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黄芪甲苷的抗癌作用及其机制(综述)。

Anticancer effects and mechanisms of astragaloside‑IV (Review).

机构信息

Translational Research Laboratory for Stem Cell and Traditional Chinese Medicine, Innovation Institute for Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong 250355, P.R. China.

Laboratory for Stem Cell and Regenerative Medicine, Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital/Liaocheng University, Liaocheng, Shandong 252000, P.R. China.

出版信息

Oncol Rep. 2023 Jan;49(1). doi: 10.3892/or.2022.8442. Epub 2022 Nov 11.

DOI:10.3892/or.2022.8442
PMID:36367181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9685271/
Abstract

is widely used in Traditional Chinese Medicine to treat various cancers. Astragaloside‑IV (AS‑IV) is one of the major compounds isolated from and has been demonstrated to have antitumor effects by inhibiting cell proliferation, invasion and metastasis in various cancer types. Numerous studies have used cell culture and animal models of cancer to explore the antitumor activities of AS‑IV. In the present study, the antitumor effects and mechanisms of AS‑IV reported in studies recorded in the PubMed database were reviewed. First, the antitumor effects of AS‑IV on proliferation, cell cycle, apoptosis, autophagy, invasion, migration, metastasis and epithelial‑mesenchymal transition processes in cancer cells and the tumor microenvironment, including angiogenesis, tumor immunity and macrophage‑related immune responses to cancer cells, were comprehensively discussed. Subsequently, the molecular mechanisms and related signaling pathways associated with antitumor effects of AS‑IV as indicated by and studies were summarized, including the Wnt/AKT/GSK-3β (glycogen synthase kinase‑3β)/β‑catenin, TGF‑β/PI3K/AKT/mTOR, PI3K/MAPK/mTOR, PI3K/AKT/NF‑κB, Rac family small GTPase 1/RAS/MAPK/ERK, TNF‑α/protein kinase C/ERK1/2‑NF‑κB and Tregs (T‑regulatory cells)/IL‑11/STAT3 signaling pathways. Of note, several novel mechanisms of Toll‑like receptor 4 (TLR4)/NF‑κB/STAT3, pSmad3C/3L, nuclear factor erythroid 2‑related factor (NrF2)/heme oxygenase 1, circDLST/microRNA‑489‑3p/eukaryotic translation initiation factor 4A1 and macrophage‑related high‑mobility group box 1‑TLR4 signaling pathways associated with the anticancer activity of AS‑IV were also included. Finally, the limitations of current studies that must be addressed in future studies were pointed out to facilitate the establishment of AS‑IV as a potent therapeutic drug in cancer treatment.

摘要

黄芪甲苷(AS-IV)是从黄芪中分离得到的主要化合物之一,已被证明具有抑制多种癌症类型的细胞增殖、侵袭和转移的抗肿瘤作用。许多研究利用细胞培养和癌症动物模型探讨 AS-IV 的抗肿瘤活性。本研究对 PubMed 数据库中记录的 AS-IV 的抗肿瘤作用及其机制的研究进行了综述。首先,全面讨论了 AS-IV 对癌细胞和肿瘤微环境中增殖、细胞周期、凋亡、自噬、侵袭、迁移、转移和上皮-间充质转化过程的抗肿瘤作用,包括血管生成、肿瘤免疫和巨噬细胞相关的对癌细胞的免疫反应。随后,总结了 AS-IV 的抗肿瘤作用与其相关的分子机制及信号通路,这些通路是由细胞和动物研究表明的,包括 Wnt/AKT/GSK-3β(糖原合成酶激酶-3β)/β-catenin、TGF-β/PI3K/AKT/mTOR、PI3K/MAPK/mTOR、PI3K/AKT/NF-κB、Rac 家族小 GTPase 1/RAS/MAPK/ERK、TNF-α/蛋白激酶 C/ERK1/2-NF-κB 和 Tregs(调节性 T 细胞)/IL-11/STAT3 信号通路。值得注意的是,还包括了 Toll 样受体 4(TLR4)/NF-κB/STAT3、pSmad3C/3L、核因子红细胞 2 相关因子(NrF2)/血红素加氧酶 1、circDLST/miRNA-489-3p/真核起始因子 4A1 和巨噬细胞相关的高迁移率族蛋白 1-TLR4 信号通路与 AS-IV 的抗癌活性有关。最后,指出了当前研究中必须解决的局限性,以促进 AS-IV 作为癌症治疗中一种有效的治疗药物的建立。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/a7101dc53988/or-49-01-08442-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/528aed4ff190/or-49-01-08442-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/08f2a1ac3e40/or-49-01-08442-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/2592f373dca8/or-49-01-08442-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/a7101dc53988/or-49-01-08442-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/528aed4ff190/or-49-01-08442-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/08f2a1ac3e40/or-49-01-08442-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/2592f373dca8/or-49-01-08442-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b15/9685271/a7101dc53988/or-49-01-08442-g03.jpg

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