• 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

抑制 STAT3 信号通路参与了由苦参和金银花组成的中药复方的抗黑色素瘤作用。

Inhibiting STAT3 signaling is involved in the anti-melanoma effects of a herbal formula comprising Sophorae Flos and Lonicerae Japonicae Flos.

机构信息

Center for Cancer and Inflammation Research, School of Chinese Medicine, Hong Kong Baptist University, Kowloon Tong, Hong Kong, China.

Research and Development Centre for Natural Health Products, HKBU Shenzhen Research Institute and Continuing Education, Shenzhen, China.

出版信息

Sci Rep. 2017 Jun 8;7(1):3097. doi: 10.1038/s41598-017-03351-2.

DOI:10.1038/s41598-017-03351-2
PMID:28596565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5465088/
Abstract

A herbal formula (SL) comprising Sophorae Flos and Lonicerae Japonicae Flos was traditionally used to treat melanoma. Constitutively active signal transducer and activator of transcription 3 (STAT3) has been proposed as a therapeutic target in melanoma. Here we investigated whether an ethanolic extract of SL (SLE) exerted anti-melanoma activities by inhibiting STAT3 signaling. B16F10 allograft model, A375 and B16F10 cells were employed to assess the in vivo and in vitro anti-melanoma activities of SLE. A375 cells stably expressing STAT3C, a constitutively active STAT3 mutant, were used to determine the role of STAT3 signaling in SLE's anti-melanoma effects. Intragastric administration of SLE (1.2 g/kg) potently inhibited melanoma growth in mice and inhibited STAT3 phosphorylation in the tumors. In cultured cells, SLE dramatically reduced cell viability, induced apoptosis, suppressed migration and invasion, and restrained STAT3 activation and nuclear localization. STAT3C overexpression in A375 cells diminished SLE's effects on cell viability, apoptosis and invasion. Collectively, SLE exerted potent anti-melanoma effects partially by inhibiting STAT3 signaling. This study provides pharmacological justification for the traditional use of this formula in treating melanoma, and suggests that SLE has the potential to be developed as a modern alternative and/or complimentary agent for melanoma treatment and prevention.

摘要

一种包含苦参和金银花的草药配方(SL)传统上用于治疗黑色素瘤。组成性激活的信号转导和转录激活因子 3(STAT3)已被提议作为黑色素瘤的治疗靶点。在这里,我们研究了 SL 的乙醇提取物(SLE)是否通过抑制 STAT3 信号传导发挥抗黑色素瘤活性。B16F10 同种异体移植模型、A375 和 B16F10 细胞被用于评估 SLE 的体内和体外抗黑色素瘤活性。使用稳定表达组成性激活 STAT3 突变体 STAT3C 的 A375 细胞来确定 STAT3 信号在 SLE 的抗黑色素瘤作用中的作用。SLE(1.2 g/kg)的胃内给药强烈抑制了小鼠黑色素瘤的生长,并抑制了肿瘤中的 STAT3 磷酸化。在培养的细胞中,SLE 显著降低细胞活力,诱导细胞凋亡,抑制迁移和侵袭,并抑制 STAT3 激活和核定位。A375 细胞中 STAT3C 的过表达减弱了 SLE 对细胞活力、细胞凋亡和侵袭的影响。总之,SLE 通过抑制 STAT3 信号发挥强大的抗黑色素瘤作用。这项研究为该配方在治疗黑色素瘤中的传统用途提供了药理学依据,并表明 SLE 有可能被开发为治疗和预防黑色素瘤的现代替代药物和/或补充药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/19b7fdf57db3/41598_2017_3351_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/4b1a3bec1802/41598_2017_3351_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/1c2a3032eabb/41598_2017_3351_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/4b2fc56d4c78/41598_2017_3351_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/1446a74d9eef/41598_2017_3351_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/19eb54283830/41598_2017_3351_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/9d698f2e239d/41598_2017_3351_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/19b7fdf57db3/41598_2017_3351_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/4b1a3bec1802/41598_2017_3351_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/1c2a3032eabb/41598_2017_3351_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/4b2fc56d4c78/41598_2017_3351_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/1446a74d9eef/41598_2017_3351_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/19eb54283830/41598_2017_3351_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/9d698f2e239d/41598_2017_3351_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/5465088/19b7fdf57db3/41598_2017_3351_Fig7_HTML.jpg

相似文献

1
Inhibiting STAT3 signaling is involved in the anti-melanoma effects of a herbal formula comprising Sophorae Flos and Lonicerae Japonicae Flos.抑制 STAT3 信号通路参与了由苦参和金银花组成的中药复方的抗黑色素瘤作用。
Sci Rep. 2017 Jun 8;7(1):3097. doi: 10.1038/s41598-017-03351-2.
2
A TCM formula comprising Sophorae Flos and Lonicerae Japonicae Flos alters compositions of immune cells and molecules of the STAT3 pathway in melanoma microenvironment.一个包含苦参和金银花的中药配方改变了黑色素瘤微环境中免疫细胞和 STAT3 通路分子的组成。
Pharmacol Res. 2019 Apr;142:115-126. doi: 10.1016/j.phrs.2019.02.020. Epub 2019 Feb 20.
3
MiR-let-7a/f-CCR7 signaling is involved in the anti-metastatic effects of an herbal formula comprising Sophorae Flos and Lonicerae Japonicae Flos in melanoma.miR-let-7a/f-CCR7 信号通路参与了由槐米和金银花组成的中药复方在黑色素瘤中抗转移作用的机制。
Phytomedicine. 2019 Nov;64:153084. doi: 10.1016/j.phymed.2019.153084. Epub 2019 Sep 5.
4
A two-herb formula inhibits STAT3 signaling and exerts anti-melanoma effects in cell and animal models.两味草药配方可抑制 STAT3 信号传导并在细胞和动物模型中发挥抗黑色素瘤作用。
J Ethnopharmacol. 2021 Mar 25;268:113671. doi: 10.1016/j.jep.2020.113671. Epub 2020 Dec 8.
5
The JAK2/STAT3 pathway is involved in the anti-melanoma effects of brevilin A.JAK2/STAT3 通路参与了白藜芦醇 A 的抗黑色素瘤作用。
Life Sci. 2020 Jan 15;241:117169. doi: 10.1016/j.lfs.2019.117169. Epub 2019 Dec 14.
6
Quercetin exerts anti-melanoma activities and inhibits STAT3 signaling.槲皮素具有抗黑色素瘤活性,并抑制 STAT3 信号通路。
Biochem Pharmacol. 2014 Feb 1;87(3):424-34. doi: 10.1016/j.bcp.2013.11.008. Epub 2013 Nov 23.
7
Luteolin binds Src, promotes STAT3 protein ubiquitination and exerts anti-melanoma effects in cell and mouse models.木犀草素与Src结合,促进STAT3蛋白泛素化,并在细胞和小鼠模型中发挥抗黑色素瘤作用。
Biochem Pharmacol. 2022 Jun;200:115044. doi: 10.1016/j.bcp.2022.115044. Epub 2022 Apr 20.
8
Inhibition of STAT3 signaling contributes to the anti-melanoma effects of chrysoeriol.STAT3 信号抑制有助于 chrysoeriol 的抗黑色素瘤作用。
Phytomedicine. 2023 Jan;109:154572. doi: 10.1016/j.phymed.2022.154572. Epub 2022 Nov 20.
9
Pien Tze Huang inhibits tumor cell proliferation and promotes apoptosis via suppressing the STAT3 pathway in a colorectal cancer mouse model.片仔癀通过抑制结直肠癌小鼠模型中的 STAT3 通路抑制肿瘤细胞增殖并促进细胞凋亡。
Int J Oncol. 2012 May;40(5):1569-74. doi: 10.3892/ijo.2012.1326. Epub 2012 Jan 3.
10
Artesunate inhibits melanoma progression in vitro via suppressing STAT3 signaling pathway.青蒿琥酯通过抑制 STAT3 信号通路抑制体外黑素瘤的进展。
Pharmacol Rep. 2021 Apr;73(2):650-663. doi: 10.1007/s43440-021-00230-6. Epub 2021 Feb 20.

引用本文的文献

1
with the homology of medicine and food: a review of active ingredients, anticancer mechanisms, pharmacokinetics, quality control, toxicity and applications.药食同源:活性成分、抗癌机制、药代动力学、质量控制、毒性及应用综述
Front Oncol. 2024 Sep 9;14:1446328. doi: 10.3389/fonc.2024.1446328. eCollection 2024.
2
Arnicolide D: a multi-targeted anticancer sesquiterpene lactone-preclinical efficacy and mechanistic insights.莪术醇 D:一种多靶点的抗癌倍半萜内酯——临床前疗效和机制见解。
Naunyn Schmiedebergs Arch Pharmacol. 2024 Sep;397(9):6317-6336. doi: 10.1007/s00210-024-03095-7. Epub 2024 Apr 23.
3
Dexamethasone and OLT1177 Cooperate in the Reduction of Melanoma Growth by Inhibiting STAT3 Functions.

本文引用的文献

1
Icariside II overcomes TRAIL resistance of melanoma cells through ROS-mediated downregulation of STAT3/cFLIP signaling.淫羊藿苷II通过ROS介导的STAT3/cFLIP信号下调克服黑色素瘤细胞的TRAIL耐药性。
Oncotarget. 2016 Aug 9;7(32):52218-52229. doi: 10.18632/oncotarget.10582.
2
Iciartin, a novel FASN inhibitor, exerts anti-melanoma activities through IGF-1R/STAT3 signaling.Iciartin是一种新型脂肪酸合酶(FASN)抑制剂,通过胰岛素样生长因子-1受体(IGF-1R)/信号转导和转录激活因子3(STAT3)信号通路发挥抗黑色素瘤活性。
Oncotarget. 2016 Aug 9;7(32):51251-51269. doi: 10.18632/oncotarget.9984.
3
Inhibition of the STAT3 signaling pathway contributes to apigenin-mediated anti-metastatic effect in melanoma.
地塞米松和 OLT1177 通过抑制 STAT3 功能协同减少黑色素瘤生长。
Cells. 2023 Jan 12;12(2):294. doi: 10.3390/cells12020294.
4
Flos puerariae ameliorates the intestinal inflammation of modulating the Nrf2/Keap1, JAK-STAT and Wnt signaling.葛花通过调节Nrf2/Keap1、JAK-STAT和Wnt信号通路改善肠道炎症。
Front Pharmacol. 2022 Aug 17;13:893758. doi: 10.3389/fphar.2022.893758. eCollection 2022.
5
Advances in Molecular Mechanisms for Traditional Chinese Medicine Actions in Regulating Tumor Immune Responses.中药调控肿瘤免疫反应作用的分子机制研究进展
Front Pharmacol. 2020 Jul 8;11:1009. doi: 10.3389/fphar.2020.01009. eCollection 2020.
6
Activation of STAT3 is a key event in TLR4 signaling-mediated melanoma progression.STAT3 的激活是 TLR4 信号转导介导的黑色素瘤进展中的关键事件。
Cell Death Dis. 2020 Apr 20;11(4):246. doi: 10.1038/s41419-020-2440-1.
7
Inhibiting the Src/STAT3 signaling pathway contributes to the anti-melanoma mechanisms of dioscin.抑制Src/STAT3信号通路有助于薯蓣皂苷的抗黑色素瘤机制。
Oncol Lett. 2020 Mar;19(3):2508-2514. doi: 10.3892/ol.2020.11315. Epub 2020 Jan 17.
8
STAT3 and STAT5 Targeting for Simultaneous Management of Melanoma and Autoimmune Diseases.靶向 STAT3 和 STAT5 同时治疗黑色素瘤和自身免疫性疾病
Cancers (Basel). 2019 Sep 27;11(10):1448. doi: 10.3390/cancers11101448.
9
Mycelia Exert Anti-liver Cancer Effects and Inhibit STAT3 Signaling and .菌丝体发挥抗肝癌作用并抑制信号转导和转录激活因子3(STAT3)信号传导 以及 。 你提供的原文似乎不太完整,句末“and.”表述不太明确,以上是根据现有内容翻译的结果。
Front Pharmacol. 2018 Dec 17;9:1449. doi: 10.3389/fphar.2018.01449. eCollection 2018.
抑制信号转导和转录激活因子3(STAT3)信号通路有助于芹菜素介导的黑色素瘤抗转移作用。
Sci Rep. 2016 Feb 25;6:21731. doi: 10.1038/srep21731.
4
Lonicerae Japonicae Flos and Lonicerae Flos: A Systematic Pharmacology Review.金银花与忍冬花:系统药理学综述
Evid Based Complement Alternat Med. 2015;2015:905063. doi: 10.1155/2015/905063. Epub 2015 Jul 16.
5
Quercetin inhibits HGF/c-Met signaling and HGF-stimulated melanoma cell migration and invasion.槲皮素抑制HGF/c-Met信号传导以及HGF刺激的黑色素瘤细胞迁移和侵袭。
Mol Cancer. 2015 May 14;14:103. doi: 10.1186/s12943-015-0367-4.
6
Phase I study of OPB-51602, an oral inhibitor of signal transducer and activator of transcription 3, in patients with relapsed/refractory hematological malignancies.OPB-51602(一种信号转导和转录激活因子3口服抑制剂)用于复发/难治性血液系统恶性肿瘤患者的I期研究。
Cancer Sci. 2015 Jul;106(7):896-901. doi: 10.1111/cas.12683. Epub 2015 May 25.
7
The cost of ipilimumab toxicity: a single-centre analysis.伊匹单抗毒性的成本:单中心分析。
Melanoma Res. 2015 Jun;25(3):259-64. doi: 10.1097/CMR.0000000000000158.
8
Combining immunotherapy with oncogene-targeted therapy: a new road for melanoma treatment.免疫疗法与癌基因靶向疗法相结合:黑色素瘤治疗的新途径。
Front Immunol. 2015 Feb 9;6:46. doi: 10.3389/fimmu.2015.00046. eCollection 2015.
9
Phase 1 and pharmacological trial of OPB-31121, a signal transducer and activator of transcription-3 inhibitor, in patients with advanced hepatocellular carcinoma.转录信号转导子与激活子3抑制剂OPB-31121用于晚期肝细胞癌患者的1期及药理学试验
Hepatol Res. 2015 Dec;45(13):1283-91. doi: 10.1111/hepr.12504. Epub 2015 Mar 24.
10
Inhibition of STAT3 signalling contributes to the antimelanoma action of atractylenolide II.抑制信号转导和转录激活因子3(STAT3)信号传导有助于白术内酯II的抗黑色素瘤作用。
Exp Dermatol. 2014 Nov;23(11):855-7. doi: 10.1111/exd.12527.