具有抗癌作用的天然黄酮类化合物橘皮素综述

Olalekan Bukunmi Ogunro , Oladimeji Taiwo Babatunde , Olufemi Samuel Araoyinbo
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引用次数: 0

摘要

目的由于现有治疗方法的耐药和不良副作用,寻求改进的癌症治疗方法仍在继续。黄酮类化合物提供了一个潜在的有前途的替代品,橘子素作为一种显著的具有抗癌作用的天然产物出现。stangeretin在阻止癌细胞进展方面显示出显著的潜力。它具有抗诱变特性,可以防止暴露于诱变剂后的癌症发展。此外,橙皮素可以破坏细胞周期,帮助DNA修复,降低癌症风险。它可以触发内源性和外源性凋亡通路,抑制肿瘤血管生成和转移,诱导自噬,同时减轻化疗引起的炎症。值得注意的是,橘皮素与紫杉醇、阿霉素和5-FU等化疗药物具有协同作用,增强了它们的疗效,并有可能克服耐药性。这些抗癌作用部分是通过调节信号通路如MAPK、Notch和PI3K/Akt/mtor来实现的。重要的是,橘皮素通过有效对抗各种类型的癌症显示出多功能性。这篇全面的综述强调了橘皮素多方面的药理学属性,并倡导将其纳入临床研究,作为抗癌疗法的一个有希望的补充,特别是与标准化疗药物联合使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tangeretin, a natural flavonoid with promising anticancer effects: A comprehensive review

Objectives

The search for improved cancer treatments continues due to drug resistance and adverse side effects of current therapies. Flavonoids offer a potentially promising alternative, with tangeretin emerging as a notable natural product with an anti-cancer effect.

Key findings

Tangeretin has shown remarkable potential in impeding cancer cell progression. It possesses antimutagenic properties and may prevent cancer development upon exposure to mutagens. Additionally, tangeretin disrupts the cell cycle, aids in DNA repair, and reduces cancer risk. It can trigger intrinsic and extrinsic apoptotic pathways, inhibit tumour angiogenesis and metastasis, and induce autophagy while alleviating inflammation caused by chemotherapy. Notably, tangeretin has demonstrated synergistic interactions with chemotherapeutic agents such as paclitaxel, doxorubicin, and 5-FU, enhancing their efficacy and potentially overcoming drug resistance. These anticancer effects are partly achieved through modulation of signalling pathways like MAPK, Notch, and PI3K/Akt/mtor. Importantly, tangeretin exhibits versatility by effectively combating various cancer types.

Summary

This comprehensive review underscores tangeretin’s multifaceted pharmacological attributes and advocates for its inclusion in clinical studies as a promising addition to the arsenal of cancer-fighting therapies, particularly in combination with standard chemotherapeutics.
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