| 71 | 0 | 97 |
| 下载次数 | 被引频次 | 阅读次数 |
目的 探究天然化合物新藤黄酸对喉癌(Tu686)细胞增殖、迁移的影响及其作用机制。方法 采用MTT法、平板克隆、划痕实验、Transwell实验、Hoechst 33258染色等方法,分析新藤黄酸对Tu686细胞生长、迁移的影响。网络药理学及分子对接预测新藤黄酸作用于喉癌细胞的分子靶点,最后Western blot实验检测相关蛋白的表达水平并予以验证。结果 新藤黄酸可显著抑制Tu686细胞的增殖以及迁移、侵袭能力。网络药理学筛选获得新藤黄酸-喉癌共同靶点19个,KEGG富集分析提示,新藤黄酸可能通过调控癌症相关通路等抑制肿瘤进程。分子对接结果显示,新藤黄酸与核心靶点具有强结合活性。Hoechst 33258染色和Western blot结果表明,新藤黄酸可以诱导Tu686细胞凋亡,并且还可使STAT3、BCL2蛋白表达下调,BAX蛋白表达上调。结论 新藤黄酸对Tu686细胞的增殖、迁移能力有明显的抑制作用,并且可能与多种靶点有关。
Abstract:Objective To investigate the effect of gambogenic acid on the proliferation and migration of laryngeal cancer Tu686 cells and its mechanism.Methods The effects of gambogenic acid on the growth and migration of Tu686 cells were analyzed by MTT assay, plate cloning assay, wound healing assay, Transwell assay and Hoechst 33258 staining.The molecular targets of gambogenic acid on laryngeal cancer cells was predicted by Network pharmacology and molecular docking, and the expression levels of related proteins were detected by Western blot.Results Gambogenic acid significantly inhibited the proliferation, migration and invasion of Tu686 cells.Network pharmacology screening identified 19 common targets of gambogenic acid-laryngeal cancer.KEGG enrichment analysis suggested that gambogenic acid might inhibit tumor progression by regulating cancer-related pathways.Molecular docking results showed that gambogenic acid had strong binding activity to the core targets.Hoechst 33258 staining and Western blot results showed that gambogenic acid could induce apoptosis of Tu686,down-regulate the expression of STAT3 and BCL2 proteins and up-regulate the expression of BAX protein.Conclusion Gambogenic acid can significantly inhibit the proliferation and migration of laryngeal cancer Tu686 cells, which may be related to multiple targets.
[1]BRAY F,LAVERSANNE M,SUNG H,et al.Global cancer statistics 2022:GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J].CA Cancer J Clin,2024,74(3):229
[2]SUNG H,FERLAY J,SIEGEL R L,et al.Global cancer statistics 2020:GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J].CA Cancer J Clin,2021,71(3):209
[3]CAMPBELL G,GLAZER T A,KIMPLE R J,et al.Advances in organ preservation for laryngeal cancer[J].Curr Treat Options Oncol,2022,23(4):594
[4]熊嫣,胡逸灵,熊洁,等.藤黄属药用植物活性成分的药理作用及其机制研究新进展[J].中国野生植物资源,2024,43(6):85
[5]MI L,XING Z,ZHANG Y,et al.Unveiling gambogenic acid as a promising antitumor compound:a review[J].Planta Med,2024,90(5):353
[6]LIU C,XU J,GUO C,et al.Gambogenic acid induces endoplasmic reticulum stress in colorectal cancer via the aurora a pathway[J].Front Cell Dev Biol,2021,9:736350
[7]WU J,WANG D,ZHOU J,et al.Gambogenic acid induces apoptosis and autophagy through ROS-mediated endoplasmic reticulum stress via JNK pathway in prostate cancer cells[J].Phytother Res,2023,37(1):310
[8]ZHOU S,ZHAO N,WANG J.Gambogenic acid suppresses bladder cancer cells growth and metastasis by regulating NF-κB signaling[J].Chem Biol Drug Des,2020,96(5):1272
[9]PéREZ-GARIJO A,STELLER H.Spreading the word:non-autonomous effects of apoptosis during development,regeneration and disease[J].Development,2015,142:1183
[10]SINGH P,LIM B.Targeting apoptosis in cancer[J].Current Oncology Reports,2022,24(3):273
[11]GUHA P,GARDELL J,DARPOLOR J,et al.STAT3 inhibition induces bax-dependent apoptosis in liver tumor myeloid-derived suppressor cells[J].Oncogene,2019,38(10):1846
[12]FATHI N,RASHIDI G,KHODADADI A,et al.STAT3 and apoptosis challenges in cancer[J].Int J Biol Macromol,2018,117:993
基本信息:
DOI:10.16751/j.cnki.2095-4646.2025070815
中图分类号:R285.5
引用信息:
[1]刘艳,谢孟婷,蔡敬,等.新藤黄酸对喉癌细胞增殖、迁移的抑制作用及其机制研究[J].湖北科技学院学报(医学版),2026,40(01):6-11.DOI:10.16751/j.cnki.2095-4646.2025070815.
基金信息:
湖北科技学院五官专项(WGZX-02); 湖北省重点研发计划(大健康专项)(2022BCE011)
2026-01-20
2026-01-20