Moscatilin, a potential therapeutic agent for cancer treatment: insights into molecular mechanisms and clinical prospects.

IF 2.8 4区 医学 Q2 ONCOLOGY Medical Oncology Pub Date : 2024-08-17 DOI:10.1007/s12032-024-02467-6
Rita Silva-Reis, Vera L M Silva, Susana M Cardoso, Izabela Michalak, Mirosława Püsküllüoğlu, Daniela Calina, Javad Sharifi-Rad
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Abstract

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.

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麝香草苷--一种潜在的癌症治疗药物:对分子机制和临床前景的见解。
莫斯卡替林(Moscatilin)是一种来自铁皮石斛属植物的双苄基衍生物,历来被用于中药中。本综述旨在整合目前有关莫斯卡替林的抗癌机制、结构-活性关系和治疗潜力的研究,以评估其临床应用的可行性。我们在 PubMed/MedLine、Scopus 和 Web of Science 中进行了文献检索,重点是 "癌症"、"莫斯卡替林"、"抗癌"、"生物活性"、"铁皮石斛 "和 "药理特性"。对分子机制、临床前和临床疗效以及生物利用度方面的相关研究进行了综述。莫斯卡替林对肺癌、乳腺癌、结肠直肠癌和胰腺癌有显著的抗癌作用。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,酚基和双碳桥对其药效至关重要。此外,莫斯卡替林还具有良好的生物利用度和安全性,对健康细胞的毒性很低。莫斯卡替林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。进一步的临床试验对于确认其在人体中的疗效和安全性至关重要。
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
Medical Oncology
Medical Oncology 医学-肿瘤学
CiteScore
4.20
自引率
2.90%
发文量
259
审稿时长
1.4 months
期刊介绍: Medical Oncology (MO) communicates the results of clinical and experimental research in oncology and hematology, particularly experimental therapeutics within the fields of immunotherapy and chemotherapy. It also provides state-of-the-art reviews on clinical and experimental therapies. Topics covered include immunobiology, pathogenesis, and treatment of malignant tumors.
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