[1]乔晋宇,付思雨,陈明雪,等.二甲双胍联合热疗诱导U937细胞凋亡及其机制研究[J].南京师大学报(自然科学版),2024,(03):87-96.[doi:10.3969/j.issn.1001-4616.2024.03.011]
 Qiao Jinyu,Fu Siyu,Chen Mingxue,et al.Metformin Combined with Hyperthermia Induces Apoptosis in U937 Cells and Its Mechanisms[J].Journal of Nanjing Normal University(Natural Science Edition),2024,(03):87-96.[doi:10.3969/j.issn.1001-4616.2024.03.011]
点击复制

二甲双胍联合热疗诱导U937细胞凋亡及其机制研究()
分享到:

《南京师大学报(自然科学版)》[ISSN:1001-4616/CN:32-1239/N]

卷:
期数:
2024年03期
页码:
87-96
栏目:
生物学
出版日期:
2024-09-15

文章信息/Info

Title:
Metformin Combined with Hyperthermia Induces Apoptosis in U937 Cells and Its Mechanisms
文章编号:
1001-4616(2024)03-0087-10
作者:
乔晋宇1付思雨1陈明雪1贾子贤1于大永2史丽颖1
(1.大连大学生命健康学院,辽宁 大连 116622)
(2.承德医学院基础医学院,河北 承德 067000)
Author(s):
Qiao Jinyu1Fu Siyu1Chen Mingxue1Jia Zixian1Yu Dayong2Shi Liying1
(1.School of Life and Health,Dalian University,Dalian 116622,China)
(2.School of Basic Medicine,Chengde Medical College,Chengde 067000,China)
关键词:
二甲双胍热疗细胞凋亡P38 MAPK 信号通路
Keywords:
metforminhyperthermiaapoptosisP38 MAPK signal pathway
分类号:
R733.7
DOI:
10.3969/j.issn.1001-4616.2024.03.011
文献标志码:
A
摘要:
探讨二甲双胍(Met)联合热疗(HT)诱导人白血病U937细胞凋亡及其可能的作用机制. MTT法检测二甲双胍联合温热(HT+Met)处理对U937细胞增殖的影响; Hoechst 33342染色观察U937细胞形态变化; 流式细胞术检测U937细胞凋亡、周期、活性氧以及线粒体膜电位的变化情况; Western Blot检测U937细胞中凋亡相关蛋白的表达情况. 通过细胞计数及活力实验确定Met 10 mmol/L和HT 44 ℃、15 min为化疗联合热疗的实验条件. Hoechst 33342荧光染色及Annexin V-FITC/PI流式细胞术分析表明,与Met或HT单独处理相比,HT+Met诱导U937细胞凋亡作用增强、活性氧(ROS)产生增加、线粒体膜电位(MMP)降低及G2/M期阻滞. Western Blot结果表明,与Met或HT单独处理相比,HT+Met组Bax/Bcl-2蛋白表达上调,Caspase-3和Caspase-8蛋白表达下调,周期蛋白依赖性激酶CDK1和周期蛋白Cyclin B1表达下调,p-P38/P38水平显著升高,加入NAC(一种ROS清除剂)后可显著恢复HT+Met组诱导的p-P38蛋白和Caspase-3蛋白表达. 二甲双胍联合热疗能够诱导U937细胞凋亡,其可能的作用机制为通过死亡受体(外源性)途径、ROS介导调节线粒体(内源性)途径以及P38 MAPK信号通路诱导人白血病U937细胞凋亡.
Abstract:
To investigate the induction of apoptosis in human leukemia U937 cells by metformin(Met)combined with hyperthermia(HT)and its possible mechanism of action. MTT assay was used to detect the effect of metformin combined with warm(HT+Met)treatment on the proliferation of U937 cells. Hoechst 33342 staining was used to observe the morphological changes of U937 cells. Flow cytometry was used to detect the changes of apoptosis,cycle,reactive oxygen species,and mitochondrial membrane potential in U937 cells,and Western Blot assay was used to detect the expression of apoptosis-related proteins in U937 cells. The expression of apoptosis-related proteins in U937 cells was detected by Western Blot. The cell counting and viability assays determined that Met 10 mmol/L and HT 44 ℃ for 15 min were the experimental conditions for the combination of chemotherapy and hyperthermia. Hoechst 33342 fluorescence staining and Annexin V-FITC/PI flow cytometry analysis showed that HT+Met induced enhanced apoptosis,increased reactive oxygen species(ROS)production,and mitochondrial membrane potential in U937 cells,as compared with Met or HT treatment alone. ROS production was increased,mitochondrial membrane potential(MMP)was decreased,and G2/M phase was blocked. Western Blot showed that Bax/Bcl-2 protein expression was up-regulated,Caspase-3 and Caspase-8 protein expression was down-regulated,CDK1 and Cyclin B1 expression was down-regulated in HT+Met compared with Met or HT alone,p-P38/P38 flow cytometry analysis showed that HT+Met induced apoptosis in U937 cells. The expression of Caspase-3 and Caspase-8,CDK1 and Cyclin B1 was down-regulated. The level of p-P38/P38 was significantly elevated,and the addition of NAC,a ROS scavenger,significantly restored the HT+Met-induced expression of p-P38 and Caspase-3 proteins. Metformin combined with hyperthermia induced apoptosis in U937 cells,and its possible mechanism of action is to induce cell death in human leukemia U937 cells through the death receptor(exogenous)pathway,ROS-mediated regulation of the mitochondrial(endogenous)pathway,and the P38 MAPK signaling pathway.

参考文献/References:

[1]BAILEY,CLIFFORD J. Metformin:historical overview[J]. Diabetologia,2017,60:1566-1576.
[2]GOMES M B,RATHMANN W,CHARBONNEL B,et al. Treatment of type 2 diabetes mellitus worldwide:Baseline patient characteristics in the global DISCOVER study[J]. Diabetes research and clinical practice,2019,151:20-32.
[3]郑海珍,陈彩飞. 达英-35、二甲双胍联合克罗米芬治疗多囊卵巢综合征不孕患者的临床疗效[J]. 中国妇幼保健,2010,25(30):4431-4433.
[4]SHUBHA S,AMBLER G R,BAUR L A,et al. Randomized,controlled trial of metformin for obesity and insulin resistance in children and adolescents:improvement in body composition and fasting insulin[J]. Journal of clinical endocrinology and metabolism,2016,91(6):2074-2080.
[5]LI X,ZHANG X,KHAN I U,et al. The anti-tumor effects of the combination of microwave hyperthermia and lobaplatin against breast cancer cells in vitro and in vivo[J].Bioscience reports,2022,42(2):BSR20190878.
[6]LI P,ZHAO Q L,REHMAN M U,et al. Isofraxidin enhances hyperthermia-induced apoptosis via redox modification in acute monocytic leukemia U937 cells[J]. Molecular medicine reports,2023,27(2):46-87.
[7]PIAO J L,JIN Y J,LI M L,et al. Excessive oxidative stress in the synergistic effects of shikonin on the hyperthermia-induced apoptosis[J]. Current molecular medicine,2018,18(5):322-334.
[8]DAI G,LI Y,ZHANG M,et al. The regulation of the ampk/mtor axis mitigates tendon stem/progenitor cell senescence and delays tendon aging[J]. Stem cell reviews and reports,2023,16(9):126-137.
[9]尹春金. 人参皂苷 Re 对乙醇诱导的大鼠 H4IIE 肝细胞线粒体功能损伤的作用机制[D]. 吉林:延边大学,2022.
[10]JIKUN D,DAIBO S,JINWEN L,et al. Paeonol triggers apoptosis in HeLa cervical cancer cells:the role of mitochondria-related caspase pathway[J]. Psychopharmacology,2022,239(7):2083-2092.
[11]YANG Y,DAI Y,YANG X,et al. DNMT3A mutation-induced CDK1 overexpression promotes leukemogenesis by modulating the interaction between EZH2 and DNMT3A[J]. Biomolecules,2021,11(6):781.
[12]FAN X,ZHAO Z,MA L,et al. PTBP1 promotes IRES-mediated translation of cyclinB1 in cancer[J]. Acta biochimica et biophysica sinica,2022,54(5):696-707.
[13]WANG Y,HAN Y,WANG Y,et al. Expression of p38MAPK and its regulation of apoptosis under high temperature stress in the razor clam Sinonovacula constricta[J]. Fish & shellfish immunology,2022,122:288-297.
[14]马金苗,顼志兵,朱杰,等. 附萸汤改善心力衰竭大鼠的心室重构:基于抑制 AMPK/mTOR 通路介导的细胞自噬[J]. 南方医科大学学报,2023,43(3):466-473.
[15]CHEN N,LI P,LIU L,et al. Cucurbitacin IIb extracted from hemsleya penxianensis induces cell cycle arrest and apoptosis in bladder cancer cells by regulating cell cycle checkpoints and mitochondrial apoptotic pathway[J]. Plant foods for human nutrition,2023,23(1):56-80.
[16]SAHOO B M,BANIK B K,BORAH P,et al. Reactive Oxygen Species(ROS):Key components in cancer therapies[J]. Anticancer agents in medicinal chemistry,2022,22(2):215-222.
[17]NAKAMURA H,TAKADA K. Reactive oxygen species in cancer:Current findings and future directions[J]. Cancer science,2021,112(10):3945-3952.
[18]SAKAMURU S,ZHAO J,ATTENE-RAMOS M S,et al. Mitochondrial membrane potential assay[J]. Methods in molecular biology,2022,247(4):11-19.
[19]GREEN D R,KROEMER G. The pathophysiology of mitochondrial cell death[J]. Science,2004,305(5684):626-629.

相似文献/References:

[1]吴丹丹,裴丽丽,李冰艳,等.二甲双胍通过调控STAT3的表达抑制头颈部肿瘤转移机制的研究[J].南京师大学报(自然科学版),2019,42(01):107.[doi:10.3969/j.issn.1001-4616.2019.01.017]
 Wu Dandan,Pei Lili,Li Bingyan,et al.Metformin Inhibits the Metastasis of Head and Neck Cancerby Regulating the Expression of STAT3[J].Journal of Nanjing Normal University(Natural Science Edition),2019,42(03):107.[doi:10.3969/j.issn.1001-4616.2019.01.017]

备注/Memo

备注/Memo:
收稿日期:2023-07-13.
基金项目:中国科学院分离分析化学重点实验室开放基金项目(KL2208)、辽宁省教育厅面上项目(LJKMZ20221837).
通讯作者:史丽颖,副教授,研究方向:天然活性物质研究. E-mail:shiliying@dlu.edu.cn
更新日期/Last Update: 2024-09-15