LncRNA Information
ID EL0333 Name DBH-AS1 Aliases NCRNA00118
Species Homo sapiens Chromosome 9 Start site 133654586
End site 133657313 Chain minus Exon NO. 2
Assembly Ensembl Release 89 Class antisense NCBI accession NR_102735
Ensembl ENSG00000225756 Sequence


Disease
Disease Method Sample Expression pattern Dysfunction type Description PMID Source
hepatocelluar carcinoma qPCR, Western blot, knockdown etc. HCC tissue, cell lines (HepG2, SMMC-7721, Hep3B, MHCC97H, SK-Hep1) up-regulated interaction The levels of DBH-AS1 were positively correlated with hepatitis B surface antigen (HBsAg) and tumor size in HCC tissues. Overexpression of DBH-AS1 induced cell cycle progression by accelerating G1/S and G2/M transition concomitantly with upregulation of CDK6, CCND1, CCNE1 and downregulation of p16, p21 and p27. We also provide evidence that DBH-AS1 could be significantly induced by HBx protein and markedly down-regulated by p53. Thus, we concluded that DBH-AS1 can be induced by HBx and inactivated by p53, and consequently promote cell proliferation and cell survival through activation of MAPK signaling in HCC. 26393879 Lnc2Cancer
 


Interaction
Interaction target Level of interaction Type of interaction Description PMID Source
hepatitis B virus x protein (HBx) RNA-Protein regulation DBH-AS1 could be significantly induced by HBx protein and markedly down-regulated by p53. 26393879
p53 RNA-Protein regulation DBH-AS1 could be significantly induced by HBx protein and markedly down-regulated by p53. 26393879
MAPK signaling N/A regulation DBH-AS1 was shown to activate MAPK pathway. 26393879
CDK6, CCND1, CCNE1 RNA-Protein regulation Overexpression of DBH-AS1 induced cell cycle progression by accelerating G1/S and G2/M transition concomitantly with upregulation of CDK6, CCND1, CCNE1 and downregulation of p16, p21 and p27. 26393879
p16, p21 and p27 RNA-Protein regulation Overexpression of DBH-AS1 induced cell cycle progression by accelerating G1/S and G2/M transition concomitantly with upregulation of CDK6, CCND1, CCNE1 and downregulation of p16, p21 and p27. 26393879