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Category | LncRNA | Biological function/phenotypes | Molecular mechanisms/targets | Survival correlation | Others | References |
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Overrepresented in gliomas | HOTAIR | Maintains proliferation and tumorigenic potential of GBM cells | Associating with PRC2; regulating Wnt/β-catenin signaling; ceRNAs (competing endogenous RNAs) for miR-326 and miR-148b-3p | Yes | Preferentially expressed in classical and mesenchymal glioma | [64–67] |
CRNDE | Promotes glioma cell growth and migration in vitro and tumorigenesis in a xenograft mouse mode | ceRNAs for miR-136-5p, miR-186, and miR-384 | Yes | | [55, 71–73] |
NEAT1 | Promotes glioma pathogenesis | ceRNAs for miR-449b-5p to upregulate c-Met; associating with EZH2 | Yes | | [78–80] |
XIST | Confers glioma cells’ oncogenic and chemoresistant behaviors; XIST knockdown increased permeability of the brain-tumor barrier (BTB) and inhibited glioma angiogenesis | ceRNAs for miR-152, miR-429, miR-29c, and miR-137 | / | | [14, 83–86] |
H19 | Enhances invasion, angiogenesis, stemness and tumorigenicity of GBM cells; depletion of H19 inhibited glioma-provoked proliferation, migration, and tube formation of glioma endothelial cells (GECs) | ceRNA (miR-29a); negatively regulating RB1 expression | Yes | | [12, 89, 92, 93] |
TUG1 | Maintains stemness and tumorigenic properties of GBM stem-like cells (GSCs); modulates blood-tumor barrier; and enhances glioma-induced angiogenesis | Associating with PRC2 and YY1; ceRNAs for miR-26a, miR-144, miR-299, and miR-145 | / | Intravenous administration of ASOs against TUG1 induces GSC differentiation and suppresses tumor growth intracranially | [46, 125–127] |
SOX2OT | Maintains proliferation, migration, invasion, and tumorigenesis of GSCs | ceRNAs for miR-122 and miR-194-5p | / | | [99] |
UCA1 | Promote glioma cell proliferation, invasion, and migration; modulates glioblastoma-associated stromal cell-mediated glycolysis and invasion of glioma cells | ceRNAs for miR-182 and miR-122 | Yes | | [165–168] |
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Downregulated in gliomas | MEG3 | Impairs in vitro glioma cell proliferation | MDM2-p53; ceRNAs for miR-19a and miR-93 | / | | [105–109] |
MALAT1 | Tumor-suppressive function in glioma | Inactivating the ERK/MAPK signaling; enhancing the expression of tumor-suppressor FBXW7 | Yes | MALAT1 could be either a positive or a negative regulator in glioma tumorigenesis depending on cellular contexts | [115–119] |
ROR | Tumor-suppressive function in glioma | ROR’s expression is negatively correlated with the level of KLF4, a stem cell gene | / | | [169] |
TUSC7 | Suppresses cellular proliferation and invasion of glioma cells, accelerates cellular apoptosis, and inhibits TMZ resistance | ceRNAs for miR-23b and miR-10a | Yes | | [170–172] |
CASC2 | CACS2 overexpression sensitizes glioma cells to TMZ | ceRNAs for miR-181a and miR-193-5p to upregulate PTEN and mTOR expression | Yes | | [134–136] |
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