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Epizyme Inc
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Proteintech
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Proteintech
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Journal: International Journal of General Medicine
Article Title: A POSTN + CAF/APOE + TAM Axis is Associated with Tumor Progression and Potential Immunotherapy Resistance in Laryngeal Squamous Cell Carcinoma
doi: 10.2147/IJGM.S583478
Figure Lengend Snippet: Intercellular communication between POSTN + CAFs and APOE + TAMs in LSCC. ( A ) Global ligand–receptor interaction networks reveal strong bidirectional communication between POSTN + CAFs and APOE + TAMs. ( B ) Outgoing signaling patterns from POSTN + CAFs. ( C ) Outgoing signaling patterns from APOE + TAMs. (In figure A-C, the numbers on the edges indicate the amount of inferred significant intercellular interactions between cell populations.) ( D ) Bubble plots highlight significant ligand–receptor pairs mediating communication from POSTN + CAFs. ( E ) GO enrichment indicates chemotaxis and apoptotic signaling modulation as major biological processes (from POSTN + CAFs to APOE + TAMs). ( F ) KEGG analysis identifies cytokine-cytokine receptor interactions, complement/coagulation as dominant pathways (from POSTN + CAFs to APOE + TAMs). ( G ) Bubble plots highlight significant ligand–receptor pairs mediating communication from APOE + TAMs. ( H ) GO enrichment indicates chemotaxis and apoptotic signaling modulation as major biological processes (from APOE + TAMs to POSTN + CAFs). ( I ) KEGG analysis identifies proteoglycans in cancer, cytokine-cytokine receptor interaction as dominant pathways (from APOE + TAMs to POSTN + CAFs).
Article Snippet: Sections were then incubated with primary
Techniques: Chemotaxis Assay, Coagulation
Journal: International Journal of General Medicine
Article Title: A POSTN + CAF/APOE + TAM Axis is Associated with Tumor Progression and Potential Immunotherapy Resistance in Laryngeal Squamous Cell Carcinoma
doi: 10.2147/IJGM.S583478
Figure Lengend Snippet: Correlation and spatial colocalization between POSTN + CAFs and APOE + TAMs in LSCC. ( A – C ) Scatter plots showing the positive correlation between POSTN + CAF abundance and APOE + TAM abundance across multiple cohorts, including TCGA-HNSC, GSE41613 , and GSE65858 . Shaded areas represent 95% confidence intervals, and the correlation was evaluated using Spearman’s test. ( D ) Representative multiplex immunofluorescence staining images of LSCC tissues showing colocalization of POSTN (red) and APOE (green) proteins. DAPI (blue) marks cell nuclei.
Article Snippet: Sections were then incubated with primary
Techniques: Multiplex Assay, Immunofluorescence, Staining
Journal: International Journal of General Medicine
Article Title: A POSTN + CAF/APOE + TAM Axis is Associated with Tumor Progression and Potential Immunotherapy Resistance in Laryngeal Squamous Cell Carcinoma
doi: 10.2147/IJGM.S583478
Figure Lengend Snippet: Protein–protein interaction between POSTN and APOE. ( A ) Structural model of the POSTN-APOE complex; the inset highlights key hydrogen-bonding and hydrophobic interactions. ( B and C ) Electrostatic potential maps of POSTN ( B ) and APOE ( C ), showing charge complementarity at the interface. ( D ) A 2D interaction diagram illustrating hydrogen bonds and hydrophobic contacts between key residues. Symbols used: red lines for hydrogen bonds, blue circles for non-ligand bonds, and pink arcs for hydrophobic contacts.
Article Snippet: Sections were then incubated with primary
Techniques:
Journal: International Journal of General Medicine
Article Title: A POSTN + CAF/APOE + TAM Axis is Associated with Tumor Progression and Potential Immunotherapy Resistance in Laryngeal Squamous Cell Carcinoma
doi: 10.2147/IJGM.S583478
Figure Lengend Snippet: Prognostic and functional implications of POSTN + CAFs and APOE + TAMs co-enrichment. ( A ) Kaplan-Meier survival analysis shows the worst outcomes in the POSTN + CAFs high /APOE + TAMs high group. ( B ) GO analysis reveals enrichment in extracellular matrix organization and collagen regulation in the POSTN + CAFs high /APOE + TAMs high group. ( C ) GSEA indicates activation of EMT, antigen presentation, neuroactive ligand–receptor signaling, and TGF-β pathways in the POSTN + CAFs high /APOE + TAMs high group.
Article Snippet: Sections were then incubated with primary
Techniques: Functional Assay, Activation Assay, Immunopeptidomics
Journal: International Journal of General Medicine
Article Title: A POSTN + CAF/APOE + TAM Axis is Associated with Tumor Progression and Potential Immunotherapy Resistance in Laryngeal Squamous Cell Carcinoma
doi: 10.2147/IJGM.S583478
Figure Lengend Snippet: Association of the POSTN + CAFs/APOE + TAMs axis with immune suppression and ICI resistance. ( A ) TME immune cell infiltration across LSCC clinical subgroups quantified by five deconvolution algorithms. ( B ) High POSTN + CAFs/APOE + TAMs enrichment LSCC shows increased stromal and immune scores but reduced tumor purity, as well as TIDE scores with a tendency to be higher. ( C – E ) The IMvigor210 cohort validates poorer survival in POSTN + CAFs high /APOE + TAMs high patients. ( F ) Treatment-response comparison shows a higher proportion of PD/SD in the high-risk group ( χ² -test).
Article Snippet: Sections were then incubated with primary
Techniques: Comparison
Journal: The World Journal of Men's Health
Article Title: Comprehensive Analysis of N6-Methyladenosine Modification Profiling in Diabetic Erectile Dysfunction
doi: 10.5534/wjmh.240328
Figure Lengend Snippet: Subpopulation distribution of hub genes. (A) Clustering visualization of subpopulations in the corpus cavernosum. (B) Expression distribution of hub genes in different cells of corpus cavernosum. The expression distribution of POSTN (C, D) and LOX (E, F) in the tissue of corpus cavernosum. UMAP: uniform manifold approximation and projection, EC: endothelial cell, FB: fibroblast, SMC: smooth muscle cell, SWC: Schwann cell, MAC: macrophage, T: T cell.
Article Snippet: Similarly, the sections of corpus cavernosum were subjected to immunohistochemistry to detect the protein expression of
Techniques: Expressing
Journal: bioRxiv
Article Title: WISP1 drives a mechanically active immune modulatory and proliferative cardiac myofibroblast state
doi: 10.64898/2026.02.17.706476
Figure Lengend Snippet: (A) Periostin ( Postn ) expression assessed by qPCR in primary cardiac fibroblasts treated for 72 h. (B-C) Representative Western blot (B) and densitometry normalized to GAPDH and Ctrl (C) of Periostin across 6 biological replicates. (D-E) Representative Western blots for α-SMA (D) and densitometric quantification (E) following treatment with p38 MAPK inhibitor SB203580 (10 μM). (F-G) Representative Western blots for periosotin (F) and densitometric quantification (G) following treatment with p38 MAPK inhibitor SB203580 (10 μM). (H) Total soluble collagen secretion measured by Picrosirius Red. Data are mean ± SEM. Statistical significance was determined by one-way ANOVA or two-way ANOVA as appropriate.
Article Snippet: Membranes were incubated overnight at 4 °C with primary antibodies (1:1,000 in 5% BSA):
Techniques: Expressing, Western Blot