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GC protein is a key factor involved in the PNI of PDAC. A) Representative H&E images showed the nerves in PNI‐low and PNI‐high PDAC samples; the asterisk indicates nerves, arrow represent cancer cells, scale bar, 100 µm. B) Kyoto Encyclopedia of Genes and Genomes (KEGG) annotation of differentially expressed genes (DEGs) between PNI‐low and PNI‐high group. C) Venn diagram showed the filter criteria of the candidate DEGs between the PNI‐low and PNI‐high groups. D) Single cell RNA sequencing analysis showed the expression pattern of CRISP3, SCGB3A1, CGB5, <t>CXADR,</t> CST6, <t>DEFB1,</t> <t>TCN1,</t> PCSK2, SERPINA4, CFC1, GC, SERPINA5 , and SPINK1 in human PDAC tissues. Data were obtained from CRA001160 and GSE202051 . E) Representative immunohistochemical staining of CRISP3, TCN1, SCGB3A1, CXADR, and GC protein expression level in human PDAC tissues in the Ren Ji cohort, scale bar, 100 µm. F) The association between CRISP3, TCN1, SCGB3A1, CXADR, and GC expression level and PNI degree in PDAC tissue in the Ren Ji cohort (n = 134). The yellow, cyan, turquoise, and purple represented ‐, +, ++, and +++ expression level of indicated proteins, respectively. G) Representative immunohistochemical staining of GC protein in human PDAC tissues from the Ren Ji cohort. The asterisk indicates nerves, and arrow represents cancer cells; scale bar, 100 µm. H) Immunofluorescence analysis showed the expression pattern of GC protein in the PNI‐low and PNI‐high human PDAC tissues. Scale bar, 50 µm. **** P < 0.0001.
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GC protein is a key factor involved in the PNI of PDAC. A) Representative H&E images showed the nerves in PNI‐low and PNI‐high PDAC samples; the asterisk indicates nerves, arrow represent cancer cells, scale bar, 100 µm. B) Kyoto Encyclopedia of Genes and Genomes (KEGG) annotation of differentially expressed genes (DEGs) between PNI‐low and PNI‐high group. C) Venn diagram showed the filter criteria of the candidate DEGs between the PNI‐low and PNI‐high groups. D) Single cell RNA sequencing analysis showed the expression pattern of CRISP3, SCGB3A1, CGB5, CXADR, CST6, DEFB1, TCN1, PCSK2, SERPINA4, CFC1, GC, SERPINA5 , and SPINK1 in human PDAC tissues. Data were obtained from CRA001160 and GSE202051 . E) Representative immunohistochemical staining of CRISP3, TCN1, SCGB3A1, CXADR, and GC protein expression level in human PDAC tissues in the Ren Ji cohort, scale bar, 100 µm. F) The association between CRISP3, TCN1, SCGB3A1, CXADR, and GC expression level and PNI degree in PDAC tissue in the Ren Ji cohort (n = 134). The yellow, cyan, turquoise, and purple represented ‐, +, ++, and +++ expression level of indicated proteins, respectively. G) Representative immunohistochemical staining of GC protein in human PDAC tissues from the Ren Ji cohort. The asterisk indicates nerves, and arrow represents cancer cells; scale bar, 100 µm. H) Immunofluorescence analysis showed the expression pattern of GC protein in the PNI‐low and PNI‐high human PDAC tissues. Scale bar, 50 µm. **** P < 0.0001.

Journal: Advanced Science

Article Title: Vitamin D Binding Protein, a Ligand of Integrin beta 1, Motivates Both Tumor Cells and Schwann Cells to Promote Perineural Invasion in Pancreatic Ductal Adenocarcinoma

doi: 10.1002/advs.202511726

Figure Lengend Snippet: GC protein is a key factor involved in the PNI of PDAC. A) Representative H&E images showed the nerves in PNI‐low and PNI‐high PDAC samples; the asterisk indicates nerves, arrow represent cancer cells, scale bar, 100 µm. B) Kyoto Encyclopedia of Genes and Genomes (KEGG) annotation of differentially expressed genes (DEGs) between PNI‐low and PNI‐high group. C) Venn diagram showed the filter criteria of the candidate DEGs between the PNI‐low and PNI‐high groups. D) Single cell RNA sequencing analysis showed the expression pattern of CRISP3, SCGB3A1, CGB5, CXADR, CST6, DEFB1, TCN1, PCSK2, SERPINA4, CFC1, GC, SERPINA5 , and SPINK1 in human PDAC tissues. Data were obtained from CRA001160 and GSE202051 . E) Representative immunohistochemical staining of CRISP3, TCN1, SCGB3A1, CXADR, and GC protein expression level in human PDAC tissues in the Ren Ji cohort, scale bar, 100 µm. F) The association between CRISP3, TCN1, SCGB3A1, CXADR, and GC expression level and PNI degree in PDAC tissue in the Ren Ji cohort (n = 134). The yellow, cyan, turquoise, and purple represented ‐, +, ++, and +++ expression level of indicated proteins, respectively. G) Representative immunohistochemical staining of GC protein in human PDAC tissues from the Ren Ji cohort. The asterisk indicates nerves, and arrow represents cancer cells; scale bar, 100 µm. H) Immunofluorescence analysis showed the expression pattern of GC protein in the PNI‐low and PNI‐high human PDAC tissues. Scale bar, 50 µm. **** P < 0.0001.

Article Snippet: The primary antibodies were listed as follows: GC (1:100, Proteintech, 16922‐1‐AP, RRID: AB_10597098), ITGB1 (1:100, Proteintech, 12594‐1‐AP, RRID: AB_2130085), FAK (1:1000, Cell Signaling Technology, 71433, RRID: AB_2799801), p‐FAK (Tyr397) (1:50, Cell Signaling Technology, 8556, RRID: AB_10891442), PGP9.5 (1:4000, Proteintech, 66230‐1‐Ig, RRID: AB_2881621), CRISP3 (1:500, Proteintech, 14847‐1‐AP, RRID: AB_1607510), TCN1 (1:100, Proteintech, 16078‐1‐AP, RRID: AB_2878215), SCGB3A1 (1:100, Novus, NBP1‐36983, RRID: AB_2183538), CXADR (1:100, Proteintech, 11777‐1‐AP, RRID: AB_2087443), and HPR‐link secondary antibodies (anti‐Rb, 1:5000, ab205718, RRID: AB_2819160, anti‐Ms, 1:5000, ab205719, RRID: AB_2755049, Abcam, USA).

Techniques: RNA Sequencing, Expressing, Immunohistochemical staining, Staining, Immunofluorescence