Enhancer ID: | E_01_0633 |
Species: | human |
Position : | chr4:108044811-108046811 |
Biosample name: | |
Experiment class : | High+Lowthroughput |
Enhancer type: | Enhancer |
Disease: | Colorectal cancer |
Pubmed ID: | 30446587 |
Enhancer experiment: | Luciferase reporter assay, Western blot,immunofluorescence analysis,histopathological analysis ,short tandem repeat profiling analysis, cell proliferation assay, MTT assay,FACS analysis |
Enhancer experiment description: | Niclosamide blocks the transcription of DCLK1-B by interrupting the binding of LEF1 to DCLK1-B promoter. DCLK1-B depletion impairs cancer stemness resulting in reduced survival potential and increased apoptosis, thus sensitizing CRC to chemoradiation. |
Target gene : | -- |
Strong evidence: | qRT-PCR,qPCR,ChIP,3C |
Less strong evidence: | RNA-Seq |
Target gene experiment description: | Niclosamide blocks the transcription of DCLK1-B by interrupting the binding of LEF1 to DCLK1-B promoter. DCLK1-B depletion impairs cancer stemness resulting in reduced survival potential and increased apoptosis, thus sensitizing CRC to chemoradiation. |
TF name : | LEF1(LEF-1,TCF10,TCF1ALPHA,TCF7L3) |
TF experiment: | Luciferase reporter assay, Western blot,immunofluorescence analysis,histopathological analysis ,short tandem repeat profiling analysis, cell proliferation assay, MTT assay,FACS analysis |
TF experiment description: | Niclosamide blocks the transcription of DCLK1-B by interrupting the binding of LEF1 to DCLK1-B promoter. DCLK1-B depletion impairs cancer stemness resulting in reduced survival potential and increased apoptosis, thus sensitizing CRC to chemoradiation. |
Enhancer function : | Niclosamide blocks the transcription of DCLK1-B by interrupting the binding of LEF1 to DCLK1-B promoter. DCLK1-B depletion impairs cancer stemness resulting in reduced survival potential and increased apoptosis, thus sensitizing CRC to chemoradiation. |
Enhancer function experiment: | Immunohistochemical staining |
Enhancer function experiment description: |
Niclosamide blocks the transcription of DCLK1-B by interrupting the binding of LEF1 to DCLK1-B promoter. DCLK1-B depletion impairs cancer stemness resulting in reduced survival potential and increased apoptosis, thus sensitizing CRC to chemoradiation. |
SNP ID: | -- |