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Potential agents for patients with high SRS. (A) Identification of significantly activated pathways in the SRS-high group using the GSEA algorithm. (B) Predicting oxaliplatin sensitivity to assess the computational algorithm’s feasibility. (C, D) Analyzing correlation and differences in drug sensitivity for potential candidates from the CTRP and PRISM datasets. (E–H) Conducting molecular docking studies between SEMA4C and the compounds tanespimycin, clofarabine, nutlin-3, and LGX818.

Journal: Frontiers in Immunology

Article Title: Integrative analysis of semaphorins family genes in colorectal cancer: implications for prognosis and immunotherapy

doi: 10.3389/fimmu.2025.1536545

Figure Lengend Snippet: Potential agents for patients with high SRS. (A) Identification of significantly activated pathways in the SRS-high group using the GSEA algorithm. (B) Predicting oxaliplatin sensitivity to assess the computational algorithm’s feasibility. (C, D) Analyzing correlation and differences in drug sensitivity for potential candidates from the CTRP and PRISM datasets. (E–H) Conducting molecular docking studies between SEMA4C and the compounds tanespimycin, clofarabine, nutlin-3, and LGX818.

Article Snippet: Membranes were blocked using 5% skim milk in TBST and incubated with primary antibodies against SEMA4C (1:3000, Cat. no: 28402-1-AP; Proteintech) and β-actin (1:1000, Cat. no: TA09; OriGene Technologies, Inc.).

Techniques:

Verification of the tumor-promoting effect of SEMA4C in CRC. (A) Western blot analysis of SEMA4C expression in HT29 and SW480 cell lines. (B, C) CCK-8 and colony formation assays were conducted to evaluate the impact of SEMA4C downregulation on the proliferation and viability of HT29 and SW480 cell lines. (D–F) Transwell assays were performed to evaluate the influence of SEMA4C downregulation on the cell migration and invasion. (G) Impact of SEMA4C downregulation on the cell apoptosis was analyzed by flow cytometry assay. (*: P < 0.05; **: P < 0.01; ***: P < 0.001).

Journal: Frontiers in Immunology

Article Title: Integrative analysis of semaphorins family genes in colorectal cancer: implications for prognosis and immunotherapy

doi: 10.3389/fimmu.2025.1536545

Figure Lengend Snippet: Verification of the tumor-promoting effect of SEMA4C in CRC. (A) Western blot analysis of SEMA4C expression in HT29 and SW480 cell lines. (B, C) CCK-8 and colony formation assays were conducted to evaluate the impact of SEMA4C downregulation on the proliferation and viability of HT29 and SW480 cell lines. (D–F) Transwell assays were performed to evaluate the influence of SEMA4C downregulation on the cell migration and invasion. (G) Impact of SEMA4C downregulation on the cell apoptosis was analyzed by flow cytometry assay. (*: P < 0.05; **: P < 0.01; ***: P < 0.001).

Article Snippet: Membranes were blocked using 5% skim milk in TBST and incubated with primary antibodies against SEMA4C (1:3000, Cat. no: 28402-1-AP; Proteintech) and β-actin (1:1000, Cat. no: TA09; OriGene Technologies, Inc.).

Techniques: Western Blot, Expressing, CCK-8 Assay, Migration, Flow Cytometry