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HPV + UD-SCC-2 xenograft tissues exhibit a higher basal count of apoptotic and a lower number of senescent cells as compared with HPV − UM-SCC-74A tissues. A and B, Tumor growth control ( A ) and <t>Ki67</t> (proliferation), yH2AX (DNA damage), TUNEL (DNA fragmentation), and β-Gal (senescence) staining [ B ; representative pictures (top) and quantification (bottom)] of UM-SCC-74A xenografts after the indicated treatments (histologic cohort, n = 3–4). C and D, Tumor growth control ( C ) and Ki67, yH2AX, TUNEL, and β-Gal staining [ D ; representative pictures (top) and quantification (bottom)] of UD-SCC-2 xenografts after the indicated treatments (histologic cohort, n = 3–4). Data are analyzed with one-way ANOVA with post hoc multiple comparisons and are represented as the mean ± SEM; *, P < 0.05; **, P < 0.01; and ****, P < 0.0001.
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HPV + UD-SCC-2 xenograft tissues exhibit a higher basal count of apoptotic and a lower number of senescent cells as compared with HPV − UM-SCC-74A tissues. A and B, Tumor growth control ( A ) and <t>Ki67</t> (proliferation), yH2AX (DNA damage), TUNEL (DNA fragmentation), and β-Gal (senescence) staining [ B ; representative pictures (top) and quantification (bottom)] of UM-SCC-74A xenografts after the indicated treatments (histologic cohort, n = 3–4). C and D, Tumor growth control ( C ) and Ki67, yH2AX, TUNEL, and β-Gal staining [ D ; representative pictures (top) and quantification (bottom)] of UD-SCC-2 xenografts after the indicated treatments (histologic cohort, n = 3–4). Data are analyzed with one-way ANOVA with post hoc multiple comparisons and are represented as the mean ± SEM; *, P < 0.05; **, P < 0.01; and ****, P < 0.0001.
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HPV + UD-SCC-2 xenograft tissues exhibit a higher basal count of apoptotic and a lower number of senescent cells as compared with HPV − UM-SCC-74A tissues. A and B, Tumor growth control ( A ) and Ki67 (proliferation), yH2AX (DNA damage), TUNEL (DNA fragmentation), and β-Gal (senescence) staining [ B ; representative pictures (top) and quantification (bottom)] of UM-SCC-74A xenografts after the indicated treatments (histologic cohort, n = 3–4). C and D, Tumor growth control ( C ) and Ki67, yH2AX, TUNEL, and β-Gal staining [ D ; representative pictures (top) and quantification (bottom)] of UD-SCC-2 xenografts after the indicated treatments (histologic cohort, n = 3–4). Data are analyzed with one-way ANOVA with post hoc multiple comparisons and are represented as the mean ± SEM; *, P < 0.05; **, P < 0.01; and ****, P < 0.0001.

Journal: Molecular Cancer Therapeutics

Article Title: HPV and p53 Status as Precision Determinants of Head and Neck Cancer Response to DNA-PKcs Inhibition in Combination with Irradiation

doi: 10.1158/1535-7163.MCT-23-0794

Figure Lengend Snippet: HPV + UD-SCC-2 xenograft tissues exhibit a higher basal count of apoptotic and a lower number of senescent cells as compared with HPV − UM-SCC-74A tissues. A and B, Tumor growth control ( A ) and Ki67 (proliferation), yH2AX (DNA damage), TUNEL (DNA fragmentation), and β-Gal (senescence) staining [ B ; representative pictures (top) and quantification (bottom)] of UM-SCC-74A xenografts after the indicated treatments (histologic cohort, n = 3–4). C and D, Tumor growth control ( C ) and Ki67, yH2AX, TUNEL, and β-Gal staining [ D ; representative pictures (top) and quantification (bottom)] of UD-SCC-2 xenografts after the indicated treatments (histologic cohort, n = 3–4). Data are analyzed with one-way ANOVA with post hoc multiple comparisons and are represented as the mean ± SEM; *, P < 0.05; **, P < 0.01; and ****, P < 0.0001.

Article Snippet: The slices were incubated overnight at +4°C with a primary antibody targeting Ki67 (Cell Signaling Technology Cat. # 9027, RRID: AB_2636984) for both longitudinal and histologic cohorts and yH2AX (Cell Signaling Technology Cat. # 2577, RRID: AB_2118010) for the histologic cohort only.

Techniques: Control, TUNEL Assay, Staining