Basic Information
LncRNA/CircRNA Name | LIMT |
Synonyms | NA |
Region | GRCh38_12:121795267-121803906 |
Ensemble | ENSG00000212694 |
Refseq | NR_002809 |
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 | epithelial ovarian cancer |
ICD-0-3 | C56.9 |
Methods | qRT-PCR, Western blotting etc. |
Sample | The human monocyte cell line THP-1 (ATCC, USA) |
Expression Pattern | down-regulated |
Function Description | THP-1 cells exhibited the phenotype markers of M2-like TAMs with low proportion of CD14+ marker and high proportion of CD68+, CD204+, CD206+ markers within the application of PMA. After co-culturing with M2-like TAMs, EGF concentration in the supernatants was significantly increased in a time-dependent manner. Besides, OC cells presented better cell viability, higher cell proliferation, and stronger migration and invasion. The expression of EMT-related markers N-cadherin, Vimentin and EGFR/ERK signals were markedly up-regulated, while E-cadherin was significantly decreased. However, these effects induced by co-culture system were reversed by the application of AG1478 (an EGFR inhibitor) or LIMT overexpression. Furthermore, the endogenous expression of LIMT was decreased in OC cell lines compared with the control group. Also, the in vivo experiments verified that the inhibition of EGFR signaling by AG1478 or overexpression of LIMT effectively repressed the tumor growth. |
Pubmed ID | 31062668 |
Year | 2019 |
Title | M2-like tumor-associated macrophages-secreted EGF promotes epithelial ovarian cancer metastasis via activating EGFR-ERK signaling and suppressing lncRNA LIMT expression |
External Links
Links for LIMT | GenBank HGNC NONCODE |
Links for epithelial ovarian cancer | OMIM COSMIC |