Journal of Cellular and Molecular Medicine · 2019 · 49 citations · 31 references
Life SciencesCell BiologyOncologyCell SignalingMolecular OncologyStem Cell BiologyCancer Stem Cell BiologyCancer Stem Cell MaintenanceCancer Stem CellsEpithelial-mesenchymal TransitionStem Cell DifferentiationStem Cell TumorigenicityCancer Stem Cell Signaling PathwaysCancer Stem Cell TraitsEpithelial TransitionMesenchymal TransitionSpheroid CultureStemness RegulationStemness Signaling PathwaysTumor Stem Cell Differentiation
Abstract Krüppel‐like factor 4 (KLF4) was closely associated with epithelial‐mesenchymal transition and stemness in colorectal cancer stem cells (CSCs)‐enriched spheroid cells. Nonetheless, the underlying molecular mechanism is unclear. This study showed that KLF4 overexpression was accompanied with stemness and mesenchymal features in Lgr5 + CD44 + EpCAM + colorectal CSCs. KLF4 knockdown suppressed stemness, mesenchymal features and activation of the TGF‐β1 pathway, whereas enforced KLF4 overexpression activated TGF‐β1, phosphorylation of Smad 2/3 and Snail expression, and restored stemness and mesenchymal phenotypes. Furthermore, TGF‐β1 pathway inhibition invalidated KLF4‐facilitated stemness and mesenchymal features without affecting KLF4 expression. The data from the current study are the first to demonstrate that KLF4 maintains stemness and mesenchymal properties through the TGF‐β1/Smad/Snail pathway in Lgr5 + CD44 + EpCAM + colorectal CSCs.
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