The regulatory role and therapeutic potential of long non-coding RNA in non-small cell lung cancer

被引:0
|
作者
Xia, Sunming [1 ,2 ]
Lu, Xuean [1 ,2 ]
Wang, Weier [3 ]
Pan, Xinyi [4 ]
Cui, Jiaqi [4 ]
Wang, Shengjie [1 ,4 ]
Wang, Zhao [5 ]
机构
[1] Nanjing Med Univ, Donghai Cty Peoples Hosp, Kangda Coll, Lianyungang 222300, Jiangsu, Peoples R China
[2] Donghai Cty Peoples Hosp, Dept Gen Surg, Lianyungang 222300, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Med, Nanjing 210023, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Kangda Coll, Dept Basic Med, Lianyungang 222000, Jiangsu, Peoples R China
[5] Soochow Univ, Dept Oncol, Affiliated Hosp 1, Suzhou 215006, Jiangsu, Peoples R China
来源
JOURNAL OF CANCER | 2025年 / 16卷 / 04期
基金
中国国家自然科学基金;
关键词
LncRNAs; proliferation; metastasis; targeted therapies; NSCLC; UP-REGULATION; PROLIFERATION; LNCRNA; APOPTOSIS; MIGRATION; EXPRESSION; BIOMARKERS; MICRORNA; GAS5;
D O I
10.7150/jca.103182
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer remains the leading cause of cancer-related mortality worldwide, with non-small cell lung cancer (NSCLC) being the predominant subtype. Recent advances in transcriptome sequencing have highlighted the critical role of long non-coding RNAs (lncRNAs) in NSCLC, with lncRNAs influencing gene expression through epigenetic, transcriptional, and post-transcriptional mechanisms. Despite the growing understanding of lncRNAs, challenges such as delayed diagnosis and drug resistance continue to complicate NSCLC management. This review explores novel findings in the role of lncRNAs (e.g., MALAT1, HOTAIR, and GAS5) in NSCLC, with a particular focus on their encoded small peptides and N6-methyladenosine (m6A) modifications. We further discuss how the interplay between lncRNAs, their encoded peptides, and m6A modifications can provide new strategies for improving NSCLC diagnosis, treatment, and overcoming drug resistance. This review also highlights emerging research avenues that could lead to innovative clinical interventions in NSCLC.
引用
收藏
页码:1137 / 1148
页数:12
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