• 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

紫草素的结构与抗妇科恶性肿瘤研究进展

Research Progress on Structure and Anti-Gynecological Malignant Tumor of Shikonin.

作者信息

Ke Li-Na, Kong Ling-Qi, Xu Huan-Huan, Chen Qin-Hua, Dong Yun, Li Bin, Zeng Xiao-Hua, Wang Hong-Mei

机构信息

Sinopharm Dongfeng General Hospital, Hubei University of Medicine, Shiyan, China.

Hubei Key Laboratory of Wudang Local Chinese Medicine Research, School of Pharmaceutical Sciences, Hubei University of Medicine, Shiyan, China.

出版信息

Front Chem. 2022 Jul 8;10:935894. doi: 10.3389/fchem.2022.935894. eCollection 2022.

DOI:10.3389/fchem.2022.935894
PMID:35873044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9304652/
Abstract

Gynecological malignancy seriously threatens the physical and mental health of women. Shikonin is a naphthoquinone compound with a variety of biological activities. Studies have shown that shikonin can inhibit cell proliferation, promote cell apoptosis and induce cell necrosis. And in recent years, shikonin are also being increasingly used for the study of gynecological malignant diseases. Therefore, we reviewed the mechanism of action and structure optimization of shikonin in gynecological malignant tumors, in order to provide some reference for further research and development of related drug.

摘要

妇科恶性肿瘤严重威胁着女性的身心健康。紫草素是一种具有多种生物活性的萘醌类化合物。研究表明,紫草素可抑制细胞增殖、促进细胞凋亡并诱导细胞坏死。近年来,紫草素也越来越多地用于妇科恶性疾病的研究。因此,我们综述了紫草素在妇科恶性肿瘤中的作用机制及结构优化,以期为相关药物的进一步研发提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/b8b4287eeba5/fchem-10-935894-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/bcfe2bfae1cc/fchem-10-935894-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/3b2a0323f4d1/fchem-10-935894-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/a094506c92b7/fchem-10-935894-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/9a4c271524ba/fchem-10-935894-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/b8b4287eeba5/fchem-10-935894-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/bcfe2bfae1cc/fchem-10-935894-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/3b2a0323f4d1/fchem-10-935894-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/a094506c92b7/fchem-10-935894-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/9a4c271524ba/fchem-10-935894-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e97/9304652/b8b4287eeba5/fchem-10-935894-g005.jpg

相似文献

1
Research Progress on Structure and Anti-Gynecological Malignant Tumor of Shikonin.紫草素的结构与抗妇科恶性肿瘤研究进展
Front Chem. 2022 Jul 8;10:935894. doi: 10.3389/fchem.2022.935894. eCollection 2022.
2
TRAIL Enhances Shikonin Induced Apoptosis through ROS/JNK Signaling in Cholangiocarcinoma Cells.TRAIL通过ROS/JNK信号通路增强紫草素诱导的胆管癌细胞凋亡。
Cell Physiol Biochem. 2017;42(3):1073-1086. doi: 10.1159/000478758. Epub 2017 Jun 29.
3
Shikonin inhibits TNF-α-induced growth and invasion of rat aortic vascular smooth muscle cells.紫草素抑制肿瘤坏死因子-α诱导的大鼠主动脉血管平滑肌细胞的生长和侵袭。
Can J Physiol Pharmacol. 2015 Aug;93(8):615-24. doi: 10.1139/cjpp-2014-0464. Epub 2015 Mar 18.
4
Shikonin exerts antitumor activity in Burkitt's lymphoma by inhibiting C-MYC and PI3K/AKT/mTOR pathway and acts synergistically with doxorubicin.紫草素通过抑制 C-MYC 和 PI3K/AKT/mTOR 通路发挥抗伯基特淋巴瘤活性,并与阿霉素具有协同作用。
Sci Rep. 2018 Feb 20;8(1):3317. doi: 10.1038/s41598-018-21570-z.
5
Shikonin, a Chinese plant-derived naphthoquinone, induces apoptosis in hepatocellular carcinoma cells through reactive oxygen species: A potential new treatment for hepatocellular carcinoma.紫草素,一种源自中国植物的萘醌,通过活性氧诱导肝癌细胞凋亡:肝癌治疗的新方法。
Free Radic Biol Med. 2011 Dec 15;51(12):2259-71. doi: 10.1016/j.freeradbiomed.2011.09.018. Epub 2011 Sep 22.
6
Shikonin induces ROS-based mitochondria-mediated apoptosis in colon cancer.紫草素诱导结肠癌中基于活性氧的线粒体介导的细胞凋亡。
Oncotarget. 2017 Nov 17;8(65):109094-109106. doi: 10.18632/oncotarget.22618. eCollection 2017 Dec 12.
7
Inhibition of the STAT3 Signaling Pathway Contributes to the Anti-Melanoma Activities of Shikonin.抑制STAT3信号通路有助于紫草素的抗黑色素瘤活性。
Front Pharmacol. 2020 May 27;11:748. doi: 10.3389/fphar.2020.00748. eCollection 2020.
8
Shikonin induced Apoptosis Mediated by Endoplasmic Reticulum Stress in Colorectal Cancer Cells.紫草素通过内质网应激介导的细胞凋亡作用于结肠癌细胞。
J Cancer. 2022 Jan 1;13(1):243-252. doi: 10.7150/jca.65297. eCollection 2022.
9
Cbl participates in shikonin-induced apoptosis by negatively regulating phosphoinositide 3-kinase/protein kinase B signaling.Cbl通过负向调节磷酸肌醇3激酶/蛋白激酶B信号传导参与紫草素诱导的细胞凋亡。
Mol Med Rep. 2015 Jul;12(1):1305-13. doi: 10.3892/mmr.2015.3510. Epub 2015 Mar 18.
10
Anti-cancer Research on Arnebiae radix-derived Naphthoquinone in Recent Five Years.近五年来瑞香狼毒根萘醌类化合物的抗癌研究
Recent Pat Anticancer Drug Discov. 2022;17(3):218-230. doi: 10.2174/1574892816666211209164745.

引用本文的文献

1
Review projecting shikonin as a therapeutic candidate in female carcinomas: a preclinical perspective.展望紫草素作为女性癌症治疗候选药物:临床前视角
Front Pharmacol. 2025 Jul 4;16:1627124. doi: 10.3389/fphar.2025.1627124. eCollection 2025.
2
Shikonin inhibits epithelial-mesenchymal transition in glioblastoma cells by upregulating p53 and promoting miR-361-5p level to suppress ZEB1 expression.紫草素通过上调p53和提高miR-361-5p水平以抑制锌指蛋白E盒结合因子1(ZEB1)的表达,从而抑制胶质母细胞瘤细胞的上皮-间质转化。
BMC Neurosci. 2025 Jul 1;26(1):37. doi: 10.1186/s12868-025-00956-6.
3
The Identification of a Key Regulator of Mitochondrial Metabolism, the LRPPRC Protein, as a Novel Therapeutic Target in SDHA-Overexpressing Ovarian Tumors.

本文引用的文献

1
Differential relieving effects of shikonin and its derivatives on inflammation and mucosal barrier damage caused by ulcerative colitis.紫草素及其衍生物对溃疡性结肠炎所致炎症和黏膜屏障损伤的差异缓解作用。
PeerJ. 2021 Jan 7;9:e10675. doi: 10.7717/peerj.10675. eCollection 2021.
2
Biosynthesis of Novel Shikonin Glucosides by Enzymatic Glycosylation.通过酶促糖基化生物合成新型紫草素糖苷
Chem Pharm Bull (Tokyo). 2019;67(10):1072-1075. doi: 10.1248/cpb.c19-00284.
3
Pharmacological properties and derivatives of shikonin-A review in recent years.
线粒体代谢关键调节因子LRPPRC蛋白被鉴定为SDHA过表达卵巢肿瘤的新型治疗靶点。
Cancers (Basel). 2025 Jun 11;17(12):1942. doi: 10.3390/cancers17121942.
4
Integration of active ingredients from traditional Chinese medicine with nano-delivery systems for tumor immunotherapy.中药活性成分与纳米递送系统整合用于肿瘤免疫治疗
J Nanobiotechnology. 2025 May 17;23(1):357. doi: 10.1186/s12951-025-03378-y.
5
Upregulation of Succinate Dehydrogenase (SDHA) Contributes to Enhanced Bioenergetics of Ovarian Cancer Cells and Higher Sensitivity to Anti-Metabolic Agent Shikonin.琥珀酸脱氢酶(SDHA)的上调有助于增强卵巢癌细胞的生物能量代谢,并提高其对抗代谢药物紫草素的敏感性。
Cancers (Basel). 2022 Oct 18;14(20):5097. doi: 10.3390/cancers14205097.
近年来紫草素-A 的药理学性质和衍生物研究进展综述。
Pharmacol Res. 2019 Nov;149:104463. doi: 10.1016/j.phrs.2019.104463. Epub 2019 Sep 22.
4
Discovery and synthesis of sulfur-containing 6-substituted 5,8-dimethoxy-1,4-naphthoquinone oxime derivatives as new and potential anti-MDR cancer agents.发现并合成含硫的 6-取代 5,8-二甲氧基-1,4-萘醌肟衍生物,作为新型有潜力的抗多药耐药性癌症药物。
Eur J Med Chem. 2019 Mar 1;165:160-171. doi: 10.1016/j.ejmech.2019.01.005. Epub 2019 Jan 10.
5
Shikonin induces mitochondria-mediated apoptosis and attenuates epithelial-mesenchymal transition in cisplatin-resistant human ovarian cancer cells.紫草素诱导顺铂耐药的人卵巢癌细胞发生线粒体介导的凋亡并减弱上皮-间质转化。
Oncol Lett. 2018 Apr;15(4):5417-5424. doi: 10.3892/ol.2018.8065. Epub 2018 Feb 15.
6
Targeting Cell Necroptosis and Apoptosis Induced by Shikonin via Receptor Interacting Protein Kinases in Estrogen Receptor Positive Breast Cancer Cell Line, MCF-7.通过受体相互作用蛋白激酶靶向紫草素诱导雌激素受体阳性乳腺癌细胞系MCF-7中的细胞坏死性凋亡和凋亡
Anticancer Agents Med Chem. 2018;18(2):245-254. doi: 10.2174/1871520617666170919164055.
7
Salidroside Suppresses HUVECs Cell Injury Induced by Oxidative Stress through Activating the Nrf2 Signaling Pathway.红景天苷通过激活Nrf2信号通路抑制氧化应激诱导的人脐静脉内皮细胞损伤。
Molecules. 2016 Aug 9;21(8):1033. doi: 10.3390/molecules21081033.
8
Estrogen receptor alpha and beta in health and disease.健康与疾病中的雌激素受体α和β
Best Pract Res Clin Endocrinol Metab. 2015 Aug;29(4):557-68. doi: 10.1016/j.beem.2015.04.008. Epub 2015 Apr 26.
9
Inhibition of STAT3, FAK and Src mediated signaling reduces cancer stem cell load, tumorigenic potential and metastasis in breast cancer.抑制STAT3、粘着斑激酶(FAK)和Src介导的信号传导可降低乳腺癌中癌症干细胞的数量、致瘤潜力和转移能力。
Sci Rep. 2015 May 14;5:10194. doi: 10.1038/srep10194.
10
[Beta-HIVS combined cisplatin inhibited activities of human ovarian cancer cell line SKOV3 in vitro].β-人免疫缺陷病毒与顺铂联合使用在体外抑制人卵巢癌细胞系SKOV3的活性
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2014 Aug;34(8):987-90.