JIB-04, A Small Molecule Histone Demethylase Inhibitor, Selectively Targets Colorectal Cancer Stem Cells by Inhibiting the Wnt/β-Catenin Signaling Pathway
Autor: | Hye In Cho, Hee Jung Yoon, Yeun Kyu Jang, Ye Hyeon Ahn, Yan Hua Jin, Eun Jung Park, Minseong Kim |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Colorectal cancer Aminopyridines Gene Expression lcsh:Medicine Article 03 medical and health sciences Mice Cancer stem cell In vivo Cell Movement Cell Line Tumor medicine Tumor Cells Cultured Animals Humans Epigenetics Cell Self Renewal lcsh:Science Wnt Signaling Pathway Cell Proliferation Histone Demethylases Multidisciplinary biology Chemistry Cell Cycle lcsh:R Wnt signaling pathway Hydrazones medicine.disease Xenograft Model Antitumor Assays Disease Models Animal 030104 developmental biology biology.protein Cancer research Neoplastic Stem Cells Demethylase lcsh:Q Stem cell Signal transduction Colorectal Neoplasms Biomarkers |
Zdroj: | Scientific Reports, Vol 8, Iss 1, Pp 1-12 (2018) Scientific Reports |
ISSN: | 2045-2322 |
DOI: | 10.1038/s41598-018-24903-0 |
Popis: | Although several epigenetic modulating drugs are suggested to target cancer stem cells (CSCs), additional identification of anti-CSC drugs is still necessary. Here we showed that JIB-04, a pan-selective inhibitor of histone demethylase(s), was identified as a small molecule that selectively target colorectal CSCs. Our data showed that JIB-04 is capable of reducing self-renewal and stemness of colorectal CSCs in three different colorectal cancer cell lines. JIB-04 significantly attenuated CSC tumorsphere formation, growth/relapse, invasion, and migration in vitro. Furthermore, JIB-04-treated colorectal cancer cells showed reduced tumorigenic activity in vivo. RNA sequencing analysis revealed that JIB-04 affected various cancer-related signaling pathways, especially Wnt/β-catenin signaling, which is crucial for the proliferation and maintenance of colorectal cancer cells. qRT-PCR and TOP/FOP flash luciferase assays showed that JIB-04 down-regulated the expression of Wnt/β-catenin-regulated target genes associated with colorectal CSC function. Overall, the effects of JIB-04 were equal to or greater than those of salinomycin, a known anti-colorectal CSC drug, despite the lower concentration of JIB-04 compared with that of salinomycin. Our results strongly suggest that JIB-04 is a promising drug candidate for colorectal cancer therapy. |
Databáze: | OpenAIRE |
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