• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

中药 化学成分、抗肿瘤作用机制及其临床应用:全面综述

Chemical Constituents, Anti-Tumor Mechanisms, and Clinical Application: A Comprehensive Review on .

机构信息

School Basic Medical Sciences, Heilongjiang University of Chinese Medicine, 24 Heping Road, Harbin 150040, China.

出版信息

Molecules. 2024 Aug 31;29(17):4134. doi: 10.3390/molecules29174134.

DOI:10.3390/molecules29174134
PMID:39274982
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11397148/
Abstract

With the increasing global incidence and mortality rates of cancer, the development of novel anti-tumor drugs has become particularly urgent. D. Don, a perennial herb belonging to the genus Scutellaria in the family Lamiaceae, has aroused extensive attention for its medicinal value in recent years. This article presents an exhaustive review of the flavonoid, diterpene, and other chemical constituents harbored within , delving into the intricate mechanisms by which these compounds orchestrate their anti-tumor effects via diverse biological pathways. Remarkably, these compounds distinguish themselves through their capability to regulate cellular signaling, inhibit cancer cell proliferation, trigger apoptosis, disrupt angiogenesis, and bolster immune responses. These anti-tumor effects are achieved through strategic modulation of pivotal signaling cascades, particularly the PI3K/Akt/mTOR, MAPK, and NFκB pathways. In addition, this article also summarizes the clinical applications of in tumor treatment, especially its potential in alleviating the side effects of radiotherapy and chemotherapy and improving patients' quality of life. In conclusion, this review comprehensively summarizes and analyzes the chemical constituents, anti-tumor mechanisms, and clinical applications of , with the aim of systematically reviewing the existing research results and exploring potential future research directions.

摘要

随着癌症在全球的发病率和死亡率不断上升,新型抗肿瘤药物的开发变得尤为迫切。丹参,唇形科黄芩属多年生草本植物,近年来因其药用价值而引起广泛关注。本文对丹参中的黄酮类、二萜类等化学成分进行了全面综述,深入探讨了这些化合物通过多种生物途径发挥抗肿瘤作用的复杂机制。值得注意的是,这些化合物通过调节细胞信号、抑制癌细胞增殖、诱导细胞凋亡、破坏血管生成和增强免疫反应来发挥其抗肿瘤作用。这些抗肿瘤作用是通过对关键信号通路的策略性调节来实现的,特别是 PI3K/Akt/mTOR、MAPK 和 NFκB 通路。此外,本文还总结了丹参在肿瘤治疗中的临床应用,特别是其在减轻放化疗副作用和提高患者生活质量方面的潜力。总之,本文全面总结和分析了丹参的化学成分、抗肿瘤机制和临床应用,旨在系统回顾现有研究成果并探索潜在的未来研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/44adedba7558/molecules-29-04134-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/6933e9ba6f88/molecules-29-04134-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/4f8b0a17d2b9/molecules-29-04134-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/384bb458b058/molecules-29-04134-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/c07b134b6c5f/molecules-29-04134-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/9d801b102446/molecules-29-04134-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/0f250c4abf3e/molecules-29-04134-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/44adedba7558/molecules-29-04134-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/6933e9ba6f88/molecules-29-04134-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/4f8b0a17d2b9/molecules-29-04134-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/384bb458b058/molecules-29-04134-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/c07b134b6c5f/molecules-29-04134-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/9d801b102446/molecules-29-04134-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/0f250c4abf3e/molecules-29-04134-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e3/11397148/44adedba7558/molecules-29-04134-g007.jpg

相似文献

1
Chemical Constituents, Anti-Tumor Mechanisms, and Clinical Application: A Comprehensive Review on .中药 化学成分、抗肿瘤作用机制及其临床应用:全面综述
Molecules. 2024 Aug 31;29(17):4134. doi: 10.3390/molecules29174134.
2
Anti-tumor effect of Scutellaria barbata D. Don extracts on ovarian cancer and its phytochemicals characterisation.半枝莲提取物对卵巢癌的抗肿瘤作用及其植物化学成分分析
J Ethnopharmacol. 2017 Jul 12;206:184-192. doi: 10.1016/j.jep.2017.05.032. Epub 2017 May 29.
3
A review of the ethnopharmacology, phytochemistry, pharmacology, and quality control of Scutellaria barbata D. Don.《夏枯草 D. Don 的民族药理学、植物化学、药理学和质量控制研究综述》
J Ethnopharmacol. 2020 May 23;254:112260. doi: 10.1016/j.jep.2019.112260. Epub 2019 Sep 29.
4
Antitumor and anti-angiogenic activities of Scutellaria barbata extracts in vitro are partially mediated by inhibition of Akt/protein kinase B.体外黄芩提取物的抗肿瘤和抗血管生成活性部分是通过抑制 Akt/蛋白激酶 B 介导的。
Mol Med Rep. 2012 Mar;5(3):788-92. doi: 10.3892/mmr.2011.694. Epub 2011 Dec 6.
5
Ethyl Acetate Fraction from Hedyotis Diffusa Plus Scutellaria Barbata Inhibits the Progression of Breast Cancer Targeting LMO1 and AKT/Mtor Signaling Pathway.白花蛇舌草乙酸乙酯部位联合半枝莲抑制 LMO1 和 AKT/mTOR 信号通路抑制乳腺癌的进展。
Comb Chem High Throughput Screen. 2024;27(12):1735-1744. doi: 10.2174/1386207326666230913105858.
6
Regulation of IGF-I production and proliferation of human leiomyomal smooth muscle cells by Scutellaria barbata D. Don in vitro: isolation of flavonoids of apigenin and luteolin as acting compounds.半枝莲对人子宫平滑肌瘤平滑肌细胞IGF-I生成及增殖的体外调控作用:芹菜素和木犀草素黄酮类活性成分的分离鉴定
Toxicol Appl Pharmacol. 2005 Jun 15;205(3):213-24. doi: 10.1016/j.taap.2004.10.007.
7
Scutellaria barbata D. Don inhibits tumor angiogenesis via suppression of Hedgehog pathway in a mouse model of colorectal cancer.半枝莲通过抑制结直肠癌小鼠模型中的Hedgehog信号通路来抑制肿瘤血管生成。
Int J Mol Sci. 2012;13(8):9419-9430. doi: 10.3390/ijms13089419. Epub 2012 Jul 25.
8
Scutellaria Barbata D Don Inhibits Colorectal Cancer Growth via Suppression of Multiple Signaling Pathways.半枝莲通过抑制多种信号通路抑制结直肠癌生长。
Integr Cancer Ther. 2014 May;13(3):240-8. doi: 10.1177/1534735413508811. Epub 2013 Nov 13.
9
Scutellaria barbata: A Review on Chemical Constituents, Pharmacological Activities and Clinical Applications.半枝莲:化学成分、药理活性及临床应用综述。
Curr Pharm Des. 2020;26(1):160-175. doi: 10.2174/1381612825666191216124310.
10
Enhanced anticancer effects of Scutellaria barbata D. Don in combination with traditional Chinese medicine components on non-small cell lung cancer cells.黄芩与中药成分联合增强对非小细胞肺癌细胞的抗癌作用。
J Ethnopharmacol. 2018 May 10;217:140-151. doi: 10.1016/j.jep.2018.02.020. Epub 2018 Feb 16.

引用本文的文献

1
Exploring the active ingredients of Banzhilian and its mechanism of action on diabetic Gastric cancer based on network pharmacology.基于网络药理学探究半枝莲治疗糖尿病性胃癌的活性成分及其作用机制
Sci Rep. 2025 Apr 28;15(1):14808. doi: 10.1038/s41598-025-98214-6.
2
Recent advancement in the anticancer efficacy of the natural flavonoid scutellarin: a comprehensive review.天然黄酮类化合物灯盏花素抗癌疗效的最新进展:综述
Front Pharmacol. 2025 Mar 27;16:1579609. doi: 10.3389/fphar.2025.1579609. eCollection 2025.

本文引用的文献

1
Drug repurposing for cancer.癌症的药物重新利用
Prog Mol Biol Transl Sci. 2024;207:123-150. doi: 10.1016/bs.pmbts.2024.03.032. Epub 2024 May 11.
2
Network-based pharmacology-based research on the effect and mechanism of the Hedyotis diffusa-Scutellaria Barbata pair in the treatment of hepatocellular carcinoma.基于网络药理学的白花蛇舌草-半枝莲药对治疗肝细胞癌作用及机制研究。
Sci Rep. 2024 Jan 10;14(1):963. doi: 10.1038/s41598-023-50696-y.
3
Exploration of the effect and mechanism of Scutellaria barbata D. Don in the treatment of ovarian cancer based on network pharmacology and in vitro experimental verification.
基于网络药理学和体外实验验证探讨黄芩治疗卵巢癌的作用及机制。
Medicine (Baltimore). 2023 Dec 22;102(51):e36656. doi: 10.1097/MD.0000000000036656.
4
Mechanisms of Traditional Chinese medicine/natural medicine in HR-positive Breast Cancer: A comprehensive Literature Review.中药/天然药物治疗人表皮生长因子受体 2 阳性乳腺癌的作用机制:全面的文献综述。
J Ethnopharmacol. 2024 Jan 30;319(Pt 3):117322. doi: 10.1016/j.jep.2023.117322. Epub 2023 Oct 20.
5
Ethyl Acetate Fraction from Hedyotis Diffusa Plus Scutellaria Barbata Inhibits the Progression of Breast Cancer Targeting LMO1 and AKT/Mtor Signaling Pathway.白花蛇舌草乙酸乙酯部位联合半枝莲抑制 LMO1 和 AKT/mTOR 信号通路抑制乳腺癌的进展。
Comb Chem High Throughput Screen. 2024;27(12):1735-1744. doi: 10.2174/1386207326666230913105858.
6
Structure and anti-inflammatory activity of neo-clerodane diterpenoids from Scutellaria barbata.黄芩中新的裂环烯醚萜二萜类化合物的结构与抗炎活性。
Phytochemistry. 2023 Sep;213:113771. doi: 10.1016/j.phytochem.2023.113771. Epub 2023 Jun 21.
7
Identification of Flavonoids from D. Don as Inhibitors of HIV-1 and Cathepsin L Proteases and Their Structure-Activity Relationships.从 D. Don 中鉴定出作为 HIV-1 和组织蛋白酶 L 蛋白酶抑制剂的类黄酮及其构效关系。
Molecules. 2023 May 31;28(11):4476. doi: 10.3390/molecules28114476.
8
Salvigenin Suppresses Hepatocellular Carcinoma Glycolysis and Chemoresistance Through Inactivating the PI3K/AKT/GSK-3β Pathway.水飞蓟宾通过抑制 PI3K/AKT/GSK-3β 通路抑制肝癌糖酵解和化疗耐药性。
Appl Biochem Biotechnol. 2023 Aug;195(8):5217-5237. doi: 10.1007/s12010-023-04511-z. Epub 2023 May 2.
9
Study on the mechanism of action of on hepatocellular carcinoma based on network pharmacology and bioinformatics.基于网络药理学和生物信息学的[药物名称]对肝细胞癌作用机制的研究 (注:原文中“of on”之间缺少具体药物名称)
Front Pharmacol. 2023 Jan 9;13:1072547. doi: 10.3389/fphar.2022.1072547. eCollection 2022.
10
A strategy integrating parent ions list-modified mass defect filtering-diagnostic product ions for rapid screening and systematic characterization of flavonoids in Scutellaria barbata using hybrid quadrupole-orbitrap high-resolution mass spectrometry.采用混合四极杆-轨道阱高分辨质谱,通过母离子列表修饰的质量亏损过滤-诊断产物离子策略,实现对黄芩中黄酮类化合物的快速筛选和系统表征。
J Chromatogr A. 2022 Jul 5;1674:463149. doi: 10.1016/j.chroma.2022.463149. Epub 2022 May 14.