• 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

来自[来源未提及]的黄酮类化合物紫铆素诱导口腔癌细胞凋亡并抑制Akt信号通路。

The Flavonoid Jaceosidin from Induces Apoptotic Cell Death and Inhibits the Akt Pathway in Oral Cancer Cells.

作者信息

Han Hye-Yeon, Kim Hyung Joon, Jeong Seung-Hwa, Kim Jiyeon, Jeong Sung-Hee, Kim Gyoo Cheon, Hwang Dae-Seok, Kim Uk-Kyu, Ryu Mi Heon

机构信息

Department of Oral Pathology, School of Dentistry, Research Institute for Oral Biotechnology, Pusan National University, Yangsan, Gyeongnam 50612, Republic of Korea.

Department of Oral Physiology, BK21 Plus Project and Institute of Translational Dental Sciences, School of Dentistry, Pusan National University, Yangsan, Gyeongnam 50612, Republic of Korea.

出版信息

Evid Based Complement Alternat Med. 2018 May 13;2018:5765047. doi: 10.1155/2018/5765047. eCollection 2018.

DOI:10.1155/2018/5765047
PMID:29861773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5971256/
Abstract

Jaceosidin is a single compound from the Japanese mugwort , which is used as a food and a traditional medicinal herb. extracts and flavonoid components have been shown to have antihyperglycaemic, antioxidant, and anti-inflammatory properties. Although the anticancer properties of these extracts were recently demonstrated, the related mechanisms have not been characterised. In this study, we investigated the effects of jaceosidin in oral squamous cell carcinoma (OSCC) cells and initially showed selective suppression of proliferation (IC = 82.1 M in HSC-3 cells and 97.5 M in Ca9.22 cells) and accumulation of cells at the sub-G1 stage of the cell cycle. In addition, jaceosidin increased cleavage of caspase-9 and caspase-3 in OSCC cells, although caspase-8 was not detected. In further experiments, jaceosidin downregulated Akt phosphorylation and ectopic activation of Akt blocked the antiproliferative effects of jaceosidin. Finally, we showed that jaceosidin has no effects on HaCaT normal epithelial cell viability, indicating selective chemotherapeutic potential of jaceosidin and that tumour-specific downregulation of Akt increases apoptosis and inhibits growth in OSCC cells.

摘要

紫花前胡苷是从日本艾草中提取的单一化合物,日本艾草既是一种食物,也是一种传统草药。其提取物和黄酮类成分已被证明具有降血糖、抗氧化和抗炎特性。尽管最近已证实这些提取物具有抗癌特性,但其相关机制尚未明确。在本研究中,我们研究了紫花前胡苷对口腔鳞状细胞癌(OSCC)细胞的影响,初步显示其对细胞增殖有选择性抑制作用(在HSC-3细胞中IC = 82.1μM,在Ca9.22细胞中为97.5μM),并使细胞在细胞周期的G1期前阶段积累。此外,紫花前胡苷增加了OSCC细胞中caspase-9和caspase-3的裂解,尽管未检测到caspase-8。在进一步的实验中,紫花前胡苷下调了Akt磷酸化,而异位激活Akt则阻断了紫花前胡苷的抗增殖作用。最后,我们表明紫花前胡苷对HaCaT正常上皮细胞活力没有影响,这表明紫花前胡苷具有选择性化疗潜力,并且Akt的肿瘤特异性下调会增加OSCC细胞的凋亡并抑制其生长。

相似文献

1
The Flavonoid Jaceosidin from Induces Apoptotic Cell Death and Inhibits the Akt Pathway in Oral Cancer Cells.来自[来源未提及]的黄酮类化合物紫铆素诱导口腔癌细胞凋亡并抑制Akt信号通路。
Evid Based Complement Alternat Med. 2018 May 13;2018:5765047. doi: 10.1155/2018/5765047. eCollection 2018.
2
Jaceosidin, isolated from dietary mugwort (Artemisia princeps), induces G2/M cell cycle arrest by inactivating cdc25C-cdc2 via ATM-Chk1/2 activation.从食用艾蒿(Artemisia princeps)中分离得到的杰斯西定通过激活 ATM-Chk1/2 使 cdc25C-cdc2 失活,从而诱导 G2/M 细胞周期停滞。
Food Chem Toxicol. 2013 May;55:214-21. doi: 10.1016/j.fct.2012.12.026. Epub 2012 Dec 26.
3
Jaceosidin induces apoptosis in ras-transformed human breast epithelial cells through generation of reactive oxygen species.光紫堇定通过产生活性氧诱导ras转化的人乳腺上皮细胞凋亡。
Ann N Y Acad Sci. 2007 Jan;1095:483-95. doi: 10.1196/annals.1397.052.
4
Jaceosidin induces apoptosis through Bax activation and down-regulation of Mcl-1 and c-FLIP expression in human renal carcinoma Caki cells.Jaceosidin 通过激活 Bax 以及下调 Mcl-1 和 c-FLIP 的表达诱导人肾癌细胞 Caki 细胞凋亡。
Chem Biol Interact. 2016 Dec 25;260:168-175. doi: 10.1016/j.cbi.2016.10.011. Epub 2016 Oct 8.
5
Inhibitory effect of eupatilin and jaceosidin isolated from Artemisia princeps on carrageenan-induced inflammation in mice.从朝鲜艾蒿中分离得到的灯盏乙素和雅可西定对卡拉胶诱导的小鼠炎症的抑制作用。
J Ethnopharmacol. 2009 Sep 25;125(3):497-500. doi: 10.1016/j.jep.2009.06.001. Epub 2009 Jun 6.
6
Jaceosidin, a natural flavone, promotes angiogenesis via activation of VEGFR2/FAK/PI3K/AKT/NF-κB signaling pathways in endothelial cells.橙皮苷,一种天然黄酮类化合物,通过激活血管内皮细胞中的 VEGFR2/FAK/PI3K/AKT/NF-κB 信号通路促进血管生成。
Exp Biol Med (Maywood). 2014 Oct;239(10):1325-34. doi: 10.1177/1535370214533883. Epub 2014 Jun 17.
7
Anti-tumor effects of jaceosidin on apoptosis, autophagy, and necroptosis in human glioblastoma multiforme.香叶木素对多形性胶质母细胞瘤细胞凋亡、自噬和坏死性凋亡的抗肿瘤作用
Am J Cancer Res. 2021 Oct 15;11(10):4919-4930. eCollection 2021.
8
Inhibitory effect of eupatilin and jaceosidin isolated from Artemisia princeps in IgE-induced hypersensitivity.从白头翁中分离出的灯盏乙素和紫花前胡苷对IgE诱导的超敏反应的抑制作用。
Int Immunopharmacol. 2007 Dec 15;7(13):1678-84. doi: 10.1016/j.intimp.2007.08.028. Epub 2007 Sep 25.
9
Standardized flavonoid-rich fraction of Artemisia princeps Pampanini cv. Sajabal induces apoptosis via mitochondrial pathway in human cervical cancer HeLa cells.青蒿标准化黄酮部位诱导人宫颈癌 HeLa 细胞凋亡及其作用机制的研究。
J Ethnopharmacol. 2012 May 7;141(1):460-8. doi: 10.1016/j.jep.2012.03.011. Epub 2012 Mar 18.
10
In vitro antioxidant and anti-inflammatory activities of Jaceosidin from Artemisia princeps Pampanini cv. Sajabal.来自朝鲜艾蒿栽培品种“Sajabal”的香叶木素的体外抗氧化和抗炎活性
Arch Pharm Res. 2008 Apr;31(4):429-37. doi: 10.1007/s12272-001-1175-8. Epub 2008 May 1.

引用本文的文献

1
Jaceosidin induces apoptosis and inhibits migration in AGS gastric cancer cells by regulating ROS-mediated signaling pathways.橙皮苷通过调节 ROS 介导的信号通路诱导 AGS 胃癌细胞凋亡并抑制迁移。
Redox Rep. 2024 Dec;29(1):2313366. doi: 10.1080/13510002.2024.2313366. Epub 2024 Feb 6.
2
Flavonoids as Strong Inhibitors of MAPK3: A Computational Drug Discovery Approach.黄酮类化合物作为丝裂原活化蛋白激酶3(MAPK3)的强效抑制剂:一种计算机辅助药物发现方法。
Int J Anal Chem. 2023 Apr 14;2023:8899240. doi: 10.1155/2023/8899240. eCollection 2023.
3
Natural Bioactives: Back to the Future in the Fight against Human Papillomavirus? A Narrative Review.

本文引用的文献

1
Puerarin prevents tumor necrosis factor-α-induced apoptosis of PC12 cells via activation of the PI3K/Akt signaling pathway.葛根素通过激活PI3K/Akt信号通路预防肿瘤坏死因子-α诱导的PC12细胞凋亡。
Exp Ther Med. 2017 Jul;14(1):813-818. doi: 10.3892/etm.2017.4545. Epub 2017 Jun 6.
2
Major apoptotic mechanisms and genes involved in apoptosis.参与细胞凋亡的主要凋亡机制和基因。
Tumour Biol. 2016 Jul;37(7):8471-86. doi: 10.1007/s13277-016-5035-9. Epub 2016 Apr 9.
3
Akt inhibitors in cancer treatment: The long journey from drug discovery to clinical use (Review).
天然生物活性物质:抗击人乳头瘤病毒的回归未来?一篇叙述性综述。
J Clin Med. 2022 Mar 7;11(5):1465. doi: 10.3390/jcm11051465.
4
Identification and validation of potential novel biomarkers for oral squamous cell carcinoma.口腔鳞状细胞癌潜在新型生物标志物的鉴定和验证。
Bioengineered. 2021 Dec;12(1):8845-8862. doi: 10.1080/21655979.2021.1987089.
5
Comparison of the cytotoxic effects of different fractions of and on B16/F10, PC3 and MCF7 Cells.[具体物质]不同组分对B16/F10、PC3和MCF7细胞的细胞毒性作用比较。 (注:原文中“of and ”表述不完整,缺少具体物质名称)
Res Pharm Sci. 2020 Jul 3;15(3):273-280. doi: 10.4103/1735-5362.288434. eCollection 2020 Jun.
6
The Akt pathway in oncology therapy and beyond (Review).肿瘤治疗领域中 Akt 通路的研究进展及其相关应用(综述)。
Int J Oncol. 2018 Dec;53(6):2319-2331. doi: 10.3892/ijo.2018.4597. Epub 2018 Oct 16.
Akt抑制剂在癌症治疗中的应用:从药物发现到临床应用的漫长历程(综述)
Int J Oncol. 2016 Mar;48(3):869-85. doi: 10.3892/ijo.2015.3306. Epub 2015 Dec 24.
4
Chemopreventive effects of standardized ethanol extract from the aerial parts of Artemisia princeps Pampanini cv. Sajabal via NF-κB inactivation on colitis-associated colon tumorigenesis in mice.茵陈蒿(Sajabal品种)地上部分标准化乙醇提取物通过抑制NF-κB对小鼠结肠炎相关结肠癌发生的化学预防作用。
Food Chem Toxicol. 2015 Jan;75:14-23. doi: 10.1016/j.fct.2014.11.007. Epub 2014 Nov 13.
5
Jaceosidin, a natural flavone, promotes angiogenesis via activation of VEGFR2/FAK/PI3K/AKT/NF-κB signaling pathways in endothelial cells.橙皮苷,一种天然黄酮类化合物,通过激活血管内皮细胞中的 VEGFR2/FAK/PI3K/AKT/NF-κB 信号通路促进血管生成。
Exp Biol Med (Maywood). 2014 Oct;239(10):1325-34. doi: 10.1177/1535370214533883. Epub 2014 Jun 17.
6
Cancer statistics in Korea: incidence, mortality, survival, and prevalence in 2011.韩国癌症统计数据:2011 年的发病率、死亡率、生存率和流行率。
Cancer Res Treat. 2014 Apr;46(2):109-23. doi: 10.4143/crt.2014.46.2.109. Epub 2014 Apr 22.
7
Effect on symptom control of structured information given to patients receiving chemotherapy.给予接受化疗患者结构化信息对症状控制的影响。
Eur J Oncol Nurs. 2014 Feb;18(1):78-84. doi: 10.1016/j.ejon.2013.07.006. Epub 2013 Oct 4.
8
Isoalantolactone, a sesquiterpene lactone, induces apoptosis in SGC-7901 cells via mitochondrial and phosphatidylinositol 3-kinase/Akt signaling pathways.异土木香内酯,一种倍半萜内酯,通过线粒体和磷脂酰肌醇 3-激酶/ Akt 信号通路诱导 SGC-7901 细胞凋亡。
Arch Pharm Res. 2013 Oct;36(10):1262-9. doi: 10.1007/s12272-013-0217-0. Epub 2013 Jul 24.
9
Jaceosidin, isolated from dietary mugwort (Artemisia princeps), induces G2/M cell cycle arrest by inactivating cdc25C-cdc2 via ATM-Chk1/2 activation.从食用艾蒿(Artemisia princeps)中分离得到的杰斯西定通过激活 ATM-Chk1/2 使 cdc25C-cdc2 失活,从而诱导 G2/M 细胞周期停滞。
Food Chem Toxicol. 2013 May;55:214-21. doi: 10.1016/j.fct.2012.12.026. Epub 2012 Dec 26.
10
Dracorhodin perchlorate inhibits PI3K/Akt and NF-κB activation, up-regulates the expression of p53, and enhances apoptosis.高氯酸血根碱抑制 PI3K/Akt 和 NF-κB 的激活,上调 p53 的表达,并增强细胞凋亡。
Apoptosis. 2012 Oct;17(10):1104-19. doi: 10.1007/s10495-012-0742-1.