|Table of Contents|

miR-573 promotes epithelial-mesenchymal transition of lung cancer cells by regulating Netrin-4

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

Issue:
2023 12
Page:
2228-2234
Research Field:
Publishing date:

Info

Title:
miR-573 promotes epithelial-mesenchymal transition of lung cancer cells by regulating Netrin-4
Author(s):
XIAO LeiXU DanyuanDUAN LinliHE Mengzhang
Department of Respiratory Medicine,Panyu District,the Second Affiliated Hospital of Guangzhou Medical University,Guangdong Guangzhou 510140,China.
Keywords:
miR-573Netrin-4lung cancerepithelial-mesenchymal transition
PACS:
R734.2
DOI:
10.3969/j.issn.1672-4992.2023.12.010
Abstract:
Objective:To investigate the effect of miR-573 on the epithelial-mesenchymal transition(EMT) of lung cancer cells by regulating Netrin-4 (NTN4).Methods:Real-time fluorescent quantitative PCR(qRT-PCR) was used to detect the levels of miR-573 and NTN4 mRNA in human lung cancer tissues and cell lines.Lung cancer A549 cells were transfected with Lipofectamine 2000 transfection reagent and grouped into control group(not transfected),NC inhibitor group(transfected with NC inhibitor),miR-573 inhibitor group (transfected with miR-573 inhibitor),miR-573 inhibitor+si-NC group(transfected with miR-573 inhibitor and si-NC) and miR-573 inhibitor+si-NTN4 group(transfected with miR-573 inhibitor and si-NTN4).qRT-PCR was used to detect the expression level of miR-573.Scratch method was used to detect the migration ability.Transwell cell method was used to detect the invasion and migration abilities.Western blot was used to detect the expression levels of NTN4,E-cadherin,N-cadherin and Vimentin.Dual luciferase experiment was used to verify the targeting relationship between miR-573 and NTN4.Results:The expression of miR-573 was significantly increased and the expression of NTN4 mRNA was significantly decreased in lung cancer tissues and cell lines (P<0.05).The A549 cells with the highest relative expression of miR-573 were selected for transfection experiments.Compared with the control group or NC inhibitor group,the relative expression of miR-573 and the protein levels of N-cadherin and Vimentin in the A549 cells of the miR-573 inhibitor group were significantly decreased.The scratch healing rate was significantly reduced.The numbers of migrating and invading cells were significantly reduced,and the level of E-cadherin protein was significantly increased (P<0.05).miR-573 negatively regulated NTN4 expression (P<0.05).Transfection of si-NTN4 could reverse the inhibitory effects of miR-573 inhibitor on migration,invasion and EMT of A549 cells (P<0.05).Conclusion:miR-573 targets and negatively regulates the expression of NTN4 and promotes the migration,invasion and EMT of lung cancer cells.

References:

[1] FENG RM,ZONG YN,CAO SM,et al.Current cancer situation in China:good or bad news from the 2018 global cancer statistics[J].Cancer Commun (Lond),2019,39(1):22-34.
[2] SAYAN M,SATIR TURK M,CELIK A,et al.Surgical outcomes of early-stage small-cell lung cancer:single-center experience[J].Asian Cardiovasc Thorac Ann,2019,27(3):187-191.
[3] LIANG G,MENG W,HUANG X,et al.miR-196b-5p-mediated downregulation of TSPAN12 and GATA6 promotes tumor progression in non-small cell lung cancer[J].Proc Natl Acad Sci USA,2020,117(8):4347-4357.
[4] GAO L,YAN SB,YANG J,et al.miR-182-5p and its target HOXA9 in non-small cell lung cancer:a clinical and in-silico exploration with the combination of RT-qPCR,miRNA-seq and miRNA-chip[J].BMC Med Genomics,2020,13(1):3-23.
[5] SHEN L,YI S,HUANG L,et al.miR-330-3p promotes lung cancer cells invasion,migration,and metastasis by directly targeting hSOD2b[J].Biotechnol Appl Biochem,2019,66(1):21-32.
[6] LIAO M,PENG L.miR-206 may suppress non-small lung cancer metastasis by targeting CORO1C[J].Cell Mol Biol Lett,2020,25(1):22-35.
[7] LIANG Z,XU J,MA Z,et al.miR-187 suppresses non-small-cell lung cancer cell proliferation by targeting FGF9[J].Bioengineered,2020,11(1):70-80.
[8] JIANG X,LI M,KE L.miR-34c regulates the proliferation and apoptosis of lung cancer cells[J].Clin Invest Med,2020,43(4):E56-62.
[9] PENGCHENG Z,PENG G,HAOWEN F,et al.miR-573 suppresses cell proliferation,migration and invasion via regulation of E2F3 in pancreatic cancer[J].J Cancer,2021,12(10):3033-3044.
[10] 陈志平,王岚枫,衷敬华,等.miR-573调控载脂蛋白M促进肝细胞迁移的机制研究[J].中国临床药理学杂志,2020,36(20):3260-3263. CHEN ZP,WANG LF,ZHONG JH,et al.miR-573 regulates the mechanism of apolipoprotein M promoting hepatocyte migration[J].Chin J Clinical Pharmacology,2020,36(20):3260-3263.
[11] XU X,YAN Q,WANG Y,et al.NTN4 is associated with breast cancer metastasis via regulation of EMT-related biomarkers[J].Oncol Rep,2017,37(1):449-457.
[12] XU K,SHI J,MO D,et al.miR-219a-1 inhibits colon cancer cells proliferation and invasion by targeting MEMO1[J].Cancer Biol Ther,2020,21(12):1163-1170.
[13] MAIMAITIMING A,WUSIMAN A,AIMUDULA A,et al.MicroRNA-152 inhibits cell proliferation,migration,and invasion in breast cancer[J].Oncol Res,2020,28(1):13-19.
[14] WU T,SONG H,XIE D,et al.miR-30b-5p promotes proliferation,migration,and invasion of breast cancer cells via targeting ASPP2[J].Biomed Res Int,2020,2020(1):7907269-7907281.
[15] WANG L,GAO P,YUAN P,et al.miR-573 suppresses pancreatic cancer cell proliferation,migration,and invasion through targeting TSPAN1[J].Strahlenther Onkol,2021,197(5):438-448.
[16] AIELLO NM,KANG Y.Context-dependent EMT programs in cancer metastasis[J].J Exp Med,2019,216(5):1016-1026.
[17] WANG H,HU X,YANG F,et al.miR-325-3p promotes the proliferation,invasion,and EMT of breast cancer cells by directly targeting S100A2[J].Oncol Res,2021,28(7):731-744.
[18] YI L,LEI Y,YUAN F,et al.NTN4 as a prognostic marker and a hallmark for immune infiltration in breast cancer[J].Sci Rep,2022,12(1):10567.
[19] LI L,HUANG Y,GAO Y,et al.EGF/EGFR upregulates and cooperates with Netrin-4 to protect glioblastoma cells from DNA damage-induced senescence[J].BMC Cancer,2018,18(1):1215-1225.
[20] WANG Y,XU W,WANG Y,et al.miR-17-5p promotes migration and invasion in breast cancer cells by repressing netrin 4[J].Int J Clin Exp Pathol,2019,12(5):1649-1657.
[21] LI C,HOU X,YUAN S,et al.High expression of TREM2 promotes EMT via the PI3K/AKT pathway in gastric cancer:bioinformatics analysis and experimental verification[J].J Cancer,2021,12(11):3277-3290.

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