| Enhancer ID: | E_01_0520 |
| Species: | human |
| Position : | chr17:28503593-28505593 |
| Biosample name: | |
| Experiment class : | High+Lowthroughput |
| Enhancer type: | Enhancer |
| Disease: | Non small cell lung cancer (nsclc) |
| Pubmed ID: | 29725441 |
| Enhancer experiment: | Transfection,Western blot,RNA extraction,RT?qPCR,Invasion assay,MTT,Quantitative chromatin immunoprecipitation (qChIP),Dual?luciferase reporter assay, |
| Enhancer experiment description: | In conclusion, the present study demonstrated that FOXN1 served major roles in NSCLC proliferation and invasion by directly repressing EZH2 and ?-catenin, which suggested that FOXN1 may function as a tumor suppressor in NSCLC. |
| Target gene : | FOXN1 |
| Strong evidence: | qRT-PCR,qPCR,ChIP,3C |
| Less strong evidence: | RNA-Seq |
| Target gene experiment description: | In conclusion, the present study demonstrated that FOXN1 served major roles in NSCLC proliferation and invasion by directly repressing EZH2 and ?-catenin, which suggested that FOXN1 may function as a tumor suppressor in NSCLC.;In conclusion, the present study demonstrated that FOXN1 served major roles in NSCLC proliferation and invasion by directly repressing EZH2 and ?-catenin, which suggested that FOXN1 may function as a tumor suppressor in NSCLC. |
| TF name : | EZH2(ENX-1,ENX1b,KMT6,KMT6A,WVS,WVS2,EZH2) |
| TF experiment: | Transfection,Western blot,RNA extraction,RT?qPCR,Invasion assay,MTT,Quantitative chromatin immunoprecipitation (qChIP),Dual?luciferase reporter assay, |
| TF experiment description: | In conclusion, the present study demonstrated that FOXN1 served major roles in NSCLC proliferation and invasion by directly repressing EZH2 and ?-catenin, which suggested that FOXN1 may function as a tumor suppressor in NSCLC.;In conclusion, the present study demonstrated that FOXN1 served major roles in NSCLC proliferation and invasion by directly repressing EZH2 and ?-catenin, which suggested that FOXN1 may function as a tumor suppressor in NSCLC. |
| Enhancer function : | In conclusion, the present study demonstrated that FOXN1 served major roles in NSCLC proliferation and invasion by directly repressing EZH2 and ?-catenin, which suggested that FOXN1 may function as a tumor suppressor in NSCLC. |
| Enhancer function experiment: | Immunohistochemical staining |
| Enhancer function experiment description: |
In conclusion, the present study demonstrated that FOXN1 served major roles in NSCLC proliferation and invasion by directly repressing EZH2 and ?-catenin, which suggested that FOXN1 may function as a tumor suppressor in NSCLC. |
| SNP ID: | -- |
| GeneName | Pathway Name | Source | Gene Number |
|---|---|---|---|
| EZH2 | Activation of anterior HOX genes in hindbrain development during early embryogenesis | reactome | 120 |
| EZH2 | Oxidative Stress Induced Senescence | reactome | 120 |
| EZH2 | PKMTs methylate histone lysines | reactome | 64 |
| EZH2 | PRC2 methylates histones and DNA | reactome | 71 |
| EZH2 | Hs_Endoderm_Differentiation_WP2853_88152 | wikipathways | 62 |
| EZH2 | Hs_Interactome_of_polycomb_repressive_complex_2_(PRC2)_WP2916_88672 | wikipathways | 15 |