作为抗癌药物的人参皂苷 Rg5:关于机理、结构-活性关系和临床应用前景的全面综述。

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacological Reports Pub Date : 2024-04-01 Epub Date: 2024-03-25 DOI:10.1007/s43440-024-00586-5
Tilal Elsaman, Ali Mahmoud Muddathir, Ebtihal A M Mohieldin, Irmanida Batubara, Min Rahminiwati, Kosei Yamauchi, Magdi Awadalla Mohamed, Shadila Fira Asoka, Dietrich Büsselberg, Solomon Habtemariam, Javad Sharifi-Rad
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引用次数: 0

摘要

癌症仍然是世界上最主要的死亡原因之一。尽管传统治疗策略取得了巨大成功,但癌症的发病率和死亡率仍然居高不下,因此开发新的有效抗癌疗法已成为当务之急。人参皂苷 Rg5(Rg5)是一种只从人参中提取的次要人参皂苷成分,以其广泛的药理活性而著称。本文旨在全面综述 Rg5 的抗癌特性,重点关注其作用机制、结构-活性关系(SAR)和药代动力学属性。Rg5 的体外和体内活性已被证实可对抗多种癌症类型,如乳腺癌、肝癌、肺癌、骨癌和胃肠道癌。对癌症生长和存活至关重要的多种信号通路的调节介导了这些活性。然而,Rg5 的人体临床研究之前尚未涉及,其药代动力学特性仍相当模糊。此外,还发现 Rg5 的结构-活性关系(SAR)存在很大不足。因此,今后的工作重点应该是通过开展广泛的 SAR 研究来进一步优化 Rg5 的结构,从而发现 Rg5 具有强效抗癌活性所必需的结构特征。因此,本综述强调了 Rg5 作为潜在抗癌候选药物的价值,并指出了需要进一步调查的研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ginsenoside Rg5 as an anticancer drug: a comprehensive review on mechanisms, structure-activity relationship, and prospects for clinical advancement.

Cancer remains one of the leading causes of death in the world. Despite the considerable success of conventional treatment strategies, the incidence and mortality rates are still high, making developing new effective anticancer therapies an urgent priority. Ginsenoside Rg5 (Rg5) is a minor ginsenoside constituent obtained exclusively from ginseng species and is known for its broad spectrum of pharmacological activities. This article aimed to comprehensively review the anticancer properties of Rg5, focusing on action mechanisms, structure-activity relationship (SAR), and pharmacokinetics attributes. The in vitro and in vivo activities of Rg5 have been proven against several cancer types, such as breast, liver, lung, bone, and gastrointestinal (GI) cancers. The modulation of multiple signaling pathways critical for cancer growth and survival mediates these activities. Nevertheless, human clinical studies of Rg5 have not been addressed before, and there is still considerable ambiguity regarding its pharmacokinetics properties. In addition, a significant shortage in the structure-activity relationship (SAR) of Rg5 has been identified. Therefore, future efforts should focus on further optimization by performing extensive SAR studies to uncover the structural features essential for the potent anticancer activity of Rg5. Thus, this review highlights the value of Rg5 as a potential anticancer drug candidate and identifies the research areas requiring more investigation.

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来源期刊
Pharmacological Reports
Pharmacological Reports 医学-药学
CiteScore
8.40
自引率
0.00%
发文量
91
审稿时长
6 months
期刊介绍: Pharmacological Reports publishes articles concerning all aspects of pharmacology, dealing with the action of drugs at a cellular and molecular level, and papers on the relationship between molecular structure and biological activity as well as reports on compounds with well-defined chemical structures. Pharmacological Reports is an open forum to disseminate recent developments in: pharmacology, behavioural brain research, evidence-based complementary biochemical pharmacology, medicinal chemistry and biochemistry, drug discovery, neuro-psychopharmacology and biological psychiatry, neuroscience and neuropharmacology, cellular and molecular neuroscience, molecular biology, cell biology, toxicology. Studies of plant extracts are not suitable for Pharmacological Reports.
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