Basic Information
LncRNA/CircRNA Name | LINC00152 |
Synonyms | CYTOR, C2orf59, LINC00152, NCRNA00152 |
Region | GRCh38_2:87454781-87636740 |
Ensemble | ENSG00000222041 |
Refseq | NR_024204 |
Classification Information
Regulatory Mechanism | Biological Function | Clinical Application | |||
---|---|---|---|---|---|
TF | Immune | Survival | |||
Enhancer | Apoptosis | Drug | |||
Variant | Cell Growth | Circulating | |||
MiRNA | EMT | Metastasis | |||
Methylation | Coding Ability | Recurrence |
Cancer&Entry Information
Cancer Name | gallbladder cancer |
ICD-0-3 | C23.9 |
Methods | qPCR, RNAi, Western blot, ChIP, Luciferase reporter assay, Cell proliferation assay etc. |
Sample | GBC tissues, cell lines (EH-GB2, GBC-SD, NOZ, SGC-996) |
Expression Pattern | up-regulated |
Function Description | In this study, we report that the long non-coding RNA LINC00152 is significantly upregulated in GBC tissues and cell lines. The high LINC00152 levels correlated positively with tumor status progression, lymph node invasion and TNM stage advancement. Functionally, we revealed that LINC00152 dramatically promoted cell proliferation, metastasis and inhibited apoptosis in vitro. In vivo, LINC00152 overexpression significantly promoted tumor growth. Mechanistic analyses indicated that LINC00152 could participate in the phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway, and transcription factor specificity protein 1 (SP1) induces its overexpression. |
Pubmed ID | 27829993 |
Year | 2016 |
Title | Upregulation of long non-coding RNA LINC00152 by SP1 contributes to gallbladder cancer cell growth and tumor metastasis via PI3K/AKT pathway. |
External Links
Links for LINC00152 | GenBank HGNC NONCODE |
Links for gallbladder cancer | OMIM COSMIC |