The Medicinal Chemistry of Cyanidin and its Glycoside Derivatives: Focus on the Antiproliferative and Potential Anticancer Activity.

IF 2.1 4区 医学 Q3 CHEMISTRY, MEDICINAL
Planta medica Pub Date : 2025-06-12 DOI:10.1055/a-2634-4300
Abdur Rauf, Ahmed Olatunde, Rahaf Ajaj, Nabia Hafeez, Mohamed Y Zaky, Rezaul Islam, Md Mozahidul Islam, Giovanni Ribaudo
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引用次数: 0

Abstract

Cyanidin and its glucosides are anthocyanins belonging to the class of flavonoid phytochemicals. These pigments give fruits and vegetables their typical reddish-purple nuance, and their peculiar chemical features result in a remarkable ability to neutralize reactive oxygen species and other mutagens. Thus, both cyanidin and its glycosides were proposed as candidates for chemoprevention, as anticancer agents and as adjuvant therapies. Indeed, the compounds were investigated through various in vitro and in vivo models of colon, breast, kidney, prostate and liver cancer and glioma. Cyanidin and its derivatives have been found to inhibit key signaling pathways, such as PI3K/Akt, MAPK, and NF-κB, which can reduce cancer cell growth, induce apoptosis, and suppress metastasis. In the first part of the review, the chemical properties of cyanidin and its glycoside analogues will be discussed. Then, an overview of in vitro evidence on activity will be presented, followed by a report on preclinical and clinical data together with comments on the involved mechanisms. Eventually, the aspect of pharmacokinetic properties, bioavailability and formulation will be dissected. Overall, the review indicates that cyanidin and its derivatives could be effective anticancer agents but also calls for a deeper understanding of the molecular mechanisms underlying their bioactivity. Despite promising results, resolving issues like stability, absorption, and targeted distribution is crucial to maximize their therapeutic potential. More research is needed to develop innovative cyanidin-based formulations for efficient cancer treatment.

花青素及其苷类衍生物的药物化学研究:以其抗增殖和潜在的抗癌活性为重点。
花青素及其糖苷是类黄酮类植物化学物质中的花青素类。这些色素使水果和蔬菜呈现出典型的红紫色,它们独特的化学特性使它们具有非凡的中和活性氧和其他诱变剂的能力。因此,花青素及其糖苷被认为是化学预防、抗癌和辅助治疗的候选药物。事实上,这些化合物通过各种体外和体内模型进行了结肠癌、乳腺癌、肾癌、前列腺癌、肝癌和胶质瘤的研究。研究发现,花青素及其衍生物可抑制PI3K/Akt、MAPK、NF-κB等关键信号通路,从而抑制癌细胞生长、诱导凋亡、抑制转移。第一部分综述了花青素及其糖苷类似物的化学性质。然后,将概述有关活性的体外证据,随后是临床前和临床数据的报告以及对相关机制的评论。最后,将对其药代动力学特性、生物利用度和配方进行分析。综上所述,该综述表明花青素及其衍生物可能是有效的抗癌药物,但也需要对其生物活性的分子机制有更深入的了解。尽管结果令人鼓舞,但解决稳定性、吸收和靶向分布等问题对于最大限度地发挥其治疗潜力至关重要。需要更多的研究来开发创新的基于花青素的配方,以有效地治疗癌症。
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来源期刊
Planta medica
Planta medica 医学-药学
CiteScore
5.10
自引率
3.70%
发文量
101
审稿时长
1.8 months
期刊介绍: Planta Medica is one of the leading international journals in the field of natural products – including marine organisms, fungi as well as micro-organisms – and medicinal plants. Planta Medica accepts original research papers, reviews, minireviews and perspectives from researchers worldwide. The journal publishes 18 issues per year. The following areas of medicinal plants and natural product research are covered: -Biological and Pharmacological Activities -Natural Product Chemistry & Analytical Studies -Pharmacokinetic Investigations -Formulation and Delivery Systems of Natural Products. The journal explicitly encourages the submission of chemically characterized extracts.
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