LINC00467: A key oncogenic long non-coding RNA
Language English Country Netherlands Media print-electronic
Document type Journal Article, Review
PubMed
36122666
DOI
10.1016/j.cca.2022.09.013
PII: S0009-8981(22)01302-X
Knihovny.cz E-resources
- Keywords
- Cancer, LINC00467, Oncogene, lncRNA, miRNA,
- MeSH
- beta Catenin genetics MeSH
- Biomarkers MeSH
- Carcinogenesis genetics MeSH
- Humans MeSH
- MicroRNAs * genetics MeSH
- Cell Line, Tumor MeSH
- Neoplasms * genetics MeSH
- NF-kappa B MeSH
- Oncogenes genetics MeSH
- Cell Proliferation genetics MeSH
- Proto-Oncogene Proteins c-akt genetics MeSH
- Gene Expression Regulation, Neoplastic MeSH
- RNA, Long Noncoding * genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- beta Catenin MeSH
- Biomarkers MeSH
- MicroRNAs * MeSH
- NF-kappa B MeSH
- Proto-Oncogene Proteins c-akt MeSH
- RNA, Long Noncoding * MeSH
The significance of long non-coding RNAs (lncRNAs) in the development and progression of human cancers has attracted increasing attention in recent years of investigations. Having versatile interactions and diverse functions, lncRNAs can act as oncogenes or tumor-suppressors to actively regulate cell proliferation, survival, stemness, drug resistance, invasion and metastasis. LINC00467, an oncogenic member of long intergenic non-coding RNAs, is upregulated in numerous malignancies and its high expression is often related to poor clinicopathological features. LINC00467 facilitates the progression of cancer via sponging tumor-suppressive microRNAs, inhibiting cell death cascade, modulating cell cycle controllers, and regulating signalling pathways including AKT, STAT3, NF-κB and Wnt/β-catenin. A growing number of studies have revealed that LINC00467 may serve as a novel prognostic biomarker and its inhibitory targeting has a valuable therapeutic potential to suppress the malignant phenotypes of cancer cells. In the present review, we discuss the importance of LINC00467 and provide a comprehensive collection of its functions and molecular mechanisms in a variety of cancer types.
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