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 |