Roles of Wnt/β-Catenin Signaling Pathway Regulatory Long Non-Coding RNAs in the Pathogenesis of Non-Small Cell Lung Cancer

被引:29
作者
Lin, Shan [1 ,2 ,3 ]
Zhen, Yu [4 ]
Guan, Yinghui [3 ]
Yi, Huanfa [1 ,2 ]
机构
[1] Jilin Univ, Hosp 1, Cent Lab, Changchun, Jilin, Peoples R China
[2] Minist Educ, Key Lab Organ Regenerat & Transplantat, Changchun 130021, Jilin, Peoples R China
[3] Jilin Univ, Hosp 1, Dept Resp, Changchun, Jilin, Peoples R China
[4] Jilin Univ, Hosp 1, Dept Dermatol, Changchun, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
long non-coding RNA; lung cancer; non-small cell lung cancer; pathogenesis; Wnt/beta-catenin signaling; DOWN-REGULATION; UP-REGULATION; NEAT1; ACTS; PROLIFERATION; METASTASIS; PROMOTES; PROGRESSION; ACTIVATION; APOPTOSIS; GROWTH;
D O I
10.2147/CMAR.S241519
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is one of the leading causes of cancer-related mortality worldwide. Non-small cell lung cancer (NSCLC) is the most common pathological type of lung cancer. Long non-coding RNAs (lncRNAs) are promising novel diagnostic and prognostic biomarkers, as well as potential therapeutic targets for lung cancer. Long non-coding RNAs (lncRNAs) have been demonstrated to modulate tumor cells proliferation, cell cycle progression, invasion, and metastasis by regulating gene expression at transcriptional, post-transcriptional, and epigenetic levels. The oncogenic aberrant Wnt/beta-catenin signaling is prominent in lung cancer, playing a vital role in tumorigenesis, prognosis, and resistance to therapy. Interestingly, compelling studies have demonstrated that lncRNAs exert either oncogenic or tumor suppressor roles by regulating Wnt/beta-catenin signaling. In this review, we aim to present the current accumulated knowledge regarding the roles of Wnt/beta-catenin signaling-regulated lncRNAs in the pathogenesis of non-small cell lung cancer (NSCLC). Better understanding of the effects of lncRNAs on Wnt/beta-catenin signaling might contribute to the improved understanding of the molecular tumor pathogenesis and to the uncovering of novel therapeutic targets in NSCLC.
引用
收藏
页码:4181 / 4191
页数:11
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