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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.

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/12030738/0c12868b4fd5/pharmaceuticals-18-00472-g001.jpg

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