Basic Information
LncRNA/CircRNA Name | LINC00511 |
Synonyms | LINC00511, LCAL5, onco-lncRNA-12 |
Region | GRCh38_17:72323123-72640472 |
Ensemble | ENSG00000227036 |
Refseq | NR_033876 |
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 | lung cancer |
ICD-0-3 | C34 |
Methods | qPCR, Western blot, RNAi, other |
Sample | lung cancer cell lines |
Expression Pattern | down-regulated |
Function Description | Western blot results showed that silencing LINC00511 inhibited epithelial-mesenchymal transition (EMT), which resulted in decreased expression levels of ZEB2, N-cadherin, and vimentin and increased expression levels of E-cadherin. Additionally, silencing LINC00511 significantly upregulated PTEN mRNA and protein expression, increased FOXO1, and inactivated AKT. Furthermore, we found that PTEN knockdown reversed the inhibition of cell migration and proliferation induced by LINC00511 siRNA, markedly reduced p-FOXO1 expression, and promoted p-AKT expression and EMT in A549 and H460 cells. Therefore, these findings revealed that LINC00511 functions as an oncogene through the PTEN-AKT-FOXO1 signaling pathway in lung cancer, providing a potential target of metastasis in lung cancer. |
Pubmed ID | 31415720 |
Year | 2019 |
Title | Silencing LINC00511 Inhibits Cell Proliferation, Migration, and Epithelial-Mesenchymal Transition via the PTEN-AKT-FOXO1 Signaling Pathway in Lung Cancer |
External Links
Links for LINC00511 | GenBank HGNC NONCODE |
Links for lung cancer | OMIM COSMIC |