LAQV-REQUIMTE, Department of Chemistry, University of Aveiro, 3810-193, Aveiro, Portugal.
CITAB Inov4Agro - Institute for Innovation, Capacity Building and Sustainability of Agri-food Production, University of Trás-os-Montes and Alto Douro (UTAD), 5000-801, Vila Real, Portugal.
Med Oncol. 2024 Aug 17;41(9):228. doi: 10.1007/s12032-024-02467-6.
Moscatilin, a bibenzyl derivative from the Dendrobium genus, has been traditionally used in Chinese medicine. Recent studies suggest its potential as a powerful anticancer agent due to its diverse pharmacological properties.This review aims to consolidate current research on moscatilin's anticancer mechanisms, structure-activity relationships, and therapeutic potential to assess its viability for clinical use. A literature search was performed in PubMed/MedLine, Scopus, and Web of Science.The search focused on "cancer," "moscatilin," "anticancer," "bioactivity," "dendrobium," and "pharmacological properties." Relevant studies on molecular mechanisms, preclinical and clinical efficacy, and bioavailability were reviewed. Moscatilin exhibits significant anticancer effects in lung, breast, colorectal, and pancreatic cancers. It induces apoptosis via the JNK/SAPK pathway, inhibits cell proliferation, and suppresses metastasis. Structure-activity relationship studies reveal that phenolic groups and a two-carbon bridge are crucial for its efficacy. Additionally, moscatilin shows good bioavailability and a favorable safety profile, with low toxicity to healthy cells. Moscatilin demonstrates considerable potential as an anticancer agent, targeting multiple cancer progression pathways. Further clinical trials are essential to confirm its therapeutic efficacy and safety in humans.
美商楼氏(Moscatilin)是一种来自石斛属的双苄基衍生物,在传统中药中被广泛使用。最近的研究表明,由于其多种药理学特性,它可能具有强大的抗癌作用。本综述旨在整合美商楼氏的抗癌机制、结构-活性关系和治疗潜力的现有研究,以评估其在临床应用中的可行性。在 PubMed/MedLine、Scopus 和 Web of Science 中进行了文献检索。搜索重点是“癌症”、“美商楼氏”、“抗癌”、“生物活性”、“石斛”和“药理学特性”。综述了有关分子机制、临床前和临床疗效以及生物利用度的相关研究。美商楼氏在肺癌、乳腺癌、结直肠癌和胰腺癌中表现出显著的抗癌作用。它通过 JNK/SAPK 途径诱导细胞凋亡,抑制细胞增殖,并抑制转移。结构-活性关系研究表明,酚基团和两个碳原子桥对于其功效至关重要。此外,美商楼氏具有良好的生物利用度和良好的安全性,对健康细胞的毒性较低。美商楼氏作为一种抗癌剂具有相当大的潜力,可针对多种癌症进展途径。需要进一步的临床试验来确认其在人类中的治疗效果和安全性。