|Table of Contents|

Expression and clinical significance of LINC01006 in esophageal cancer tissue

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

Issue:
2025 05
Page:
764-771
Research Field:
Publishing date:

Info

Title:
Expression and clinical significance of LINC01006 in esophageal cancer tissue
Author(s):
FANG Zhenghua1ZHU Chen1DU Mingyu2XIE Peng1
1.Anqing Second People's Hospital,Anhui Anqing 246000,China;2.Jiangsu Cancer Hospital,Jiangsu Nanjing 210000,China.
Keywords:
LINC01006esophageal squamous cell carcinomainvasionmiR-449c
PACS:
R735.1
DOI:
10.3969/j.issn.1672-4992.2025.05.007
Abstract:
Objective:To investigate the expression,clinical significance of lncRNA LINC01006 in esophageal squamous cell carcinoma (ESCC),and to explore its possible mechanism of action.Methods:The tumors and corresponding adjacent tissues were collected from 60 patients with ESCC treated in our hospital from January 2016 to July 2019.RT-qPCR was used to detect LINC01006 expression in tissue.The relationship between LINC01006 expression and clinical features,overall survival (OS) of patients was analyzed.The effect of silencing LINC01006 on the proliferation,invasion of esophageal cancer cells was explored by CCK8 and Transwell experiments.Dual-luciferase reporter assay was employed to identify the relationship between miR-449c and LINC01006.Results:The results of RT-qPCR assay showed that LINC01006 expression in ESCC tissue was significantly higher than the corresponding adjacent tissues(5.755±2.602 vs 1.406±0.077,P<0.01).And its expression level was closely related to the TNM stage of patients by Chi-quare test (P<0.01).The results of Kaplan-Meier analysis indicated that the OS of patients with high expression of LINC01006 was significantly shorter than those with low expression(P<0.01).Cox regression univariate and multivariate analysis showed that the expression of LINC01006 was an independent risk factor for OS (HR=4.245,95%CI:1.589~11.338,P=0.004;HR=3.356,95%CI:1.185~9.509,P=0.023) in patients with ESCC.Cell biological experiments exhibited that LINC01006 knockdown significantly reduced the proliferation,invasion of ESCC cells.Dual-luciferase reporter assay showed that miR-449c directly targeted LINC01006.The results of rescue experiments indicated that inhibition of miR-449c expression reversed the inhibition of tumor cell activity caused by silencing LINC01006.Western blot experimental result further validated that LINC01006 can activate the expression of MET protein by competitive binding to miR-449c.Conclusion:LINC01006 is significantly overexpressed in ESCC tissue and cells.Knocking down LINC01006 can inhibit the proliferation and invasion abilities of tumor cells via miR-449c-MET axis,which is able to be a new treatment target of ESCC.

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Memo

Memo:
National Natural Science Foundation of China(No.82002870);国家自然科学基金(编号:82002870)
Last Update: 1900-01-01