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秦皮活性代谢产物可能的抗肿瘤作用及机制

The possible anti-tumor actions and mechanisms of active metabolites from Cortex Fraxini.

作者信息

Cai Bin, Cai Ting, Feng Zeyu, Zhu Huanhuan

机构信息

Department of Anorectal Surgery, Wuxi Hospital Affiliated to Nanjing University of Chinese Medicine, Wuxi, China.

Department of Nephrology, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi People's Hospital, Wuxi Medical Center, Wuxi, China.

出版信息

Front Pharmacol. 2024 Sep 13;15:1404172. doi: 10.3389/fphar.2024.1404172. eCollection 2024.

DOI:10.3389/fphar.2024.1404172
PMID:39346560
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11427270/
Abstract

Cortex Fraxini is a traditional Chinese herb that is widely available, inexpensive, and has low toxicity. Modern pharmacological studies have demonstrated that the active metabolites in Cortex Fraxini, including esculin, esculetin, and fraxetin, exert anti-tumor activities by regulating genes and proteins involved in cancer cell proliferation, apoptosis, invasion, and migration. Additionally, these metabolites play a pivotal role in the regulation of several tumor-associated signaling pathways, including the PI3K/Akt, MAPK/ERK, JAK/STAT3, and Wnt/β-catenin pathways. Due to their pro-apoptotic and anti-proliferative properties and , Cortex Fraxini and its active metabolites may be considered as potential candidates for the treatment of tumor. The aim of this review is to highlight the anti-tumor biological activities and underlying mechanisms of action of the active metabolites of Cortex Fraxini, with a view to providing a reference for their further development and application in the treatment of tumors.

摘要

秦皮是一种常见、价格低廉且毒性较低的传统中药。现代药理学研究表明,秦皮中的活性代谢产物,包括七叶苷、七叶亭和秦皮素,通过调节参与癌细胞增殖、凋亡、侵袭和迁移的基因和蛋白质发挥抗肿瘤活性。此外,这些代谢产物在调节几种肿瘤相关信号通路中起关键作用,包括PI3K/Akt、MAPK/ERK、JAK/STAT3和Wnt/β-连环蛋白通路。由于其促凋亡和抗增殖特性,秦皮及其活性代谢产物可被视为肿瘤治疗的潜在候选药物。本综述的目的是强调秦皮活性代谢产物的抗肿瘤生物学活性及其潜在作用机制,以期为其在肿瘤治疗中的进一步开发和应用提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df56/11427270/8dd9185f8e6c/fphar-15-1404172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df56/11427270/83114edf4b1a/fphar-15-1404172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df56/11427270/8dd9185f8e6c/fphar-15-1404172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df56/11427270/83114edf4b1a/fphar-15-1404172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df56/11427270/8dd9185f8e6c/fphar-15-1404172-g002.jpg

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本文引用的文献

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Fraxini cortex: Progresses in phytochemistry, pharmacology and ethnomedicinal uses.秦皮:植物化学、药理学和民族医学用途的进展。
J Ethnopharmacol. 2024 May 10;325:117849. doi: 10.1016/j.jep.2024.117849. Epub 2024 Feb 1.
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Targeting the RAS/RAF/MAPK pathway for cancer therapy: from mechanism to clinical studies.靶向 RAS/RAF/MAPK 通路治疗癌症:从机制到临床研究。
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and evaluation and anti-colitis activity of esculetin-loaded nanostructured lipid carrier decorated with DSPE-MPEG2000.
丁香苷负载的纳米结构脂质载体的评价及抗结肠炎活性,并用 DSPE-MPEG2000 进行修饰。
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Ki 67: a Promising Prognostic Marker in Early Breast Cancer-a Review Article.Ki-67:早期乳腺癌中一个有前景的预后标志物——一篇综述文章
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Fraxetin Interacts Additively with Cisplatin and Mitoxantrone, Antagonistically with Docetaxel in Various Human Melanoma Cell Lines-An Isobolographic Analysis.地蒽酚与顺铂和米托蒽醌呈相加作用,与多西他赛呈拮抗作用,在各种人黑色素瘤细胞系中——一种等辐射分析。
Int J Mol Sci. 2022 Dec 22;24(1):212. doi: 10.3390/ijms24010212.
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Fraxetin suppresses the proliferation, migration, and invasion of ovarian cancer cells by inhibiting the TLR4/STAT3 signaling pathway.法夏苷通过抑制 TLR4/STAT3 信号通路抑制卵巢癌细胞的增殖、迁移和侵袭。
Immunopharmacol Immunotoxicol. 2023 Jun;45(3):287-294. doi: 10.1080/08923973.2022.2141643. Epub 2022 Nov 8.
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The role of BCL-2 family proteins in regulating apoptosis and cancer therapy.BCL-2家族蛋白在调节细胞凋亡和癌症治疗中的作用。
Front Oncol. 2022 Oct 12;12:985363. doi: 10.3389/fonc.2022.985363. eCollection 2022.
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A comparative study of three chemometrics methods combined with excitation-emission matrix fluorescence for quantification of the bioactive compounds aesculin and aesculetin in Cortex Fraxini.三种化学计量学方法结合激发发射矩阵荧光法对秦皮中生物活性成分秦皮苷和秦皮素进行定量的比较研究。
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