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. 2012 Oct 2;47(1):131–144. doi: 10.1007/s12035-012-8349-7

Table 3.

miRNAs with disputed expression levels and their functional role in GBM

miRNA Target Functional role when overexpressed Functional role when underexpressed References
Overexpression in GBM Underexpression in GBM
Hsa-mir-19a CTGF Viability↓, Apoptosis↑, Proliferation↓ [2426, 30] [34]
Hsa-mir-26b EphA2a Proliferation↓, Invasiveness↓, Angiogenesis↓ [31] [26, 107]
Hsa-mir-27b WEE1 Proliferation↓, Apoptosis↑, Invasiveness↓ [126] [25]
Hsa-mir-106a E2F1 Proliferation↓, Apoptosis↑ [24, 26, 35] [45, 127]
Hsa-mir-143 Invasiveness↓ [6] [26]
Hsa-mir-145bc Oct4, SOX2 In vivo tumor volume↓, Migration↓, Stemness↓, Chemosensitivity↑, Radiosensitivity↑ Invasiveness↓ [6, 86] [11]
Hsa-mir-205 VEGF-Aa Proliferation↓, Apoptosis↑, Invasiveness↓ [26] [99]
Hsa-mir-451b PI3K/Akt-pathway, CAB39a Proliferation↓, Invasion↓, Stemness↓, Neurosphere formation↓, Proliferation↑ Migration↑ [23, 87, 89] [35, 52, 88, 89]

miRNAs found to be both up- and downregulated in GBM and their functional role. The table presents miRNAs, which have been reported with differential expression levels in GBM between different research groups. Only miRNAs that are investigated in greater than or equal to five studies and/or have a validated target are included in this table. The effects of upregulation or downregulation and validated targets are presented. The cell lines applied in the annotated studies can be found in Supplementary Table 1

aTargets involved in the mesenchymal mode of migration and invasion

bMentioned in the section “miRNAs with disputed expression levels”

cmiRNAs whose upregulation is shown to inhibit tumor growth in vivo