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©The Author(s) 2024.
World J Stem Cells. Feb 26, 2024; 16(2): 207-227
Published online Feb 26, 2024. doi: 10.4252/wjsc.v16.i2.207
Published online Feb 26, 2024. doi: 10.4252/wjsc.v16.i2.207
Figure 5 VX-509 downregulates Nodal and its downstream protein p-Smad2/3 in colorectal cancer-derived cancer stem cells.
A: Volcano plot of differentially expressed genes in the HT29 cancer stem cells (CSCs) Mock and VX-509-treated groups; B: Gene Ontology enrichment image of the differentially expressed genes; C: Nodal mRNA expression levels in the colorectal cancer (CRC)-derived CSCs Mock and VX-509-treated group; D-F: Protein expression levels of Nodal, p-Smad2/3 (D) and JAK3 (F) in CRC-derived CSCs treated with different concentrations of VX-509 (E). Densitometric analysis of Nodal and p-Smad2/3, normalized against GAPDH. n = 3. aP < 0.05, bP < 0.01, cP < 0.001, dP < 0.0001 compared to the HCT116 cancer stem cells Mock group and HT29 cancer stem cells Mock group. CSC: Cancer stem cell; DEG: Differentially expressed gene.
- Citation: Yuan Y, Zhang XF, Li YC, Chen HQ, Wen T, Zheng JL, Zhao ZY, Hu QY. VX-509 attenuates the stemness characteristics of colorectal cancer stem-like cells by regulating the epithelial-mesenchymal transition through Nodal/Smad2/3 signaling. World J Stem Cells 2024; 16(2): 207-227
- URL: https://www.wjgnet.com/1948-0210/full/v16/i2/207.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v16.i2.207