Basic Information
LncRNA/CircRNA Name | TUBA4B |
Synonyms | TUBA4B, TUBA4 |
Region | GRCh38_2:219253243-219272188 |
Ensemble | ENSG00000243910 |
Refseq | NA |
Classification Information
Regulatory Mechanism | Biological Function | Clinical Application | |||
---|---|---|---|---|---|
TF | Immune | Survival | |||
Enhancer | Apoptosis | apoptosis | Drug | ||
Variant | Cell Growth | Circulating | |||
MiRNA | EMT | Metastasis | |||
Methylation | Coding Ability | Recurrence |
Cancer&Entry Information
Cancer Name | gastric cancer |
ICD-0-3 | C16 |
Methods | qPCR, Western blot, Luciferase reporter assay |
Sample | human gastric epithelial GES-1 cells and fve GC cell lines (AGS, SGC-7901, BGC-823, MGC-803 and HGC27), GC and paired normal tissues, blood |
Expression Pattern | down-regulated |
Function Description | TUBA4B was signifcantly decreased in GC tissues, cells and plasma. Low TUBA4B was positively correlated with larger tumor size, lymph node metastasis and advanced TNM stage. Moreover, TUBA4B was identifed as an efective biomarker for the diagnosis and prognosis of patients with GC. Functionally, ectopic expression of TUBA4B inhibited GC cell proliferation, invasion and induced apoptosis in vitro as well as dampened tumor growth and metastasis in vivo. Furthermore, TUBA4B was found to be a competitive endogenous RNA (ceRNA) that could physically bind to and sequester miR-214 and miR-216a/b to increase the expression of their common downstream target PTEN, resulting in inactivation of PI3K/AKT signaling pathway, thereby retarding GC progression. |
Pubmed ID | 31198405 |
Year | 2019 |
Title | LncRNA TUBA4B functions as a competitive endogenous RNA to inhibit gastric cancer progression by elevating PTEN via sponging miR-214 and miR-216a/b |
External Links
Links for TUBA4B | GenBank HGNC NONCODE |
Links for gastric cancer | OMIM COSMIC |