• 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

丹皮酚通过凋亡途径抑制膀胱癌进展:来自体外和体内研究的见解

Paeonol Suppresses Bladder Cancer Progression via Apoptotic Pathways: Insights from In Vitro and In Vivo Studies.

作者信息

Ying Lu, Chen Ruolan, Guo Rui, Liang Youfeng, Hao Mingxuan, Chen Xiaoyang, Zhang Wenjing, Yu Changyuan, Yang Zhao

机构信息

College of Life Science and Technology, Innovation Center of Molecular Diagnostics, Beijing University of Chemical Technology, Beijing 100029, China.

College of Life Science and Technology, State Key Laboratory Incubation Base for Conservation and Utilization of Bio-Resource in Tarim Basin, Tarim University, Alar 843300, China.

出版信息

Pharmaceuticals (Basel). 2025 Mar 27;18(4):472. doi: 10.3390/ph18040472.

DOI:10.3390/ph18040472
PMID:40283909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12030738/
Abstract

: Bladder cancer (BC), a highly heterogeneous and mutation-prone malignancy, remains a significant therapeutic challenge due to its propensity for recurrence, metastasis, and drug resistance. Natural products, particularly paeonol, a bioactive compound derived from Moutan Cortex in traditional Chinese medicine, have shown promising potential in cancer therapy. This study aims to evaluate the anti-BC effects of paeonol and elucidate its underlying molecular mechanisms. : In vitro experiments were conducted using T24 and J82 BC cell lines to assess paeonol's effects on cell viability, migration, apoptosis, and cell cycle progression via CCK-8, scratch, flow cytometry, RT-qPCR, and Western blot analyses. In vivo efficacy was evaluated using a xenograft mouse model, with tumor growth monitored and histopathological analysis performed. : Paeonol significantly inhibited BC cell proliferation and migration in a dose- and time-dependent manner, with IC values of 225 μg/mL (T24) and 124 μg/mL (J82) at 48 h. It induced apoptosis and arrested the cell cycle at the G1 phase, accompanied by upregulation of pro-apoptotic proteins (BID, BAX, BIM, and p53). In vivo, paeonol reduced tumor volume and weight without histopathological abnormalities in vital organs. : Paeonol exhibits potent anti-BC activity by apoptotic pathways and by arresting the cell cycle at the G1 phase and inhibiting tumor growth. Its favorable safety profile and multi-target mechanisms highlight its potential as a promising therapeutic candidate for BC. These findings provide a foundation for further clinical development of paeonol-based therapies.

摘要

膀胱癌(BC)是一种高度异质性且易于发生突变的恶性肿瘤,由于其具有复发、转移和耐药性的倾向,仍然是一个重大的治疗挑战。天然产物,特别是丹皮酚,一种源自中药牡丹皮的生物活性化合物,在癌症治疗中显示出有前景的潜力。本研究旨在评估丹皮酚的抗膀胱癌作用并阐明其潜在的分子机制。:使用T24和J82膀胱癌细胞系进行体外实验,通过CCK-8、划痕、流式细胞术、RT-qPCR和蛋白质免疫印迹分析来评估丹皮酚对细胞活力、迁移、凋亡和细胞周期进程的影响。使用异种移植小鼠模型评估体内疗效,监测肿瘤生长并进行组织病理学分析。:丹皮酚以剂量和时间依赖性方式显著抑制膀胱癌细胞增殖和迁移,在48小时时,T24细胞系的IC值为225μg/mL,J82细胞系的IC值为124μg/mL。它诱导细胞凋亡并使细胞周期停滞在G1期,同时促凋亡蛋白(BID、BAX、BIM和p53)上调。在体内,丹皮酚减小了肿瘤体积和重量,重要器官无组织病理学异常。:丹皮酚通过凋亡途径、使细胞周期停滞在G1期以及抑制肿瘤生长表现出强大的抗膀胱癌活性。其良好的安全性和多靶点作用机制突出了它作为膀胱癌有前景的治疗候选药物的潜力。这些发现为基于丹皮酚的疗法的进一步临床开发奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/e2e4bdb6e882/pharmaceuticals-18-00472-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/0c12868b4fd5/pharmaceuticals-18-00472-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/c307f693f48a/pharmaceuticals-18-00472-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/f09ef335c69c/pharmaceuticals-18-00472-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/e2141d30541b/pharmaceuticals-18-00472-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/cd0082252b53/pharmaceuticals-18-00472-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/1e663147885b/pharmaceuticals-18-00472-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/b5eca9ff86f5/pharmaceuticals-18-00472-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/e2e4bdb6e882/pharmaceuticals-18-00472-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/0c12868b4fd5/pharmaceuticals-18-00472-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/c307f693f48a/pharmaceuticals-18-00472-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/f09ef335c69c/pharmaceuticals-18-00472-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/e2141d30541b/pharmaceuticals-18-00472-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/cd0082252b53/pharmaceuticals-18-00472-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/1e663147885b/pharmaceuticals-18-00472-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/b5eca9ff86f5/pharmaceuticals-18-00472-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2b/12030738/e2e4bdb6e882/pharmaceuticals-18-00472-g008.jpg

相似文献

1
Paeonol Suppresses Bladder Cancer Progression via Apoptotic Pathways: Insights from In Vitro and In Vivo Studies.丹皮酚通过凋亡途径抑制膀胱癌进展:来自体外和体内研究的见解
Pharmaceuticals (Basel). 2025 Mar 27;18(4):472. doi: 10.3390/ph18040472.
2
Paeonol inhibits proliferation and induces cell apoptosis of human T24 and 5637 bladder cancer cells in vitro and in vivo.丹皮酚抑制人膀胱癌 T24 和 5637 细胞的体外和体内增殖并诱导其凋亡。
Clin Transl Oncol. 2021 Mar;23(3):601-611. doi: 10.1007/s12094-020-02455-y. Epub 2020 Jul 20.
3
Paeonol impacts ovarian cancer cell proliferation, migration, invasion and apoptosis via modulating the transforming growth factor beta/smad3 signaling pathway.丹皮酚通过调节转化生长因子β/ Smad3 信号通路影响卵巢癌细胞增殖、迁移、侵袭和凋亡。
J Physiol Pharmacol. 2023 Dec;74(6). doi: 10.26402/jpp.2023.6.06. Epub 2024 Feb 7.
4
Paeonol exerts anti‑tumor activity against colorectal cancer cells by inducing G0/G1 phase arrest and cell apoptosis via inhibiting the Wnt/β‑catenin signaling pathway.丹皮酚通过抑制 Wnt/β-连环蛋白信号通路诱导 G0/G1 期阻滞和细胞凋亡来发挥抗结直肠癌细胞的活性。
Int J Mol Med. 2020 Aug;46(2):675-684. doi: 10.3892/ijmm.2020.4629. Epub 2020 Jun 4.
5
Medicarpin induces G1 arrest and mitochondria-mediated intrinsic apoptotic pathway in bladder cancer cells.杨梅素诱导膀胱癌细胞 G1 期阻滞和线粒体介导的内在凋亡途径。
Acta Pharm. 2023 Jun 12;73(2):211-225. doi: 10.2478/acph-2023-0016. Print 2023 Jun 1.
6
Pharmacological effects and mechanisms of paeonol on antitumor and prevention of side effects of cancer therapy.丹皮酚在抗肿瘤及预防癌症治疗副作用方面的药理作用及机制。
Front Pharmacol. 2023 Jun 20;14:1194861. doi: 10.3389/fphar.2023.1194861. eCollection 2023.
7
Paeonol Inhibits Cell Proliferation, Migration and Invasion and Induces Apoptosis in Hepatocellular Carcinoma by Regulating miR-21-5p/KLF6 Axis.丹皮酚通过调控miR-21-5p/KLF6轴抑制肝癌细胞增殖、迁移和侵袭并诱导其凋亡。
Cancer Manag Res. 2020 Jul 17;12:5931-5943. doi: 10.2147/CMAR.S254485. eCollection 2020.
8
Paeonol inhibits tumor growth in gastric cancer in vitro and in vivo.丹皮酚在体外和体内均能抑制胃癌的生长。
World J Gastroenterol. 2010 Sep 21;16(35):4483-90. doi: 10.3748/wjg.v16.i35.4483.
9
AURKB promotes bladder cancer progression by deregulating the p53 DNA damage response pathway via MAD2L2.AURKB 通过 MAD2L2 来调控 p53 DNA 损伤反应通路从而促进膀胱癌的进展。
J Transl Med. 2024 Mar 21;22(1):295. doi: 10.1186/s12967-024-05099-6.
10
Paeonol Suppresses Proliferation and Motility of Non-Small-Cell Lung Cancer Cells by Disrupting STAT3/NF-κB Signaling.丹皮酚通过破坏STAT3/NF-κB信号通路抑制非小细胞肺癌细胞的增殖和运动能力。
Front Pharmacol. 2020 Nov 12;11:572616. doi: 10.3389/fphar.2020.572616. eCollection 2020.

本文引用的文献

1
Multiscale drug screening for cardiac fibrosis identifies MD2 as a therapeutic target.用于心脏纤维化的多尺度药物筛选确定MD2为治疗靶点。
Cell. 2024 Dec 12;187(25):7143-7163.e22. doi: 10.1016/j.cell.2024.09.034. Epub 2024 Oct 15.
2
Artemisinins ameliorate polycystic ovarian syndrome by mediating LONP1-CYP11A1 interaction.青蒿素通过调节 LONP1-CYP11A1 相互作用改善多囊卵巢综合征。
Science. 2024 Jun 14;384(6701):eadk5382. doi: 10.1126/science.adk5382.
3
DNA damage induces p53-independent apoptosis through ribosome stalling.DNA 损伤通过核糖体停滞诱导 p53 非依赖性细胞凋亡。
Science. 2024 May 17;384(6697):785-792. doi: 10.1126/science.adh7950. Epub 2024 May 16.
4
Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.2022 年全球癌症统计数据:全球 185 个国家和地区 36 种癌症的发病率和死亡率全球估计数。
CA Cancer J Clin. 2024 May-Jun;74(3):229-263. doi: 10.3322/caac.21834. Epub 2024 Apr 4.
5
Advances in diagnosis and treatment of bladder cancer.膀胱癌的诊断与治疗进展。
BMJ. 2024 Feb 12;384:e076743. doi: 10.1136/bmj-2023-076743.
6
The tumor-enriched small molecule gambogic amide suppresses glioma by targeting WDR1-dependent cytoskeleton remodeling.富瘤小分子藤黄酰胺通过靶向 WDR1 依赖性细胞骨架重构抑制神经胶质瘤。
Signal Transduct Target Ther. 2023 Nov 8;8(1):424. doi: 10.1038/s41392-023-01666-3.
7
Protective mechanism of Paeonol on central nervous system.丹皮酚对中枢神经系统的保护作用。
Phytother Res. 2024 Feb;38(2):470-488. doi: 10.1002/ptr.8049. Epub 2023 Oct 23.
8
Paeonol repurposing for cancer therapy: From mechanism to clinical translation.将芍药醇重新用于癌症治疗:从机制到临床转化。
Biomed Pharmacother. 2023 Sep;165:115277. doi: 10.1016/j.biopha.2023.115277. Epub 2023 Aug 4.
9
Pharmacological effects and mechanisms of paeonol on antitumor and prevention of side effects of cancer therapy.丹皮酚在抗肿瘤及预防癌症治疗副作用方面的药理作用及机制。
Front Pharmacol. 2023 Jun 20;14:1194861. doi: 10.3389/fphar.2023.1194861. eCollection 2023.
10
Targeting p53 pathways: mechanisms, structures, and advances in therapy.靶向 p53 通路:机制、结构和治疗进展。
Signal Transduct Target Ther. 2023 Mar 1;8(1):92. doi: 10.1038/s41392-023-01347-1.