Targeting telomere dynamics with plant-derived compounds: Molecular strategies against aging

Q2 Agricultural and Biological Sciences
Raushanara Akter, Adwiza Chakraborty Bishakha, Raisha Rajib, Asef Raj, Mashwiyat Samrin Roja, Fouzia Noor
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引用次数: 0

Abstract

Telomeres, the repetitive DNA–protein complexes capping eukaryotic chromosomes, preserve genomic stability and regulate cellular replicative capacity. Progressive telomere shortening, coupled with diminished telomerase activity, is a hallmark of aging and contributes to cellular senescence, tissue degeneration, and the onset of age-related diseases. Conversely, telomerase overactivation in malignant cells enables uncontrolled proliferation, positioning telomere biology as a dual therapeutic target in longevity and oncology. Plant-derived compounds possess diverse structural classes such as polyphenols, flavonoids, triterpenoid saponins, polysaccharides, lignans, alkaloids, carotenoids, amino acids, and fatty acids that can modulate telomere length and telomerase activity via multiple molecular pathways. These include antioxidant and anti-inflammatory actions, regulation of key genes such as hTERT, SIRT1, and c-Myc, modulation of PI3K/Akt, JAK/STAT, and ERK signaling, and stabilization or destabilization of G-quadruplex DNA structures. Compounds such as resveratrol, epigallocatechin gallate, astragaloside IV, cycloastragenol, and ginsenoside Rg1 have demonstrated telomerase activation or inhibition in a context-dependent manner, influenced by concentration, cell type, and disease state. This review categorizes plant-derived positive and negative telomere/telomerase modulators, detailing their sources, mechanisms of action, experimental evidence, and the formulation challenges that hinder clinical translation, such as low bioavailability, instability, and variability in phytochemical content. By integrating molecular insights with pharmacological perspectives, this review highlights the potential of plant-derived agents as multi-target interventions in aging and cancer. Advancing this field will require rigorous pharmacokinetic profiling, standardized preparations, and longitudinal clinical studies to bridge the gap between laboratory findings and real-world therapeutic outcomes.

Abstract Image

用植物源性化合物靶向端粒动力学:抗衰老的分子策略
端粒是覆盖在真核生物染色体上的重复dna -蛋白质复合物,它保持基因组的稳定性并调节细胞的复制能力。进行性端粒缩短,加上端粒酶活性降低,是衰老的标志,并有助于细胞衰老,组织变性和年龄相关疾病的发病。相反,端粒酶在恶性细胞中的过度激活会导致不受控制的增殖,使端粒生物学成为长寿和肿瘤的双重治疗靶点。植物源性化合物具有多种结构类别,如多酚、类黄酮、三萜皂苷、多糖、木脂素、生物碱、类胡萝卜素、氨基酸和脂肪酸,它们可以通过多种分子途径调节端粒长度和端粒酶活性。这些包括抗氧化和抗炎作用,关键基因如hTERT、SIRT1和c-Myc的调节,PI3K/Akt、JAK/STAT和ERK信号的调节,以及g -四重体DNA结构的稳定或不稳定。诸如白藜芦醇、表没食子儿茶素没食子酸酯、黄芪甲苷IV、环黄芪醇和人参皂苷Rg1等化合物已经证明端粒酶的激活或抑制以依赖于环境的方式进行,受浓度、细胞类型和疾病状态的影响。本文对植物源性端粒/端粒酶阳性和阴性调节剂进行了分类,详细介绍了它们的来源、作用机制、实验证据以及阻碍临床转化的配方挑战,如低生物利用度、不稳定性和植物化学含量的可变性。通过结合分子和药理学的观点,本综述强调了植物源性药物作为多靶点干预衰老和癌症的潜力。推进这一领域将需要严格的药代动力学分析、标准化的制剂和纵向临床研究,以弥合实验室发现和现实世界治疗结果之间的差距。
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
Current Research in Pharmacology and Drug Discovery
Current Research in Pharmacology and Drug Discovery Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
6.40
自引率
0.00%
发文量
65
审稿时长
40 days
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