Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8309387 | Clinica Chimica Acta | 2018 | 5 Pages |
Abstract
Long non-coding RNAs (lncRNAs), a novel class of noncoding RNAs, are commonly defined as RNA molecules more than 200 nucleotides in length. Emerging research indicated that lncRNA played a vital role in human tumorigenesis and progression by serving as tumor oncogenes or suppressors. LncRNA has been shown to get involved in participate various biological processes, such as cell growth, anti-apoptosis, migration and invasion. LncRNA HOXA cluster antisense RNA2 (HOXA-AS2) is a novel cancer-related lncRNA. It was recently found to exhibit aberrant expression in a variety of malignancies, including breast cancer, gastric cancer, gallbladder carcinoma, hepatocellular carcinoma and pancreatic cancer. The oncogenicity of lncRNA HOXA-AS2 mainly inhibits or promotes the expression of related genes through direct or indirect pathways, suggesting that HOXA-AS2 likely represents a feasible biomarker or therapeutic target in human cancers. In this review, we summarize current evidences concerning the biological functions and mechanisms of HOXA-AS2 during tumor development.
Keywords
TGFBR2EZH2LSD1KLF2ncRNAslncRNAsPRC2Bcl-2NF-kBDdit3APLBCL2-Associated XMatrix metalloproteinase-2/9MYC Proto-OncogeneKruppel like factor 2transforming growth factor beta receptor 2EGFRTGF-βmiRNAsPlk3MMP-2/9GBClncRNAatRAc-MycHCCLong non-coding RNAsVE-cadherinVascular endothelial-cadherinBaxTransforming growth factor βTerminal deoxynucleotidyl transferase-mediated dUTP nick end labelingDiagnosisall trans retinoic acidTUNELEMTlysine specific demethylase 1RelAmicroRNAsColorectal cancerGastric cancerPancreatic cancerBreast cancerTRAILB-cell lymphoma-2Acute promyelocytic leukemiaTNF-related apoptosis-inducing ligandTherapeutic targetprognosispolycomb repressive complex 2Hepatocellular carcinomaGallbladder carcinomaCRCEpithelial-mesenchymal transitionEpidermal growth factor receptor
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Authors
Jicai Wang, Zhilei Su, Shounan Lu, Wen Fu, Zhifa Liu, Xingming Jiang, Sheng Tai,