to Modulation by Tyrosine Kinase Inhibitors.
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