LINC00941: a novel player involved in the progression of human cancers.
Qibin YanXinming SuYunzhu ChenZehua WangWenbo HanQing XiaYunan MaoJiahua SiHanbing LiShiwei DuanPublished in: Human cell (2023)
LINC00941, also known as lncRNA-MUF, is an intergenic non-coding RNA located on chromosome 12p11.21. It actively participates in a complex competing endogenous RNA network, regulating the expression of microRNA and its downstream proteins. Through transcriptional and post-transcriptional regulation, LINC00941 plays a vital role in multiple signaling pathways, influencing cell behaviors such as tumor cell proliferation, epithelial-mesenchymal transition, migration, and invasion. Noteworthy is its consistently high expression in various tumor types, closely correlating with clinicopathological features and cancer prognoses. Elevated LINC00941 levels are associated with adverse clinical outcomes, including increased tumor size, extensive lymphatic metastasis, and distant metastasis, leading to poorer survival rates across different cancers. Additionally, LINC00941 and its associated genes are linked to various targeted drugs available in the market. In this comprehensive review, we systematically summarize existing studies, detailing LINC00941's differential expression, clinicopathological and prognostic implications, regulatory mechanisms, and associated therapeutic drugs. Our analysis includes relevant charts and incorporates bioinformatics analyses to verify LINC00941's differential expression in pan-cancer and explore potential transcriptional regulation patterns of downstream targets. This work not only establishes a robust data foundation but also guides future research directions. Given its potential as a significant cancer biomarker and therapeutic target, further investigation into LINC00941's differential expression and regulatory mechanisms is essential.
Keyphrases
- long non coding rna
- cell proliferation
- long noncoding rna
- poor prognosis
- papillary thyroid
- epithelial mesenchymal transition
- squamous cell
- transcription factor
- cell cycle
- pi k akt
- lymph node
- gene expression
- stem cells
- childhood cancer
- squamous cell carcinoma
- emergency department
- oxidative stress
- single cell
- cell therapy
- dna methylation
- copy number
- pluripotent stem cells
- endoplasmic reticulum stress