Natural Products as Anti-Angiogenic Agents: Molecular Targets, Signaling Pathways, and Mechanistic Insights.

IF 3.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Gajendra Singh Thakur, Sunny Rathee, Sakshi Soni, Vijay Pratap Ahirwar, Umesh K Patil
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引用次数: 0

Abstract

Angiogenesis, the process of forming new blood vessels from pre-existing vasculature, is a tightly regulated physiological process that is essential for embryonic development, wound healing, tissue regeneration, and the maintenance of normal tissue homeostasis. However, its pathological activation plays a pivotal role in tumor progression, chronic inflammation, and other angiogenesis-dependent diseases. Current antiangiogenic therapies, though clinically effective, are often limited by toxicity, resistance, and high costs. In this context, natural products have emerged as promising sources of bioactive molecules with potent antiangiogenic activity and minimal adverse effects. This review comprehensively discusses the molecular pathways underlying angiogenesis, including the regulatory roles of VEGF, FGF, HIF-1α, COX-2, NF-κB, and PI3K/Akt/mTOR cascades, and their modulation by natural compounds. Various phytoconstituents, including curcumin, resveratrol, quercetin, kaempferol, epigallocatechin gallate, withaferin A, betulinic acid, and marine- derived metabolites, exhibit anti-angiogenic activity by inhibiting endothelial cell proliferation, migration, and extracellular matrix degradation, while simultaneously downregulating key angiogenic signalling pathways. Structure-activity relationship (SAR) insights reveal that polyphenolic and terpenoid scaffolds play crucial roles in these mechanisms. The review also highlights experimental models used for anti-angiogenic evaluation and discusses clinical translation challenges related to bioavailability and formulation optimization. Overall, natural products represent a diverse and sustainable reservoir for developing next-generation antiangiogenic therapeutics, offering multi-targeted mechanisms and improved safety profiles suitable for cancer prevention and treatment.

作为抗血管生成剂的天然产物:分子靶点、信号通路和机制见解。
血管生成是由原有血管形成新血管的过程,是一个受到严格调控的生理过程,对胚胎发育、伤口愈合、组织再生和维持正常组织稳态至关重要。然而,它的病理激活在肿瘤进展、慢性炎症和其他血管生成依赖性疾病中起着关键作用。目前的抗血管生成疗法虽然在临床上有效,但往往受到毒性、耐药性和高成本的限制。在这种情况下,天然产物已成为生物活性分子的有希望的来源,具有强大的抗血管生成活性和最小的副作用。本文综述了血管生成的分子途径,包括VEGF、FGF、HIF-1α、COX-2、NF-κB和PI3K/Akt/mTOR级联的调控作用,以及它们在天然化合物中的调节作用。各种植物成分,包括姜黄素、白藜芦醇、槲皮素、山奈酚、表没食子儿茶素没食子酸酯、withaferin A、白桦酸和海洋衍生的代谢物,通过抑制内皮细胞增殖、迁移和细胞外基质降解,同时下调关键的血管生成信号通路,表现出抗血管生成活性。构效关系(SAR)揭示了多酚类和萜类支架在这些机制中起着至关重要的作用。该综述还强调了用于抗血管生成评估的实验模型,并讨论了与生物利用度和配方优化相关的临床翻译挑战。总的来说,天然产物代表了开发下一代抗血管生成疗法的多样化和可持续的储备,提供多靶向机制和改进的安全性,适合癌症预防和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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