小RNA
生物标志物
癌症
CD44细胞
疾病
转移
染色质
癌症研究
癌症干细胞
生物
生物信息学
医学
计算生物学
细胞
癌细胞
核糖核酸
基因表达调控
细胞周期
转录组
染色质重塑
基因表达
生物标志物发现
诊断生物标志物
靶向治疗
电池类型
基因
循环肿瘤细胞
干细胞
竞争性内源性RNA
调节器
遗传增强
肿瘤发生
精密医学
治疗方法
信号转导
肿瘤科
作者
Haoran Liu,Yining Pan,Haoyi Liu,Yuxiang Peng,Xu Zheng,Yan Zhang,Zhouya Xu,Zhaoying Tang,Enduo Yan,Yutong Wu,Haodong He,Gang Zhou,Chengfu Yuan
标识
DOI:10.2174/0113816128455595260309062416
摘要
Long non-coding RNAs (lncRNAs) have garnered significant attention recently since they are fundamental to many biological processes, including gene expression, chromatin remodeling, and cell cycle control. Among these, the gastric adenocarcinoma-associated positive CD44 regulator, long intergenic non-coding RNA (GAPLINC), plays a crucial role in tumor biology. GAPLINC interacts with microRNAs (miRNAs) and RNA-binding proteins to control important oncogenic pathways, including cancer cell proliferation, migration, invasion, and Epithelial-Mesenchymal Transition (EMT), as a competitive endogenous RNA (ceRNA). GAPLINC's potential as both a prognostic biomarker and a therapeutic target is highlighted by its dysregulated expression in cancer tissues, which is associated with poor prognosis and enhanced disease aggressiveness. This review focuses on the interactions of GAPLINC with miRNAs, RNA-binding proteins, and key signaling pathways, and it investigates the molecular routes through which it shapes tumor cell biology. Moreover, GAPLINC's participation in EMT and cancer stem cell control emphasizes its importance in carcinogenesis, disease development, and therapy resistance. GAPLINC has great promise for individualized cancer treatment, given its several functions in the disease. Future studies should seek to confirm GAPLINC's clinical relevance, look at its therapeutic potential, and create focused RNA-based inhibitory techniques. Such initiatives might open the path for better patient outcomes for a variety of cancer types and more efficient therapies.
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