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PRKDC and SLC25A13‐oriented drug framework identification for ESCC patients. (A) GSCA enrichment analysis for identification of sensitive drugs targeting PRKDC and SLC25A13. (B,C) Sensitivity analysis of drugs for ESCC patients. (D) CCK‐8 assays for optimum concentration of Navitoclax <t>and</t> <t>BX‐912</t> in KYSE150 cell lines. (E) CCK‐8 assay for evaluation of Navitoclax and BX‐912 in KYSE150 cell line growth. (F) Wound‐healing assays following Navitoclax and BX‐912 treatment in KYSE150 cells. Data was presented as mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. Scale bar = 200 μm.
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PRKDC and SLC25A13‐oriented drug framework identification for ESCC patients. (A) GSCA enrichment analysis for identification of sensitive drugs targeting PRKDC and SLC25A13. (B,C) Sensitivity analysis of drugs for ESCC patients. (D) CCK‐8 assays for optimum concentration of <t>Navitoclax</t> and BX‐912 in KYSE150 cell lines. (E) CCK‐8 assay for evaluation of Navitoclax and BX‐912 in KYSE150 cell line growth. (F) Wound‐healing assays following Navitoclax and BX‐912 treatment in KYSE150 cells. Data was presented as mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. Scale bar = 200 μm.
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PRKDC and SLC25A13‐oriented drug framework identification for ESCC patients. (A) GSCA enrichment analysis for identification of sensitive drugs targeting PRKDC and SLC25A13. (B,C) Sensitivity analysis of drugs for ESCC patients. (D) CCK‐8 assays for optimum concentration of <t>Navitoclax</t> and BX‐912 in KYSE150 cell lines. (E) CCK‐8 assay for evaluation of Navitoclax and BX‐912 in KYSE150 cell line growth. (F) Wound‐healing assays following Navitoclax and BX‐912 treatment in KYSE150 cells. Data was presented as mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. Scale bar = 200 μm.
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PRKDC and SLC25A13‐oriented drug framework identification for ESCC patients. (A) GSCA enrichment analysis for identification of sensitive drugs targeting PRKDC and SLC25A13. (B,C) Sensitivity analysis of drugs for ESCC patients. (D) CCK‐8 assays for optimum concentration of <t>Navitoclax</t> and BX‐912 in KYSE150 cell lines. (E) CCK‐8 assay for evaluation of Navitoclax and BX‐912 in KYSE150 cell line growth. (F) Wound‐healing assays following Navitoclax and BX‐912 treatment in KYSE150 cells. Data was presented as mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. Scale bar = 200 μm.
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PRKDC and SLC25A13‐oriented drug framework identification for ESCC patients. (A) GSCA enrichment analysis for identification of sensitive drugs targeting PRKDC and SLC25A13. (B,C) Sensitivity analysis of drugs for ESCC patients. (D) CCK‐8 assays for optimum concentration of Navitoclax and BX‐912 in KYSE150 cell lines. (E) CCK‐8 assay for evaluation of Navitoclax and BX‐912 in KYSE150 cell line growth. (F) Wound‐healing assays following Navitoclax and BX‐912 treatment in KYSE150 cells. Data was presented as mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. Scale bar = 200 μm.

Journal: Cancer Medicine

Article Title: Identification and Validation of cGAS ‐ STING Pathway‐Associated Predictive and Therapeutic Models for Esophageal Squamous Cell Cancer Patients via Artificial Intelligence and Multi‐Omics

doi: 10.1002/cam4.71645

Figure Lengend Snippet: PRKDC and SLC25A13‐oriented drug framework identification for ESCC patients. (A) GSCA enrichment analysis for identification of sensitive drugs targeting PRKDC and SLC25A13. (B,C) Sensitivity analysis of drugs for ESCC patients. (D) CCK‐8 assays for optimum concentration of Navitoclax and BX‐912 in KYSE150 cell lines. (E) CCK‐8 assay for evaluation of Navitoclax and BX‐912 in KYSE150 cell line growth. (F) Wound‐healing assays following Navitoclax and BX‐912 treatment in KYSE150 cells. Data was presented as mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. Scale bar = 200 μm.

Article Snippet: BX‐912 (HY‐11005) and Navitoclax (HY‐10087) were purchased from MCE (China).

Techniques: CCK-8 Assay, Concentration Assay

PRKDC and SLC25A13‐oriented drug framework identification for ESCC patients. (A) GSCA enrichment analysis for identification of sensitive drugs targeting PRKDC and SLC25A13. (B,C) Sensitivity analysis of drugs for ESCC patients. (D) CCK‐8 assays for optimum concentration of Navitoclax and BX‐912 in KYSE150 cell lines. (E) CCK‐8 assay for evaluation of Navitoclax and BX‐912 in KYSE150 cell line growth. (F) Wound‐healing assays following Navitoclax and BX‐912 treatment in KYSE150 cells. Data was presented as mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. Scale bar = 200 μm.

Journal: Cancer Medicine

Article Title: Identification and Validation of cGAS ‐ STING Pathway‐Associated Predictive and Therapeutic Models for Esophageal Squamous Cell Cancer Patients via Artificial Intelligence and Multi‐Omics

doi: 10.1002/cam4.71645

Figure Lengend Snippet: PRKDC and SLC25A13‐oriented drug framework identification for ESCC patients. (A) GSCA enrichment analysis for identification of sensitive drugs targeting PRKDC and SLC25A13. (B,C) Sensitivity analysis of drugs for ESCC patients. (D) CCK‐8 assays for optimum concentration of Navitoclax and BX‐912 in KYSE150 cell lines. (E) CCK‐8 assay for evaluation of Navitoclax and BX‐912 in KYSE150 cell line growth. (F) Wound‐healing assays following Navitoclax and BX‐912 treatment in KYSE150 cells. Data was presented as mean ± SD, * p < 0.05, ** p < 0.01, *** p < 0.001. Scale bar = 200 μm.

Article Snippet: BX‐912 (HY‐11005) and Navitoclax (HY‐10087) were purchased from MCE (China).

Techniques: CCK-8 Assay, Concentration Assay