human liver cancer cells Search Results


93
Celprogen Inc liver cancer stem cells lcscs
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Liver Cancer Stem Cells Lcscs, supplied by Celprogen Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Celprogen Inc human liver cancer cell line
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Human Liver Cancer Cell Line, supplied by Celprogen Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
human liver cancer cell line - by Bioz Stars, 2026-03
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90
Procell Inc human liver cancer cell line 7,721
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Human Liver Cancer Cell Line 7,721, supplied by Procell Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Broad Institute Inc rna-seq data of different human liver cancer cell lines
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Rna Seq Data Of Different Human Liver Cancer Cell Lines, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rna-seq data of different human liver cancer cell lines/product/Broad Institute Inc
Average 90 stars, based on 1 article reviews
rna-seq data of different human liver cancer cell lines - by Bioz Stars, 2026-03
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90
Korean Cell Line Bank human liver cancer cell lines huh-7 (mutant tp53)
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Human Liver Cancer Cell Lines Huh 7 (Mutant Tp53), supplied by Korean Cell Line Bank, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Tokiwa Inc liver cell biology
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Liver Cell Biology, supplied by Tokiwa Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
liver cell biology - by Bioz Stars, 2026-03
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90
SuperBioChips human tissue arrays containing hcc cells and corresponding adjacent non-cancerous liver tissues csa4
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Human Tissue Arrays Containing Hcc Cells And Corresponding Adjacent Non Cancerous Liver Tissues Csa4, supplied by SuperBioChips, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human tissue arrays containing hcc cells and corresponding adjacent non-cancerous liver tissues csa4/product/SuperBioChips
Average 90 stars, based on 1 article reviews
human tissue arrays containing hcc cells and corresponding adjacent non-cancerous liver tissues csa4 - by Bioz Stars, 2026-03
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90
China Center for Type Culture Collection snu387 human liver cancer cell line
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Snu387 Human Liver Cancer Cell Line, supplied by China Center for Type Culture Collection, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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90
Pasteur Institute lcl-pi 11 cells
Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in <t>normal</t> <t>hepatocytes</t> and <t>LCSCs</t> under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).
Lcl Pi 11 Cells, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Fuxiang Biotechnology Co Ltd human liver cancer mhcc97 cell line
Isolation and characterization of liver cancer stem cells derived from the <t>MHCC97</t> cell line. A: Flow cytometry analysis of CD133 expression following sorting. CD133+ cells from MHCC97 cells formed liver cancer spheroids in stem cell-conditioned medium (200 × magnification); B: Anchorage-dependent growth of MHCC97 cells, tumor spheroid formed by CD133+ cells, tumor spheroid formed by parental MHCC97 cells; C: Secondary tumorspheres formed by single cells from dissociated primary liver spheroids (400 × magnification); D: Expression of stem cell surface markers CD44 and CD133 in CD133+ sphere-forming cells (SFCs) and parental cells; E: Hematoxylin-eosin staining revealed similar histological characteristics in tumor xenografts derived from CD133+ SFCs and their parental cells (100 × magnification).
Human Liver Cancer Mhcc97 Cell Line, supplied by Fuxiang Biotechnology Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human liver cancer mhcc97 cell line/product/Fuxiang Biotechnology Co Ltd
Average 90 stars, based on 1 article reviews
human liver cancer mhcc97 cell line - by Bioz Stars, 2026-03
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Beyotime human liver cancer cell lines mhcc97l
Isolation and characterization of liver cancer stem cells derived from the <t>MHCC97</t> cell line. A: Flow cytometry analysis of CD133 expression following sorting. CD133+ cells from MHCC97 cells formed liver cancer spheroids in stem cell-conditioned medium (200 × magnification); B: Anchorage-dependent growth of MHCC97 cells, tumor spheroid formed by CD133+ cells, tumor spheroid formed by parental MHCC97 cells; C: Secondary tumorspheres formed by single cells from dissociated primary liver spheroids (400 × magnification); D: Expression of stem cell surface markers CD44 and CD133 in CD133+ sphere-forming cells (SFCs) and parental cells; E: Hematoxylin-eosin staining revealed similar histological characteristics in tumor xenografts derived from CD133+ SFCs and their parental cells (100 × magnification).
Human Liver Cancer Cell Lines Mhcc97l, supplied by Beyotime, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
human liver cancer cell lines mhcc97l - by Bioz Stars, 2026-03
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90
Asterand Inc human liver cancer hepg2 cell line
Isolation and characterization of liver cancer stem cells derived from the <t>MHCC97</t> cell line. A: Flow cytometry analysis of CD133 expression following sorting. CD133+ cells from MHCC97 cells formed liver cancer spheroids in stem cell-conditioned medium (200 × magnification); B: Anchorage-dependent growth of MHCC97 cells, tumor spheroid formed by CD133+ cells, tumor spheroid formed by parental MHCC97 cells; C: Secondary tumorspheres formed by single cells from dissociated primary liver spheroids (400 × magnification); D: Expression of stem cell surface markers CD44 and CD133 in CD133+ sphere-forming cells (SFCs) and parental cells; E: Hematoxylin-eosin staining revealed similar histological characteristics in tumor xenografts derived from CD133+ SFCs and their parental cells (100 × magnification).
Human Liver Cancer Hepg2 Cell Line, supplied by Asterand Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in normal hepatocytes and LCSCs under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).

Journal: International Journal of Molecular Sciences

Article Title: MicroRNA Profiling of PRELI-Modulated Exosomes and Effects on Hepatic Cancer Stem Cells

doi: 10.3390/ijms252413299

Figure Lengend Snippet: Levels of AKT signaling molecules (phosphorylated AKT and phosphorylated mTORC1) in normal hepatocytes and LCSCs under various exosomes. (CE: control cellular exosome, UPE: upregulated PRELI cellular exosome, DPEs: downregulated PRELI cellular exosome) (* p < 0.05, ** p < 0.01,*** p < 0.001).

Article Snippet: Liver cancer stem cells (LCSCs) (sku: 36116-43; Celprogen, Torrance, CA, USA) and normal hepatocytes (NHs) (THLE-3; ATCC, Manassas, VA, USA) were cultured with Human Liver Cancer Stem Cell Media (Celprogen) and BEGM (Bronchial Epithelial Cell Growth Medium) (Lonza, Workingham, UK) using BEGM Bullet Kits (Lonza) at 37 °C, 5% CO 2 .

Techniques: Control

Isolation and characterization of liver cancer stem cells derived from the MHCC97 cell line. A: Flow cytometry analysis of CD133 expression following sorting. CD133+ cells from MHCC97 cells formed liver cancer spheroids in stem cell-conditioned medium (200 × magnification); B: Anchorage-dependent growth of MHCC97 cells, tumor spheroid formed by CD133+ cells, tumor spheroid formed by parental MHCC97 cells; C: Secondary tumorspheres formed by single cells from dissociated primary liver spheroids (400 × magnification); D: Expression of stem cell surface markers CD44 and CD133 in CD133+ sphere-forming cells (SFCs) and parental cells; E: Hematoxylin-eosin staining revealed similar histological characteristics in tumor xenografts derived from CD133+ SFCs and their parental cells (100 × magnification).

Journal: World Journal of Gastroenterology : WJG

Article Title: 8-bromo-7-methoxychrysin inhibits properties of liver cancer stem cells via downregulation of ?-catenin

doi: 10.3748/wjg.v19.i43.7680

Figure Lengend Snippet: Isolation and characterization of liver cancer stem cells derived from the MHCC97 cell line. A: Flow cytometry analysis of CD133 expression following sorting. CD133+ cells from MHCC97 cells formed liver cancer spheroids in stem cell-conditioned medium (200 × magnification); B: Anchorage-dependent growth of MHCC97 cells, tumor spheroid formed by CD133+ cells, tumor spheroid formed by parental MHCC97 cells; C: Secondary tumorspheres formed by single cells from dissociated primary liver spheroids (400 × magnification); D: Expression of stem cell surface markers CD44 and CD133 in CD133+ sphere-forming cells (SFCs) and parental cells; E: Hematoxylin-eosin staining revealed similar histological characteristics in tumor xenografts derived from CD133+ SFCs and their parental cells (100 × magnification).

Article Snippet: The human liver cancer MHCC97 cell line was purchased from Fuxiang Biotechnology Co., Ltd. (Shanghai, China).

Techniques: Isolation, Derivative Assay, Flow Cytometry, Expressing, Staining

Tumorsphere formation ability of CD133 + cells derived from the  MHCC97  cell line (mean ± SD, n = 3)

Journal: World Journal of Gastroenterology : WJG

Article Title: 8-bromo-7-methoxychrysin inhibits properties of liver cancer stem cells via downregulation of ?-catenin

doi: 10.3748/wjg.v19.i43.7680

Figure Lengend Snippet: Tumorsphere formation ability of CD133 + cells derived from the MHCC97 cell line (mean ± SD, n = 3)

Article Snippet: The human liver cancer MHCC97 cell line was purchased from Fuxiang Biotechnology Co., Ltd. (Shanghai, China).

Techniques: Derivative Assay

Tumorigenicity of CD133 + sphere forming cell derived from  MHCC97  cells in Balb/c-nu mice

Journal: World Journal of Gastroenterology : WJG

Article Title: 8-bromo-7-methoxychrysin inhibits properties of liver cancer stem cells via downregulation of ?-catenin

doi: 10.3748/wjg.v19.i43.7680

Figure Lengend Snippet: Tumorigenicity of CD133 + sphere forming cell derived from MHCC97 cells in Balb/c-nu mice

Article Snippet: The human liver cancer MHCC97 cell line was purchased from Fuxiang Biotechnology Co., Ltd. (Shanghai, China).

Techniques: Derivative Assay

Effects of 8-bromo-7-methoxychrysin on cell proliferation and self-renewal. 8-bromo-7-methoxychrysin (BrMC) inhibited proliferation (A), self-renewal (B and C) of liver cancer stem cells derived from MHCC97 cell line (mean ± SD, n = 3). aP < 0.05 vs unsorted MHCC97 cells treated with corresponding concentrations of BrMC. cP < 0.05 vs corresponding 0.1% DMSO treated group. Tumor sphere morphology is shown as the phase contrast image (400 × magnification).

Journal: World Journal of Gastroenterology : WJG

Article Title: 8-bromo-7-methoxychrysin inhibits properties of liver cancer stem cells via downregulation of ?-catenin

doi: 10.3748/wjg.v19.i43.7680

Figure Lengend Snippet: Effects of 8-bromo-7-methoxychrysin on cell proliferation and self-renewal. 8-bromo-7-methoxychrysin (BrMC) inhibited proliferation (A), self-renewal (B and C) of liver cancer stem cells derived from MHCC97 cell line (mean ± SD, n = 3). aP < 0.05 vs unsorted MHCC97 cells treated with corresponding concentrations of BrMC. cP < 0.05 vs corresponding 0.1% DMSO treated group. Tumor sphere morphology is shown as the phase contrast image (400 × magnification).

Article Snippet: The human liver cancer MHCC97 cell line was purchased from Fuxiang Biotechnology Co., Ltd. (Shanghai, China).

Techniques: Derivative Assay

8-bromo-7-methoxychrysin inhibition of liver cancer stem cells. 8-bromo-7-methoxychrysin (BrMC) inhibited epithelial-mesenchymal transition (EMT, A and B) and invasion (C and D) of liver cancer stem cells derived from the MHCC97 cell line (mean ± SD, n = 3). Cell morphological changes associated with EMT are shown as the phase contrast image (200 × magnification). aP < 0.05 vs unsorted MHCC97 cells treated with corresponding concentrations of BrMC, cP < 0.05 vs corresponding 0.1% DMSO treated group.

Journal: World Journal of Gastroenterology : WJG

Article Title: 8-bromo-7-methoxychrysin inhibits properties of liver cancer stem cells via downregulation of ?-catenin

doi: 10.3748/wjg.v19.i43.7680

Figure Lengend Snippet: 8-bromo-7-methoxychrysin inhibition of liver cancer stem cells. 8-bromo-7-methoxychrysin (BrMC) inhibited epithelial-mesenchymal transition (EMT, A and B) and invasion (C and D) of liver cancer stem cells derived from the MHCC97 cell line (mean ± SD, n = 3). Cell morphological changes associated with EMT are shown as the phase contrast image (200 × magnification). aP < 0.05 vs unsorted MHCC97 cells treated with corresponding concentrations of BrMC, cP < 0.05 vs corresponding 0.1% DMSO treated group.

Article Snippet: The human liver cancer MHCC97 cell line was purchased from Fuxiang Biotechnology Co., Ltd. (Shanghai, China).

Techniques: Inhibition, Derivative Assay

8-bromo-7-methoxychrysin eliminated liver cancer stem cells derived from MHCC97 cell line in vivo. Effects of 8-bromo-7-methoxychrysin (BrMC) on growth of primary and secondary tumor xenografts derived from liver cancer stem cells (LCSCs) (A and B, mean ± SD, n = 12). aP < 0.05 vs refined olive oil treatment model, cP < 0.05 vs treatment with 12.5 mg/kg BrMC. Immunohistochemical analysis of CD44 and CD133 in LCSC-derived tumors before and after BrMC treatment (C and D).

Journal: World Journal of Gastroenterology : WJG

Article Title: 8-bromo-7-methoxychrysin inhibits properties of liver cancer stem cells via downregulation of ?-catenin

doi: 10.3748/wjg.v19.i43.7680

Figure Lengend Snippet: 8-bromo-7-methoxychrysin eliminated liver cancer stem cells derived from MHCC97 cell line in vivo. Effects of 8-bromo-7-methoxychrysin (BrMC) on growth of primary and secondary tumor xenografts derived from liver cancer stem cells (LCSCs) (A and B, mean ± SD, n = 12). aP < 0.05 vs refined olive oil treatment model, cP < 0.05 vs treatment with 12.5 mg/kg BrMC. Immunohistochemical analysis of CD44 and CD133 in LCSC-derived tumors before and after BrMC treatment (C and D).

Article Snippet: The human liver cancer MHCC97 cell line was purchased from Fuxiang Biotechnology Co., Ltd. (Shanghai, China).

Techniques: Derivative Assay, In Vivo, Immunohistochemical staining

β-catenin siRNA synergized the inhibitory effects of 8-bromo-7-methoxychrysin. 8-bromo-7-methoxychrysin (BrMC) downregulated CD44 and CD133 expression in liver cancer stem cells in a concentration-dependent manner (A). β-catenin was highly expressed in CD133+ sphere forming cells (SFCs) and was downregulated by BrMC treatment (B). β-catenin siRNA decreased the protein level of β-catenin (C) and stem cell markers (E), and significantly inhibited self-renewal capacity (D) of CD133+ SFCs (mean ± SD, n = 3). aP < 0.05 vs CD133+ SFCs or control siRNA transfected CD133+ SFCs. BrMC enhanced β-catenin siRNA induced downregulation of β-catenin expression (F) and inhibition of self-renewal capacity (G) in CD133+ SFCs (mean ± SD, n = 3). aP < 0.05 vs CD133+ SFCs derived from the MHCC97 cell line. cP < 0.05 vs 0.1 μmol/L BrMC or β-catenin siRNA treated CD133+ SFCs.

Journal: World Journal of Gastroenterology : WJG

Article Title: 8-bromo-7-methoxychrysin inhibits properties of liver cancer stem cells via downregulation of ?-catenin

doi: 10.3748/wjg.v19.i43.7680

Figure Lengend Snippet: β-catenin siRNA synergized the inhibitory effects of 8-bromo-7-methoxychrysin. 8-bromo-7-methoxychrysin (BrMC) downregulated CD44 and CD133 expression in liver cancer stem cells in a concentration-dependent manner (A). β-catenin was highly expressed in CD133+ sphere forming cells (SFCs) and was downregulated by BrMC treatment (B). β-catenin siRNA decreased the protein level of β-catenin (C) and stem cell markers (E), and significantly inhibited self-renewal capacity (D) of CD133+ SFCs (mean ± SD, n = 3). aP < 0.05 vs CD133+ SFCs or control siRNA transfected CD133+ SFCs. BrMC enhanced β-catenin siRNA induced downregulation of β-catenin expression (F) and inhibition of self-renewal capacity (G) in CD133+ SFCs (mean ± SD, n = 3). aP < 0.05 vs CD133+ SFCs derived from the MHCC97 cell line. cP < 0.05 vs 0.1 μmol/L BrMC or β-catenin siRNA treated CD133+ SFCs.

Article Snippet: The human liver cancer MHCC97 cell line was purchased from Fuxiang Biotechnology Co., Ltd. (Shanghai, China).

Techniques: Expressing, Concentration Assay, Control, Transfection, Inhibition, Derivative Assay

Wnt3a treatment antagonized the inhibitory effects of 8-bromo-7-methoxychrysin. Wnt3a treatment resulted in an increase in the expression of β-catenin in both liver cancer stem cells (LCSCs) and parental MHCC97 cells (A) and attenuated the effects of 8-bromo-7-methoxychrysin (BrMC) on the expression of β-catenin (B) and stem cell markers (C), and self-renewal capacity (D) of LCSCs derived from the MHCC97 cell line. aP < 0.05 vs CD133+ SFCs, c P < 0.05 vs 0.1 μmol/L BrMC or Wnt 3a alone treated group.

Journal: World Journal of Gastroenterology : WJG

Article Title: 8-bromo-7-methoxychrysin inhibits properties of liver cancer stem cells via downregulation of ?-catenin

doi: 10.3748/wjg.v19.i43.7680

Figure Lengend Snippet: Wnt3a treatment antagonized the inhibitory effects of 8-bromo-7-methoxychrysin. Wnt3a treatment resulted in an increase in the expression of β-catenin in both liver cancer stem cells (LCSCs) and parental MHCC97 cells (A) and attenuated the effects of 8-bromo-7-methoxychrysin (BrMC) on the expression of β-catenin (B) and stem cell markers (C), and self-renewal capacity (D) of LCSCs derived from the MHCC97 cell line. aP < 0.05 vs CD133+ SFCs, c P < 0.05 vs 0.1 μmol/L BrMC or Wnt 3a alone treated group.

Article Snippet: The human liver cancer MHCC97 cell line was purchased from Fuxiang Biotechnology Co., Ltd. (Shanghai, China).

Techniques: Expressing, Derivative Assay