Department of Chemistry, NMAM Institute of Technology (NMAMIT), Nitte (Deemed to Be University), Nitte, Mangaluru, India.
Departamento de Farmacia, Facultad de Química, Universidad Nacional Autónoma de México, 04510, Ciudad de Mexico, Mexico.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Sep;397(9):6317-6336. doi: 10.1007/s00210-024-03095-7. Epub 2024 Apr 23.
Arnicolide D, a potent sesquiterpene lactone from Centipeda minima, has emerged as a promising anticancer candidate, demonstrating significant efficacy in inhibiting cancer cell proliferation, inducing apoptosis, and suppressing metastasis across various cancer models. This comprehensive study delves into the molecular underpinnings of Arnicolide D's anticancer actions, emphasizing its impact on key signaling pathways such as PI3K/AKT/mTOR and STAT3, and its role in modulating cell cycle and survival mechanisms. Quantitative data from preclinical studies reveal Arnicolide D's dose-dependent cytotoxicity against cancer cell lines, including nasopharyngeal carcinoma, triple-negative breast cancer, and human colon carcinoma, showcasing its broad-spectrum anticancer potential. Given its multifaceted mechanisms and preclinical efficacy, Arnicolide D warrants further investigation in clinical settings to validate its therapeutic utility against cancer. The evidence presented underscores the need for rigorous pharmacokinetic and toxicological studies to establish safe dosing parameters for future clinical trials.
千里光宁 D,一种来自千里光的强效倍半萜内酯,已成为一种很有前途的抗癌候选药物,在抑制癌细胞增殖、诱导细胞凋亡和抑制多种癌症模型中的转移方面显示出显著的疗效。这项全面的研究深入探讨了千里光宁 D 的抗癌作用的分子基础,强调了它对 PI3K/AKT/mTOR 和 STAT3 等关键信号通路的影响,以及它在调节细胞周期和存活机制中的作用。来自临床前研究的定量数据显示,千里光宁 D 对癌细胞系具有剂量依赖性的细胞毒性,包括鼻咽癌、三阴性乳腺癌和人结肠癌细胞系,展示了其广谱抗癌潜力。鉴于其多方面的机制和临床前疗效,千里光宁 D 值得在临床环境中进一步研究,以验证其对癌症的治疗效用。所呈现的证据强调了需要进行严格的药代动力学和毒理学研究,为未来的临床试验确定安全的剂量参数。