[1]要兆旭,马海滨,刘 琳,等.甘草甜素对喉癌Hep-2细胞侵袭和迁移的影响及机制研究[J].陕西医学杂志,2024,(5):604-609.[doi:DOI:10.3969/j.issn.1000-7377.2024.05.006]
 YAO Zhaoxu,MA Haibin,LIU Lin,et al.Effect of glycyrrhizin on invasion and migration of laryngeal carcinoma Hep-2 cells and its mechanism[J].,2024,(5):604-609.[doi:DOI:10.3969/j.issn.1000-7377.2024.05.006]
点击复制

甘草甜素对喉癌Hep-2细胞侵袭和迁移的影响及机制研究
分享到:

《陕西医学杂志》[ISSN:1000-7377/CN:61-1281/TN]

卷:
期数:
2024年5期
页码:
604-609
栏目:
基础研究
出版日期:
2024-05-05

文章信息/Info

Title:
Effect of glycyrrhizin on invasion and migration of laryngeal carcinoma Hep-2 cells and its mechanism
作者:
要兆旭马海滨刘 琳赵 倩巩 慧孙凯丽秦隆朝
(邯郸市中心医院耳鼻喉科,河北 邯郸 056002)
Author(s):
YAO ZhaoxuMA HaibinLIU LinZHAO QianGONG HuiSUN KailiQIN Longchao
(Department of Otolaryngology,Handan Central Hospital,Handan 056002,China)
关键词:
喉癌 Hep-2细胞 甘草甜素 微小RNA-205-5p 沉默信息调节因子2相关酶3 侵袭 迁移
Keywords:
Laryngeal cancer Hep-2 cells Glycyrrhizin microRNA-205-5p Silent mating type information regulation 2 homolog-3 Invasion Migration
分类号:
R 36
DOI:
DOI:10.3969/j.issn.1000-7377.2024.05.006
文献标志码:
A
摘要:
目的:探究甘草甜素(Gly)对喉癌Hep-2细胞侵袭和迁移的影响及作用机制。方法:体外培养正常人喉黏膜上皮细胞和喉癌Hep-2细胞,实时荧光定量PCR(RT-qPCR)法和蛋白印迹实验检测微小RNA-205-5p(miR-205-5p)、沉默信息调节因子2相关酶3(SIRT3)mRNA和蛋白表达水平。将喉癌Hep-2细胞分为对照组、Gly低浓度组、Gly中浓度组、Gly高浓度组、Gly高浓度+空载质粒组、Gly高浓度+miR-205-5p抑制剂组。各组给予相应浓度的Gly干预或转染对应质粒培养48 h。Transwell实验和划痕实验分别检测各组Hep-2细胞侵袭和迁移能力。RT-qPCR法和蛋白印迹实验检测各组Hep-2细胞miR-205-5p、SIRT3 mRNA和蛋白表达水平。双荧光素酶报告基因实验分析miR-205-5p与SIRT3的靶向关系。结果:与人喉黏膜上皮细胞比较,喉癌Hep-2细胞miR-205-5p水平降低,SIRT3 mRNA和蛋白水平升高(均P<0.05)。与对照组比较,Gly低、中、高浓度组穿膜细胞数和划痕愈合率、SIRT3 mRNA和蛋白水平依次降低,miR-205-5p水平依次升高(均P<0.05)。与Gly高浓度组和Gly高浓度+空载质粒组比较,Gly高浓度+miR-205-5p抑制剂组穿膜细胞数和划痕愈合率、SIRT3 mRNA和蛋白水平升高,miR-205-5p水平降低(均P<0.05)。miR-205-5p可靶向调控SIRT3表达。结论:Gly能够抑制Hep-2细胞侵袭和迁移,其机制可能与上调miR-205-5p表达,进而靶向下调SIRT3表达有关。
Abstract:
Objective:To explore the effect of glycyrrhizin(Gly)on invasion and migration of laryngeal carcinoma Hep-2 cells and its mechanism.Methods: Normal human laryngeal mucosal epithelial cells and laryngeal cancer Hep-2 cells were cultured in vitro,and the microRNA-205-5p(miR-205-5p),silent mating type information regulation 2 homolog-3(SIRT3)mRNA and protein levels were detected by real-time fluorescent quantitative PCR(RT-qPCR)and western blot assay.Laryngeal cancer Hep-2 cells were divided into control group,Gly low concentration group,Gly medium concentration group,Gly high concentration group,Gly high concentration+empty plasmid group,Gly high concentration+miR-205-5p inhibitor group.Each group was given Gly intervention with corresponding concentration or transfected with corresponding plasmid for 48 h.The invasion and migration ability of Hep-2 cells in each group were detected by Transwell assay and scratch assay respectively.The miR-205-5p,SIRT3 mRNA and protein levels of Hep-2 cells in each group were detected by RT-qPCR and Western blot.The targeting relationship between miR-205-5p and SIRT3 was analyzed by double luciferase reporter gene assay.Results: Compared with human laryngeal mucosal epithelial cells,the levels of miR-205-5p in laryngeal cancer Hep-2 cells were decreased,and the levels of SIRT3 mRNA and protein were increased(all P<0.05).Compared with control group,the number of transmembrane cells,scratch healing rate,SIRT3 mRNA and protein levels in Gly low,medium and high concentration groups were decreased successively,and the levels of miR-205-5p were increased successively(all P<0.05).Compared with Gly high concentration group and Gly high concentration+empty plasmid group,the number of transmembrane cells,scratch healing rate,SIRT3 mRNA and protein levels in Gly high concentration+miR-205-5p inhibitor group were increased,and the level of miR-205-5p was decreased(all P<0.05).miR-205-5p could target the regulation of SIRT3 expression.Conclusion:Gly can inhibit the invasion and migration of Hep-2 cells,and the mechanism may be related to the up-regulation of miR-205-5p expression and the targeted down-regulation of SIRT3 expression.

参考文献/References:

[1] 郭武辉,袁倩.早期喉癌患者血清膜联蛋白A2、环氧合酶-2及色素框同源物7检测及意义[J].陕西医学杂志,2021,50(11):1446-1448.
[2] 李林霏,毛福英,李斯琦,等.甘草甜素的药理活性、作用机制及其应用进展[J].中华中医药学刊,2022,40(1):242-247.
[3] SONG J,KIM J Y,YOU G,et al.Formulation of glycyrrhizic acid-based nanocomplexes for enhanced anti-cancer and anti-inflammatory effects of curcumin[J].Biotechnol Bioprocess Eng,2022,27(2):163-170.
[4] HUANG B,DING J,GUO H,et al.SIRT3 regulates the ROS-FPR1/HIF-1α axis under hypoxic conditions to influence lung cancer progression[J].Cell Biochem Biophys,2023,81(4):813-821.
[5] 赵江,唐晓龙,朱惠军.加味补中益气汤联合DOX化疗方案治疗胃癌疗效研究[J].陕西中医,2023,44(11):1554-1557.
[6] LI J,CAO X,CHU T,et al.The circHMGCS1-miR-205-5p-ErBB3 axis mediated the sanggenon C-induced anti-proliferation effects on human prostate cancer[J].Pharmacol Res,2023,187:106584.
[7] WANG L,WENG W,YANG S,et al.Circle RNA circ-0007331 promotes colorectal carcinoma by targeting miR-205-5p/high-mobility group A2 axis[J].Bioengineered,2022,13(4):9312-9321.
[8] YANG W,TAN S,YANG L,et al.Exosomal miR-205-5p enhances angiogenesis and nasopharyngeal carcinoma metastasis by targeting desmocollin-2[J].Mol Ther Oncolytics,2022,24(1):612-623.
[9] ZHAO Y L,ZHANG J X,YANG J J,et al.MiR-205-5p promotes lung cancer progression and is valuable for the diagnosis of lung cancer[J].Thorac Cancer,2022,13(6):832-843.
[10] ZUO Z,HE L,DUAN X,et al.Glycyrrhizic acid exhibits strong anticancer activity in colorectal cancer cells via SIRT3 inhibition[J].Bioengineered,2022,13(2):2720-2731.
[11] QIONG H,HAN L,ZHANG N,et al.Glycyrrhizin improves the pathogenesis of psoriasis partially through IL-17A and the SIRT1-STAT3 axis[J].BMC Immunol,2021,22(1):34-44.
[12] 冯儒学,蔡仁刚,解丹丹.甘草甜素对人舌癌Cal-27细胞增殖、凋亡及侵袭能力的影响[J].现代医学,2020,48(6):747-751.
[13] 乔冰冰,庞世杰,王海叶.丹参酮ⅡA对人喉癌Hep-2细胞增殖和细胞周期的影响及机制研究[J].陕西医学杂志,2023,52(8):960-964.
[14] LUO Y,LI J,WANG B,et al.Protective effect of glycyrrhizin on osteoarthritis cartilage degeneration and inflammation response in a rat model[J].J Bioenerg Biomembr,2021,53(3):285-293.
[15] 梁奡晟雄,周红光.温滋解毒法治疗恶性肿瘤理论探讨[J].陕西中医,2023,44(7):913-916.
[16] DANG X L,YANG L F,SHI L,et al.Post-treatment with glycyrrhizin can attenuate hepatic mitochondrial damage induced by acetaminophen in mice[J].Exp Biol Med(Maywood),2021,246(10):1219-1227.
[17] POUSTFOROOSH A,FARAMARZ S,NEGAHDARIPOUR M,et al.Tracing the pathways and mechanisms involved in the anti-breast cancer activity of glycyrrhizin using bioinformatics tools and computational methods[J].J Biomol Struct Dyn,2023,12(1):1-15.
[18] AHMAD A,TIWARI R K,SAEED M,et al.Glycyrrhizin mediates downregulation of notch pathway resulting in initiation of apoptosis and disruption in the cell cycle progression in cervical cancer cells[J].Nutr Cancer,2022,74(2):622-639.
[19] LIU G,YANG Z F,SUN J,et al.The LINC00152/miR-205-5p/CXCL11 axis in hepatocellular carcinoma cancer-associated fibroblasts affects cancer cell phenotypes and tumor growth[J].Cell Oncol(Dordr),2022,45(6):1435-1449.
[20] TORO A U,SHUKLA S K,BANSAL P.Micronome revealed miR-205-5p as key regulator of VEGFA during cancer related angiogenesis in hepatocellular carcinoma[J].Mol Biotechnol,2023,65(7):1178-1186.
[21] HUANG W,ZENG Z,XU Y,et al.Investigating whether exosomal miR-205-5p derived from tongue squamous cell carcinoma cells stimulates the angiogenic activity of HUVECs by targeting AMOT[J].Cancer Biomark,2023,38(2):215-224.
[22] LIAO J,CHEN Z,LUO X,et al.Has-circ-0006692 promotes lung cancer progression via miR-205-5p/CDK19 axis[J].Genes(Basel),2022,13(5):846-863.
[23] LIU C,LI Y.Has-circ-0000078 regulates miR-205-5p/EREG pathway to inhibit cervical cancer progression[J].Mol Biotechnol,2023,65(9):1453-1464.
[24] SAWANT-DESSAI A,DOMINGUEZ M P,CHEN U I,et al.Transcriptional repression of SIRT3 potentiates mitochondrial aconitase activation to drive aggressive prostate cancer to the bone[J].Cancer Res,2021,81(1):50-63.
[25] ZHEN L,PAN W.ALKBH5 inhibits the SIRT3/ACC1 axis to regulate fatty acid metabolism via an m6A-IGF2BP1-dependent manner in cervical squamous cell carcinoma[J].Clin Exp Pharmacol Physiol,2023,50(5):380-392.

相似文献/References:

[1]郭武辉,袁 倩.早期喉癌患者血清膜联蛋白A2、环氧合酶-2及色素框同源物7检测及意义[J].陕西医学杂志,2021,50(11):1446.[doi:DOI:10.3969/j.issn.1000-7377.2021.11.031]

备注/Memo

备注/Memo:
基金项目:河北省医学科学研究课题(20230468)
更新日期/Last Update: 2024-05-06