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Image Search Results
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Article Title: ALDH1A1 maintains the cancer stem-like cells properties of esophageal squamous cell carcinoma by activating the AKT signal pathway and interacting with β-catenin.
doi: 10.1016/j.biopha.2020.109940
Figure Lengend Snippet: Fig. 1. Differential expression of ALDH1A1 protein in ESCC tissues and the lost ALDH1A1 expression associated with poor overall survival. IHC analysis of ALDH1A1 expression in ESCC tissues. (A) Low expression of ALDH1A1 protein in hyperplastic esophagus tissues. (B, C) Low expression of ALDH1A1 protein in ESCC. (D) High expression of ALDH1A1 protein in ESCC. Scale bar =100 μm. (E) Overall survival of ESCC patients stratified in accordance with ALDH1A1 protein expression.
Article Snippet: The primary antibodies were incubated at 4 °C overnight: anti-AKT (dilution 1:1000), anti-AKT1 (1:1000), p-AKT (Ser473) (1:1000), p-AKT (Thr308) (1:1000) and Vimentin (1:500) were purchased from CST, βcatenin (1:2000), c-Myc (1:1000) from
Techniques: Quantitative Proteomics, Expressing
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Article Title: ALDH1A1 maintains the cancer stem-like cells properties of esophageal squamous cell carcinoma by activating the AKT signal pathway and interacting with β-catenin.
doi: 10.1016/j.biopha.2020.109940
Figure Lengend Snippet: Fig. 2. Ectopic expression of ALDH1A1 promoted spherogenesis and colony formation of ESCC cells in vitro. (A) Tumor sphere formation assays in KYSE-510/NC, KYSE-510/ALDH1A1, KYSE-150/NC, and KYSE-150/ALDH1A1 cells. Scale bar =200 μm. (B) Spherogenesis rate. The graph is the summarized data of three in- dependent experiments, ***P < 0.001. (C) ALDH1A1 expression promoted colony formation of KYSE-150 cells. The graph is the summarized data of three in- dependent experiments, ***P < 0.001. (D) Cell survival assay showed that ALDH1A1 expression promoted TE-1 cell resistance to 5-Fu. *P < 0.05, **P < 0.01, ***P < 0.001.
Article Snippet: The primary antibodies were incubated at 4 °C overnight: anti-AKT (dilution 1:1000), anti-AKT1 (1:1000), p-AKT (Ser473) (1:1000), p-AKT (Thr308) (1:1000) and Vimentin (1:500) were purchased from CST, βcatenin (1:2000), c-Myc (1:1000) from
Techniques: Expressing, In Vitro, Clonogenic Cell Survival Assay
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Article Title: ALDH1A1 maintains the cancer stem-like cells properties of esophageal squamous cell carcinoma by activating the AKT signal pathway and interacting with β-catenin.
doi: 10.1016/j.biopha.2020.109940
Figure Lengend Snippet: Fig. 3. Ectopic expression of ALDH1A1 promoted tumor initiation in vivo. (A) Equal KYSE-150/NC and KYSE-150/ALDH1A1 cells were injected into different axillaries (white arrow) of six BALB/c nude mice. (B) Transplanted tumor for- mation numbers.
Article Snippet: The primary antibodies were incubated at 4 °C overnight: anti-AKT (dilution 1:1000), anti-AKT1 (1:1000), p-AKT (Ser473) (1:1000), p-AKT (Thr308) (1:1000) and Vimentin (1:500) were purchased from CST, βcatenin (1:2000), c-Myc (1:1000) from
Techniques: Expressing, In Vivo, Injection
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Article Title: ALDH1A1 maintains the cancer stem-like cells properties of esophageal squamous cell carcinoma by activating the AKT signal pathway and interacting with β-catenin.
doi: 10.1016/j.biopha.2020.109940
Figure Lengend Snippet: Fig. 4. ALDH1A1 expression regulated AKT and β-catenin expressions. (A) RT-qPCR assay detected mRNA expression levels of ALDH1A1, AKT1, β-catenin, Slug, c-Myc, and Vimentin in KYSE-150 and TE-1 cells. ** P < 0.01; *** P < 0.001; ns, not significant. (B, C) Western blot assay showed the ALDH1A1, p-AKT, total-AKT1, β-catenin, c-Myc, and β-actin protein expressions after NCT501 treatment or ALDH1A1 overexpression in ESCC cells, *: GAPDH. D, Western blot assay showed the ALDH1A1, AKT1, β-catenin, and β-actin expression levels after MK-2206 or NCT501 treatment. (E) Western blot gray scale for the relative protein levels of Fig. 4E. ***: P < 0.001.
Article Snippet: The primary antibodies were incubated at 4 °C overnight: anti-AKT (dilution 1:1000), anti-AKT1 (1:1000), p-AKT (Ser473) (1:1000), p-AKT (Thr308) (1:1000) and Vimentin (1:500) were purchased from CST, βcatenin (1:2000), c-Myc (1:1000) from
Techniques: Expressing, Quantitative RT-PCR, Western Blot, Over Expression
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Article Title: ALDH1A1 maintains the cancer stem-like cells properties of esophageal squamous cell carcinoma by activating the AKT signal pathway and interacting with β-catenin.
doi: 10.1016/j.biopha.2020.109940
Figure Lengend Snippet: Fig. 5. ALDH1A1 interacted with β-catenin. Co-localization of ALDH1A1 and β-catenin in (A) adherent cells (Scale bar =20 μm) and (B) stem cell spheres (Scale bar =50 μm) of KYSE-510. Images were collected by a confocal microscope. (C) Co-IP, Western blot assay to detect the interaction of ALDH1A1 and β-catenin. (D) Western blot to detect β-catenin protein levels after cycloheximide (CHX) treatment. (E) Western blot to detect ALDH1A1and β-catenin protein expression in cytoplasm and nuclear of adherent KYSE-510 cells. (F) TOP/FOP flash activity assay revealed that ALDH1A1 promoted wnt/β-catenin activity in KYSE-293 T cells.
Article Snippet: The primary antibodies were incubated at 4 °C overnight: anti-AKT (dilution 1:1000), anti-AKT1 (1:1000), p-AKT (Ser473) (1:1000), p-AKT (Thr308) (1:1000) and Vimentin (1:500) were purchased from CST, βcatenin (1:2000), c-Myc (1:1000) from
Techniques: Microscopy, Co-Immunoprecipitation Assay, Western Blot, Expressing, Activity Assay