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Soy Isoflavones Augment Radiation Effect by Inhibiting APE1/Ref-1 DNA Repair Activity in Non-small Cell Lung Cancer  Vinita Singh-Gupta, PhD, Michael.

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Presentation on theme: "Soy Isoflavones Augment Radiation Effect by Inhibiting APE1/Ref-1 DNA Repair Activity in Non-small Cell Lung Cancer  Vinita Singh-Gupta, PhD, Michael."— Presentation transcript:

1 Soy Isoflavones Augment Radiation Effect by Inhibiting APE1/Ref-1 DNA Repair Activity in Non-small Cell Lung Cancer  Vinita Singh-Gupta, PhD, Michael C. Joiner, PhD, Lindsay Runyan, BSc, Christopher K. Yunker, BSc, Fazlul H. Sarkar, PhD, Steven Miller, MD, Shirish M. Gadgeel, MD, Andre A. Konski, MD, Gilda G. Hillman, PhD  Journal of Thoracic Oncology  Volume 6, Issue 4, Pages (April 2011) DOI: /JTO.0b013e ae Copyright © 2011 International Association for the Study of Lung Cancer Terms and Conditions

2 FIGURE 1 A549 cell growth inhibition by soy isoflavones and radiation. A, Soy dose titration. Cells were treated for 4 days with soy at concentration of 0, 10, 25, 50, 75, and 100 μM, and viable cells were counted. B, Radiation dose titration. Cells were irradiated with doses of 1, 2, 3, 5, 6, and 8 Gy, and viable cells were counted. Bars represent the mean number of cells of duplicate wells calculated as the percentage of control cells ± SE. *p < relative to control group. Journal of Thoracic Oncology 2011 6, DOI: ( /JTO.0b013e ae) Copyright © 2011 International Association for the Study of Lung Cancer Terms and Conditions

3 FIGURE 2 Survival fraction of A549 cells treated with soy and/or radiation. A, Survival of cells treated with soy. A549 cells were treated for 72 hours with soy at concentrations of 5, 7.5, 10, 15, 20, 25, and 30 μM and plated in a clonogenic assay. B, Survival of cells treated with radiation. A549 cells were irradiated with different doses of 1 to 10 Gy and plated in a clonogenic assay. Inset: the radiation dose survival curve is fitted by a nonlinear least-square regression according to the linear-quadratic formula (SAS JMPV7). C, Survival of cells treated with soy and radiation. A549 cells were pretreated with soy at 5, 7.5, and 10 μM for 72 hours, then irradiated at 3 Gy and plated in a clonogenic assay in the presence of the same concentration of soy. Inset in (C) shows the products of SF(S) and SF(R), which are the survival fraction of soy treatment at 5, 7.5, and 10 μM multiplied by the survival fraction of 3 Gy radiation SF(R). These products are greater than the survival fraction of cells treated with combined soy and radiation [SF(S + R)] at each concentration of soy tested. In panels A, B, and C, bars represent the mean survival fraction of triplicate wells ± SE. *p < represent significance of each treatment group relative to control group. Journal of Thoracic Oncology 2011 6, DOI: ( /JTO.0b013e ae) Copyright © 2011 International Association for the Study of Lung Cancer Terms and Conditions

4 FIGURE 3 Increased DNA double-strand breaks in A549 cells treated with soy and radiation. A549 cells were treated with soy at 30 μM for 24 hours then irradiated with 3 Gy and tested at 1 hour and 24 hours after radiation, corresponding to 24 and 48 hours of soy treatment, respectively. Control cells (con), cells treated with soy (soy), cells treated with radiation (Rad), and both combined (Soy + Rad) were processed for immunostaining of γ-H2AX to detect DNA double-strand breaks (DSBs). A, γ-H2AX staining at 1 hour after radiation or 24 hours after soy treatment. B, γ-H2AX staining at 24 hours after radiation or 48 hours after soy treatment. Journal of Thoracic Oncology 2011 6, DOI: ( /JTO.0b013e ae) Copyright © 2011 International Association for the Study of Lung Cancer Terms and Conditions

5 FIGURE 4 Effect of soy and radiation on HIF-1α and γ-H2AX in A549 cells. Cells were either untreated (Con for control) or pretreated with 30 μM soy, 3 Gy radiation (Rad), or combined (Soy + Rad). Cells were pretreated with soy for 24 hours, and then cells were irradiated. At 1 hour or 24 hours post radiation, corresponding to 24 and 48 hours soy treatment, cells were processed for Western blot analysis to detect γ-H2AX and HIF-1α. β-Actin protein levels served as a loading control. Journal of Thoracic Oncology 2011 6, DOI: ( /JTO.0b013e ae) Copyright © 2011 International Association for the Study of Lung Cancer Terms and Conditions

6 FIGURE 5 Pretreatment with soy inhibits APE-1/Ref-1 expression and HIF-1α and NF-κB DNA-binding activity induced by radiation. A549 cells were pretreated with 30 μM soy for 72 hours then irradiated at 3 Gy. At 5 hours after radiation, nuclear extracts were subjected to Western blot analysis or electrophoretic mobility shift assay (EMSA). Untreated control (Con), soy alone (Soy), radiation 3 Gy (Rad), and soy combined with radiation (Soy + Rad). A, Nuclear expression of APE1/Ref-1. Nuclear extracts (10 μg) were run on 10% Western gel and blotted against APE-1/Ref-1 Ab. B, HIF-1α DNA-binding activity. Nuclear extracts were incubated with IRDye-700-labeled HIF-1α oligonucleotide and subjected to EMSA. C, NF-κB DNA-binding activity. Nuclear extracts were incubated with IRDye-700-labeled NF-κB oligonucleotide and subjected to EMSA. In panels A, B, and C, data are also presented as the mean integrated density value (I.D.V.) of the band/μg protein loaded (±SE). *p < 0.05 and ** p <0.001 represent significance of each treatment group relative to control group. Dotted lines and p values in I.D.V. diagrams show the difference between cells treated with radiation + soy versus radiation only. Western blot for retinoblastoma (Rb) protein in the nuclear extract was performed as an internal loading control. Journal of Thoracic Oncology 2011 6, DOI: ( /JTO.0b013e ae) Copyright © 2011 International Association for the Study of Lung Cancer Terms and Conditions

7 FIGURE 6 Effect of APE1/Ref-1 inhibitors on γ-H2AX expression in A549 cells. A549 cells were pretreated with E3330 (50 μM), methoxyamine (20 mM), or soy isoflavones (30 μM) for 24 hours and then irradiated at 3 Gy. Cells were further incubated for 1 hour and 24 hours after radiation and then processed for γ-H2AX immunostaining. Control cells (Control), cells treated with radiation (Rad) and both combined (Soy + Rad), and cells treated with E3330 and radiation (E Rad) or methoxyamine and radiation (Methox + Rad) were processed for immunostaining of γ-H2AX to detect DNA double-strand breaks (DSBs). A, Mean number of γ-H2AX foci per cell. B, Mean percent of γ-H2AX-positive cells per field. In both (A) and (B) panels, bars represent the mean values ± SD calculated from three different fields. Journal of Thoracic Oncology 2011 6, DOI: ( /JTO.0b013e ae) Copyright © 2011 International Association for the Study of Lung Cancer Terms and Conditions

8 FIGURE 7 Effect of APE1/Ref-1 inhibitors on A549 cell growth. A549 cells were pretreated either with E3330 (25 μM) or methoxyamine (10 mM), or soy isoflavones (15 μM) or in combination (E soy or Methox + soy) for 24 hours and then irradiated with 3 Gy. Cells were further incubated, and viable cells were counted at 3 days after radiation. Single treatment and combined treatments of E3330, methoxyamine, and soy isoflavones are also shown. Bars represent the mean number of cells of duplicate wells calculated as the percentage of control cells ± SE. Dotted lines and p values show the difference between cells treated with single and combined treatments; *p < 0.05 and **p < Journal of Thoracic Oncology 2011 6, DOI: ( /JTO.0b013e ae) Copyright © 2011 International Association for the Study of Lung Cancer Terms and Conditions

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