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ATCC mouse liver cancer cell line hepa1
GOLM1 expression is upregulated in macrophages and correlates with tumor progression (A) Representative H&E and immunofluorescence microscopy images of carcinoma and para -carcinoma tissue of lung cancer patients. Red, CD68; green, GOLM1; blue, DAPI. Upper row, scale bar = 500 μm; lower row, scale bar = 50 μm. (B) Analyzing the co-localization ratio of CD68 and GOLM1 using Pearson’s correlation coefficients via ImageJ with the JAcop plugin. 10 visual fields from 5 pairs of carcinoma and para -carcinoma tissues were examined. (C) Representative immunofluorescent staining of F4/80 and GOLM1 in liver sections from AAV- Golm1 or AAV-vector infected mice. Scale bar = 100 μm. (D) GOLM1 protein levels in BMDMs derived from AAV- Golm1 or AAV-vector infected mice. (E) Schematic diagram of orthotopic HCC tumor model established by <t>injecting</t> <t>Hepa1-6</t> cells into the liver of AAV- Golm1 or AAV-vector infected mice. (F) Body weight growth curves of mice inoculated with tumor. n = 6 mice per group. (G) Photographs of liver organs with HCC nodules from AAV- Golm1 and AAV-vector mice at terminal growth size. Scale bar = 40 mm. (H) Analysis of the ratio of tumor area to tissue area. n = 6 mice/group. (I) Representative H&E and Ki67 staining images of liver tumor in AAV- Golm1 or AAV-vector infected mice. Red, Ki67; blue, DAPI. Scale bar = 60 μm. (J) Quantitative analysis of the Ki67 positive area. n = 5 mice/group. (K and L) Immunoblotting and statistical graph of the indicated protein levels in tumors of AAV- Golm1 mice and AAV-vector mice. n = 3 mice/group. The data are presented as the means ± SEMs. Statistical significance was determined by two-tailed Student's t test in (B, H, J, and L) and two-way ANOVA followed by Bonferroni's multiple comparisons test (F). ns, not statistically significant. *p < 0.05; **p < 0.01; ***p < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Mouse Liver Cancer Cell Line Hepa1, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GOLM1 expression is upregulated in macrophages and correlates with tumor progression (A) Representative H&E and immunofluorescence microscopy images of carcinoma and para -carcinoma tissue of lung cancer patients. Red, CD68; green, GOLM1; blue, DAPI. Upper row, scale bar = 500 μm; lower row, scale bar = 50 μm. (B) Analyzing the co-localization ratio of CD68 and GOLM1 using Pearson’s correlation coefficients via ImageJ with the JAcop plugin. 10 visual fields from 5 pairs of carcinoma and para -carcinoma tissues were examined. (C) Representative immunofluorescent staining of F4/80 and GOLM1 in liver sections from AAV- Golm1 or AAV-vector infected mice. Scale bar = 100 μm. (D) GOLM1 protein levels in BMDMs derived from AAV- Golm1 or AAV-vector infected mice. (E) Schematic diagram of orthotopic HCC tumor model established by injecting Hepa1-6 cells into the liver of AAV- Golm1 or AAV-vector infected mice. (F) Body weight growth curves of mice inoculated with tumor. n = 6 mice per group. (G) Photographs of liver organs with HCC nodules from AAV- Golm1 and AAV-vector mice at terminal growth size. Scale bar = 40 mm. (H) Analysis of the ratio of tumor area to tissue area. n = 6 mice/group. (I) Representative H&E and Ki67 staining images of liver tumor in AAV- Golm1 or AAV-vector infected mice. Red, Ki67; blue, DAPI. Scale bar = 60 μm. (J) Quantitative analysis of the Ki67 positive area. n = 5 mice/group. (K and L) Immunoblotting and statistical graph of the indicated protein levels in tumors of AAV- Golm1 mice and AAV-vector mice. n = 3 mice/group. The data are presented as the means ± SEMs. Statistical significance was determined by two-tailed Student's t test in (B, H, J, and L) and two-way ANOVA followed by Bonferroni's multiple comparisons test (F). ns, not statistically significant. *p < 0.05; **p < 0.01; ***p < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Journal: Journal of Advanced Research

Article Title: The GOLM1-ACLY pathway regulates macrophage-secreted EFEMP1 via H3K27ac modifications to drive tumor progression

doi: 10.1016/j.jare.2025.07.003

Figure Lengend Snippet: GOLM1 expression is upregulated in macrophages and correlates with tumor progression (A) Representative H&E and immunofluorescence microscopy images of carcinoma and para -carcinoma tissue of lung cancer patients. Red, CD68; green, GOLM1; blue, DAPI. Upper row, scale bar = 500 μm; lower row, scale bar = 50 μm. (B) Analyzing the co-localization ratio of CD68 and GOLM1 using Pearson’s correlation coefficients via ImageJ with the JAcop plugin. 10 visual fields from 5 pairs of carcinoma and para -carcinoma tissues were examined. (C) Representative immunofluorescent staining of F4/80 and GOLM1 in liver sections from AAV- Golm1 or AAV-vector infected mice. Scale bar = 100 μm. (D) GOLM1 protein levels in BMDMs derived from AAV- Golm1 or AAV-vector infected mice. (E) Schematic diagram of orthotopic HCC tumor model established by injecting Hepa1-6 cells into the liver of AAV- Golm1 or AAV-vector infected mice. (F) Body weight growth curves of mice inoculated with tumor. n = 6 mice per group. (G) Photographs of liver organs with HCC nodules from AAV- Golm1 and AAV-vector mice at terminal growth size. Scale bar = 40 mm. (H) Analysis of the ratio of tumor area to tissue area. n = 6 mice/group. (I) Representative H&E and Ki67 staining images of liver tumor in AAV- Golm1 or AAV-vector infected mice. Red, Ki67; blue, DAPI. Scale bar = 60 μm. (J) Quantitative analysis of the Ki67 positive area. n = 5 mice/group. (K and L) Immunoblotting and statistical graph of the indicated protein levels in tumors of AAV- Golm1 mice and AAV-vector mice. n = 3 mice/group. The data are presented as the means ± SEMs. Statistical significance was determined by two-tailed Student's t test in (B, H, J, and L) and two-way ANOVA followed by Bonferroni's multiple comparisons test (F). ns, not statistically significant. *p < 0.05; **p < 0.01; ***p < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Article Snippet: The human HCC cell lines Huh7 and HepG2; the human macrophage lines Thp1and HEK293T and the mouse liver cancer cell line Hepa1-6 were originally obtained from the ATCC.

Techniques: Expressing, Immunofluorescence, Microscopy, Staining, Plasmid Preparation, Infection, Derivative Assay, Western Blot, Two Tailed Test

Macrophage-specific knockout of Golm1 impedes tumor proliferation (A) Schematic representation of orthotopic HCC tumor model established by injecting Hepa1-6 cells into the liver of Golm1 WT or Golm1 MKO mice. (B) Hepa1-6 tumors in Golm1 WT and Golm1 MKO mice at terminal growth size. Scale bar = 40 mm. (C) Analysis of the ratio of tumor area to tissue area. n = 6 mice/group. (D) H&E and Ki67 immunohistochemical staining of liver tumors in Golm1 WT and Golm1 MKO mice. Main image, scale bar = 200 μm; zoomed regions, scale bar = 40 μm. (E) Ki67 positive rate in tumors evaluated by immunohistochemistry analysis. n = 6 fields. (F-G) Representative bands (F) and quantitative analysis (G) of relative protein expression in tumors of Golm1 WT and Golm1 MKO mice. n = 3 mice/group. (H) GSEA enrichment analysis of cancer related pathways based on KEGG. n = 3 mice/group. (I) Schematic representation of the Thp1 nc -Huh7 or Thp1 −/− -Huh7 admixture tumor model on nude mice. (J) Tumor growth curves of subcutaneous models involving Huh7 cells cocultured with Thp1 nc or Thp1 −/− cells. n = 5 nude mice in each group. (K and L) Tumor images (K) and weight (L) of subcutaneous tumor in groups of nude mice. Scale bar = 20 mm. n = 5 nude mice in each group. (M and N) Representative bands (M) and quantitative analysis (N) of relative protein expression in tumors of Huh-7, Thp1 nc -Huh7 or Thp1 −/− -Huh7 nude mice. n = 3 mice/group. The data are presented as the means ± SEMs. Statistical significance was determined by two-tailed Student's t test (C, E, and G) and one-way ANOVA followed by Tukey's multiple comparisons test (J, L, and N). ns, not statistically significant. *p < 0.05; **p < 0.01; ***p < 0.001.

Journal: Journal of Advanced Research

Article Title: The GOLM1-ACLY pathway regulates macrophage-secreted EFEMP1 via H3K27ac modifications to drive tumor progression

doi: 10.1016/j.jare.2025.07.003

Figure Lengend Snippet: Macrophage-specific knockout of Golm1 impedes tumor proliferation (A) Schematic representation of orthotopic HCC tumor model established by injecting Hepa1-6 cells into the liver of Golm1 WT or Golm1 MKO mice. (B) Hepa1-6 tumors in Golm1 WT and Golm1 MKO mice at terminal growth size. Scale bar = 40 mm. (C) Analysis of the ratio of tumor area to tissue area. n = 6 mice/group. (D) H&E and Ki67 immunohistochemical staining of liver tumors in Golm1 WT and Golm1 MKO mice. Main image, scale bar = 200 μm; zoomed regions, scale bar = 40 μm. (E) Ki67 positive rate in tumors evaluated by immunohistochemistry analysis. n = 6 fields. (F-G) Representative bands (F) and quantitative analysis (G) of relative protein expression in tumors of Golm1 WT and Golm1 MKO mice. n = 3 mice/group. (H) GSEA enrichment analysis of cancer related pathways based on KEGG. n = 3 mice/group. (I) Schematic representation of the Thp1 nc -Huh7 or Thp1 −/− -Huh7 admixture tumor model on nude mice. (J) Tumor growth curves of subcutaneous models involving Huh7 cells cocultured with Thp1 nc or Thp1 −/− cells. n = 5 nude mice in each group. (K and L) Tumor images (K) and weight (L) of subcutaneous tumor in groups of nude mice. Scale bar = 20 mm. n = 5 nude mice in each group. (M and N) Representative bands (M) and quantitative analysis (N) of relative protein expression in tumors of Huh-7, Thp1 nc -Huh7 or Thp1 −/− -Huh7 nude mice. n = 3 mice/group. The data are presented as the means ± SEMs. Statistical significance was determined by two-tailed Student's t test (C, E, and G) and one-way ANOVA followed by Tukey's multiple comparisons test (J, L, and N). ns, not statistically significant. *p < 0.05; **p < 0.01; ***p < 0.001.

Article Snippet: The human HCC cell lines Huh7 and HepG2; the human macrophage lines Thp1and HEK293T and the mouse liver cancer cell line Hepa1-6 were originally obtained from the ATCC.

Techniques: Knock-Out, Immunohistochemical staining, Staining, Immunohistochemistry, Expressing, Two Tailed Test