|Table of Contents|

Salidroside suppresses proliferation and migration of non-small cell lung cancer cells via miRNA-210-3p/E2F3

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2023 04
Page:
625-631
Research Field:
Publishing date:

Info

Title:
Salidroside suppresses proliferation and migration of non-small cell lung cancer cells via miRNA-210-3p/E2F3
Author(s):
YANG Qi12 MING Yujun12 WANG Xiujuan12 JIANG Li2 CHEN Shaoping2
1.North Sichuan Medical College,Sichuan Nanchong 637000,China;2.Affiliated Hospital of North Sichuan Medical College,Sichuan Nanchong 637000,China.
Keywords:
salidrosidelung cancermiRNA-210-3pE2F3proliferationmigration
PACS:
R734.2
DOI:
10.3969/j.issn.1672-4992.2023.04.006
Abstract:
Objective:To investigate the effect and mechanism of salidroside (Sal) on proliferation and migration of non-small cell lung cancer (NSCLC) cells through miRNA-210-3p/E2F3.Methods:The expression and survival effects of miR-210-3p and target gene in lung adenocarcinoma tissues and normal tissues were analyzed by bioinformatics sites.Immunohistochemistry was used to detect the expression of E2F3 protein in lung adenocarcinoma tissues and normal tissues.qRT-PCR was used to detect the expression of miR-210-3p and E2F3 in NSCLC cells.Western blot was used to detect the expression of E2F3 protein in NSCLC cells.The effects of Sal and miR-210-3p on proliferation,migration and colony formation of NSCLC cells were determined by CCK-8 assay,scratch assay and colony formation assay,respectively.Results:Bioinformatics site showed that miR-210-3p and E2F3 were highly expressed in lung adenocarcinoma tissues and were associated with poor prognosis.Sal inhibited the proliferation activity of NSCLC cells in a time-concentration dependent manner (P<0.05),and significantly decreased the migration and colony formation ability of NSCLC cells (P<0.05),while low concentrations of Sal had no significant inhibitory effect on the proliferation of normal lung epithelial cells.miRNA-210-3p expression and E2F3 expression were upregulated in NSCLC cells (P<0.05),but Sal could inhibit their expression (P<0.05).Compared with the control group,the expression of E2F3 was increased in the miR-210-3p inhibitor group (P<0.05),inhibited in the miR-210-3p mimics group (P<0.05).The combination of Sal and miR-210-3p mimics further inhibited the downregulation of E2F3 expression induced by miR-210-3p mimics and the enhancement of NSCLC cell proliferation and migration (P<0.05).Conclusion:miR-210-3p and E2F3 were highly expressed in lung adenocarcinoma,and Sal could affect the biological behavior of NSCLC cells and exert anticancer effects via negative regulation of miRNA-210-3p/E2F3 in a time-concentration dependent manner.

References:

[1] ZHENG RS,ZHANG SW,ZENG HM,et al.Cancer incidence and mortality in China,2016[J].Journal of the National Cancer Center,2022,2(1):1-9.
[2] GAO SG,LI N,WANG SH,et al.Lung cancer in People's Republic of China[J].J Thorac Oncol,2020,15(10):1567-1576.
[3] SUN AQ,JU XL.Advances in research on anticancer properties of salidroside[J].Chin J Integr Med,2021,27(2):153-160.
[4] ZHAO Z,SUN W,GUO ZY,et al.Mechanisms of lncRNA/microRNA interactions in angiogenesis[J].Life Sci,2020,254:116900.
[5] PAN WM,WANG H,ZHANG XF,et al.miR-210 participates in hepatic ischemia reperfusion injuryby forming a negative feedback loop with SMAD4[J].Hepatolog,2020,72(6):2134-2148.
[6] SHAN H,LI XH,OUYANG C,et al.Salidroside prevents PM2.5-induced BEAS-2B cell apoptosis via SIRT1-dependent regulation of ROS and mitochondrial function[J].Ecotoxicol Environ Saf,2022,231:113170.
[7] ZHANG XM,XIE L,LONG JY,et al.Salidroside:A review of its recent advances in synthetic pathways and pharmacological properties[J].Chem Biol Interact,2021,339:109268.
[8] SUN SY,TUO QH,LI DX,et al.Antioxidant effects of salidroside in the cardiovascular system[J].Evid Based Complement Alternat Med,2020,2020:9568647.
[9] ALI SYEDA Z,LANGDEN SSS,MUNKHZUL C,et al.Regulatory mechanism of microRNA expression in cancer[J].Int J Mol Sci,2020,21(5):1723-1741.
[10] BAVELLONIi A,RAMAZZOTTI G,POLI A,et al.MiRNA-210:A current overview[J].Anticancer Research,2017,37(12):6511-6521.
[11] ZHANG HX,WU J,WU JH,et al.Exosome-mediated targeted delivery of miR-210 for angiogenic therapy after cerebral ischemia in mice[J].Journal of Nanobiotechnology,2019,17(1):29-52.
[12] GROSSO S,DOYEN J,PARKS SK,et al.MiR-210 promotes a hypoxic phenotype and increases radioresistance in human lung cancer cell lines[J].Cell Death & Disease,2013,4:e544.
[13] LIU D,XIA H,WANG F,et al.MicroRNA-210 interacts with FBXO31 to regulate cancer proliferation cell cycle and migration in human breast cancer[J].OncoTargets and Therapy,2016,9:5245-5255.
[14] XIE D,PEI Q,LI JY,et al.Emerging role of E2F family in cancer stem cells[J].Front Oncol,2021,11:723137.
[15] FENG ZC,PENG C,LI DJ,et al.E2F3 promotes cancer growth and is overexpressed through copy number variation in human melanoma[J].OncoTargets and Therapy,2018:11:5303-5313.
[16] SUN FB,LIN Y,LI SJ,et al.MiR-210 knockdown promotes the development of pancreatic cancer via upregulating E2F3 expression[J].European Review for Medical and Pharmacological Sciences,2018,22(24):8640-8648.
[17] JIN Y,WEI J,XU ST,et al.miR-210-3pregulates cell growth and affects cisplatin sensitivity in human ovarian cancer cells via targeting E2F3[J].Molecular Medicine Reports,2019,19(6):4946-4954.
[18] HUANG LT,HUANG ZX,LIN WJ,et al.Salidroside suppresses the growth and invasion of human osteosarcoma cell lines MG63 and U2OS in vitro by inhibiting the JAK2/STAT3 signaling pathway[J].Int J Oncol,2019,54(6):1969-1980.
[19] DING SY,WAGN MT,DAI DF,et al.Salidroside induces apoptosis and triggers endoplasmic reticulum stress in human hepatocellular carcinoma[J].Biochem Biophys Res Commun,2020,527(4):1057-1063.
[20] ZHANG X,ZHU JL,YAN JN,et al.Systems pharmacology unravels the synergic target space and therapeutic potential of Rhodiola rosea L.for non-small cell lung cancer[J].Phytomedicine,2020,79:153326.
[21] ZHANG ZD,YANG W,MA F,et al.Enhancing the chemotherapy effect of Apatinib on gastric cancer by co-treating with salidroside to reprogram the tumor hypoxia micro-environment and induce cell apoptosis[J].Drug Deliv,2020,27(1):691-702.

Memo

Memo:
四川省医学会(恒瑞)科研基金专项科研课题(编号:2021HR24);四川省科技计划项目(编号:2020YFS0572);四川省南充市2022年市校科技战略合作专项(编号:22SXQT0152)
Last Update: 1900-01-01