Disease name | Lung Cancer |
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Classfication | Cancer |
Related Enzyme(s) | |
EFO | EFO:0001071 |
DOID | 299 |
OMIM | |
NCI | |
Definition | A carcinoma that has material basis in abnormally proliferating cells, derives from epithelial cells, which originate in glandular tissue. |
Gene symbol | Species | Enzyme | Editing site(s) | Editing Type | PMID | RADAR | REDIportal | Description |
---|---|---|---|---|---|---|---|---|
BLCAP | Human | ADAR1;ADAR2 | 12 | A-to-I | BLCAP-editing level is Decrease in bladder cancer, astrocytomas, colorectal cancer. | |||
NEIL1 | Human | ADAR1 | 1 | A-to-I | ADAR1 gene-amplified lung cancer cell lines show a higher frequency of A-to-I editing in NEIL1 relative to the ADAR1 normal copy number cells. | |||
FAK | Human | ADAR1 | 1 | A-to-I | ADAR posttranscriptionally increased FAK protein abundance by binding to the FAK transcript and edit- ing a specific intronic site that resulted in the increased stabilization of FAK mRNA. Pharmacological inhibition of FAK blocked ADAR-induced invasiveness of LUAD cells, suggesting a potential therapeutic application for LUAD that has a high abundance of ADAR. |
Gene symbol | Disease | Enzyme | Editing Sites | Editing Type | miRBase | PMID | Description |
---|---|---|---|---|---|---|---|
hsa-miR-381 | ADAR2 | 2 | A-to-I | MI0000789 | The A-to-I editing on the proposed targets contributed to the phenotype of lung cancer cells: we found that the overexpression of the edited miR-381 transcripts significantly enhances the growth of tumor cells in comparison with the transfection of the unedited transcripts. |
Enzyme | Full Name | Location | Ensembl | Targets | Related Diseases | Aliases |
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ADAR1 | Adenosine deaminase, RNA specific | Chr1:154582057..154631560 |
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