从大戟科Croton velutinus (Euphorbiaceae)中提取的新型苯丙素作为潜在的抗癌天然产物靶向MAPKs:基于对接方法的综述。

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Renata A de Abrantes, Natalia F de Sousa, Ana Paula G M Farias, Samia S Duarte, Lucas S Abreu, Eudes S Velozo, Marcelo S da Silva, Pablo R da Silva, Josean F Tavares, Juan C R Gonçalves, Marcos T Scotti, Luciana Scotti, Marianna V Sobral
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引用次数: 0

摘要

癌症包括一组疾病,其特征是细胞生长不受控制,并且具有侵入或扩散到身体其他部位的能力。它被认为是一个重大的公共卫生问题,是全世界第二大死亡原因。丝裂原活化蛋白激酶(Mitogen- Activated Protein Kinase, MAPK)通路是许多癌症中发生改变的一个重要信号通路,它与细胞增殖、分化和存活的调控有关,在恶性肿瘤的发生和维持中起着核心作用。天然产物对药物治疗做出了重大贡献,特别是在癌症治疗领域。大戟科包括约300属和5000多个物种,以其丰富多样的生物活性化合物而闻名。Croton velutinus (Euphorbiaceae)是一种主要分布于巴西东北部的植物,最近由于从其根中分离出新的苯丙素而引起了人们的关注。其中,(E)-4-(1-环氧-7,8-丙烯)苯基苯甲酸酯(CV2)对多种人类肿瘤细胞系具有潜在的细胞毒活性,包括B16F10、MCF-7、HL60、HCT-116和HepG2。本文综述了从大戟科植物中提取的苯丙类化合物的抗肿瘤活性。此外,通过分子对接研究,我们探索了CV2与mapk (ERK, JNK, p38)的结合效果,并将其与文献中报道的其他25种苯丙类化合物进行了比较,揭示了有希望的相互作用,可以进一步研究其治疗应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Phenylpropanoid from Croton velutinus (Euphorbiaceae) as Potential Anticancer Natural Product Targeting MAPKs: Mini-review with Docking Approach.

Cancer encompasses a group of diseases characterized by uncontrolled cell growth and the ability to invade or spread to other parts of the body. It is considered a major public health issue, being the second leading cause of death worldwide. A crucial signaling pathway altered in many cancers is the Mitogen- Activated Protein Kinase (MAPK) pathway, which is associated with the regulation of cell proliferation, differentiation, and survival, playing a central role in the development and maintenance of malignant tumors. Natural products have made significant contributions to pharmacotherapy, particularly in the field of cancer treatment. The Euphorbiaceae family, comprising approximately 300 genera and over 5,000 species, is known for its rich diversity of bioactive compounds. Croton velutinus (Euphorbiaceae), a species predominantly found in Northeast Brazil, has recently garnered attention due to its novel phenylpropanoids isolated from its roots. Among these, (E)-4-(1-epoxy-7,8-propen) phenylbenzoate (CV2) has demonstrated potential cytotoxic activity against various human tumor cell lines, including B16F10, MCF-7, HL60, HCT-116, and HepG2. This mini-review aims to highlight the antitumor activity of phenylpropanoids derived from the Euphorbiaceae family. Furthermore, through molecular docking studies, we explored the binding efficacy of CV2 with MAPKs (ERK, JNK, p38), comparing it to 25 other phenylpropanoid compounds reported in the literature, revealing promising interactions that could be further investigated for therapeutic applications.

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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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