|Table of Contents|

Influence of LINC01296 on cisplatin resistance in ovarian cancer by regulating Wnt/β-catenin pathway

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

Issue:
2023 20
Page:
3770-3776
Research Field:
Publishing date:

Info

Title:
Influence of LINC01296 on cisplatin resistance in ovarian cancer by regulating Wnt/β-catenin pathway
Author(s):
LIN FangtingWU QingyuWANG RuLI Bo
Department of Gynecology,Hainan Women and Children Medical Center,Hainan Haikou 570100,China.
Keywords:
long non-coding RNA LINC01296Wnt/β-catenin pathwayovarian cancercisplatin resistance
PACS:
R737.31
DOI:
10.3969/j.issn.1672-4992.2023.20.009
Abstract:
Objective:To investigate the influence of long non-coding RNA LINC01296 on cisplatin resistance in ovarian cancer by regulating Wnt/β-catenin pathway.Methods:Human ovarian cancer SKOV3 cells and SKOV3 cisplatin-resistant SKOV3/DDP cells were cultured,and the expression of LINC01296 was detected by qRT-PCR.SKOV3/DDP cells were separated into 5 groups:Control group (normal culture),si-NC group (transfected with si-NC),si-LINC01296 group (transfected with si-LINC01296),si-NC+LiCl group (transfected with si-NC+Wnt/β-catenin pathway agonist LiCl 10 mmol/L treatment),and si-LINC01296+LiCl group (transfected with si-LINC01296+10 mmol/L LiCl treatment).qRT-PCR was used to verify the transfection effect.The median inhibitory concentration (IC50) of cisplatin in SKOV3/DDP cells in each group (0,1,2,4,8,16,32 μg/mL cisplatin treatment) and proliferation activity were determined by CCK-8 method.The apoptosis of SKOV3/DDP cells in each group was detected by flow cytometry.The migration ability of SKOV3/DDP cells in each group was detected by scratch healing test.The expression of Wnt/β-catenin pathway and proliferation,apoptosis,migration and invasion-related proteins Ki67.B-cell lymphoma/leukemia gene-2-associated X protein gene (Bax),matrix metalloproteinase 9 (MMP9),N-cadherin in SKOV3/DDP cells in each group was detected by Western Blot.Results:The expression level of LINC01296 in SKOV3/DDP cells was obviously higher than that in SKOV3 cells (P<0.05).After SKOV3/DDP cells were transfected with si-LINC01296,the expression level of LINC01296 was obviously lower than that in the control group and si-NC group (P<0.05),indicating that the transfection was successful.Compared with the control group,the cisplatin IC50,proliferation activity,healing rate of cell scratch and invasion number of SKOV3/DDP cells all decreased in the si-LINC01296 group,the apoptosis rate increased,the protein expression of β-catenin,Ki67,MMP9,and N-cadherin decreased,and the protein expression of Bax increased (P<0.05).Compared with si-LINC01296 group,the cisplatin IC50,proliferation activity,healing rate of cell scratch and invasion number of SKOV3/DDP cells all increased in the si-LINC01296+LiCl group,the apoptosis rate decreased,the protein expression of β-catenin,Ki67,MMP9,and N-cadherin increased,and the protein expression of Bax decreased (P<0.05).Conclusion:Knockdown of LINC01296 can reduce cisplatin resistance in SKOV3/DDP cells,possibly by inhibiting the Wnt/β-catenin pathway.

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海南省卫生计生行业科研项目(编号:20A200035)
Last Update: 1900-01-01