Journal: bioRxiv

Article Title: Imaging-Guided Metabolic Radiosensitization of Pediatric Rhabdoid Tumors

doi: 10.1101/2024.08.09.607364

Figure Lengend Snippet: (A) Whole tissue imaging and ( B ) confocal micrographs of γ-H2AX immunofluorescence staining of all treatment groups on Day 9. (Insets) Stained A-204 tissue at high magnification. Scale bar = 50 µm for confocal images and scale bar = 1000 µm for whole tumor sections. (C) Quantification of γ-H2AX staining in whole tumor sections ( a ) and confocal micrographs ( b ) of all treatment groups. (D) H&E staining for heart, liver, kidney and muscle from various treatment groups. Scale bar=100 µm. Data represented as mean ± SD.

Article Snippet: Alexa Fluor 488 AffiniPure Donkey Anti-Rat lgG(H+L) (Lot 163136) and Rhodamine (TRITC) AffiniPure Donkey Anti-Rat lgG(H+L) (Lot 157518) were obtained from Jackson ImmunoResearch Inc. Histone H2AX antibody (NB100-384) was purchased from Novus Biologicals and secondary antibody Donkey anti-Rabbit lgG (H+L) Dylight594 (SA5-10040) from Invitrogen.

Techniques: Imaging, Immunofluorescence, Staining

Journal: European Journal of Nuclear Medicine and Molecular Imaging

Article Title: Combining [ 177 Lu]Lu-DOTA-TOC PRRT with PARP inhibitors to enhance treatment efficacy in small cell lung cancer

doi: 10.1007/s00259-024-06844-1

Figure Lengend Snippet: Determination of γH2AX foci formation and clonogenic survival in H446 cells. (A) Exemplary images of H446 cells after mono- or combination therapy directly after treatment or after a 23 h post-incubation time. (B) Number of γH2AX foci per cell after mono- or combination therapy directly after treatment or after a 23 h post-incubation time in medium. Displayed are mean ± SEM from 3 individual experiments. (C) Surviving fractions of H446 cells mono- or combination therapy. Displayed are mean values from 2 independent experiments

Article Snippet: 1:150 dilution), γH2AX (pSER139, Novus #NB100-2280, 1:500 dilution) with optimized protocols of the Comparative Experimental Pathology Core Facility.

Techniques: Incubation

Journal: European Journal of Nuclear Medicine and Molecular Imaging

Article Title: Combining [ 177 Lu]Lu-DOTA-TOC PRRT with PARP inhibitors to enhance treatment efficacy in small cell lung cancer

doi: 10.1007/s00259-024-06844-1

Figure Lengend Snippet: Immunohistochemistry of H69 tumors. Exemplary stainings of H69 tumors obtained from the single dose PRRT study ( n = 1 animal/group) for SSTR2, PARP1, γH2AX (DNA damage marker) and cleaved caspase 3 (apoptosis marker) are displayed. Scale bar = 100 µm. Brown color indicates positivity for the respective marker

Article Snippet: 1:150 dilution), γH2AX (pSER139, Novus #NB100-2280, 1:500 dilution) with optimized protocols of the Comparative Experimental Pathology Core Facility.

Techniques: Immunohistochemistry, Marker

Journal: The Journal of Cell Biology

Article Title: Stemness factor Sall4 is required for DNA damage response in embryonic stem cells

doi: 10.1083/jcb.201408106

Figure Lengend Snippet: Sall4 −/− ESCs are impaired in ATM activation and hypersensitive to DOX treatment. (A) Phosphorylation of ATM, H2AX, and p53 in Sall4 +/− and Sall4 −/− ESCs at different time points after DOX treatment. (B and C) Sall4 +/− and Sall4 −/− ESCs were mixed, treated with DOX or mock treated, and examined for the foci formation by ATM-Ser1987p (B) or γ-H2AX (C). DNA is counterstained with DAPI (blue). Bars, 10 µm. Graphs show the change of average fluorescence intensity (AFI) determined by dividing the overall mean fluorescence intensity by the area of the cell, and values are mean ± SEM. **, P < 0.01; ***, P < 0.001 by t test throughout the figure. (D) Cell cycle G 2 /M checkpoint is impaired in Sall4 −/− ESCs after DOX treatment. (top) Mock-treated control. (bottom) 1 h after after DOX treatment. The values are means ± SEM ( n = 4). *, P < 0.05 by t test. Circles denote the percentages of cells positive for histone 3 phosphorylated at Ser10 in all cells. PI-A, propidium iodide area. (E) Inducible expression of Sall4 in Sall4 −/− ESCs rescues the activation of ATM after DOX (0.5 µM) treatment. Sall4 −/− ESCs were stably transfected with a doxycycline-inducible vector expressing ectopic Sall4 (Lenti- Sall4 ).

Article Snippet: After permeabilization with 0.4% Triton X-100, the cells were blocked in 3% BSA and then labeled with rabbit or mouse antibodies against Sall4 ab29112 (Abcam) or sc-101147, respectively; pATM (Ser 1981; 200–301-400; ROCKLAND); γ-H2AX; Baf60a; and Rad50 overnight at 4°C.

Techniques: Activation Assay, Phospho-proteomics, Fluorescence, Control, Expressing, Stable Transfection, Transfection, Plasmid Preparation

Journal: The Journal of Cell Biology

Article Title: Stemness factor Sall4 is required for DNA damage response in embryonic stem cells

doi: 10.1083/jcb.201408106

Figure Lengend Snippet: Sall4 is relocated from the heterochromatin to DNA DSBs in ESCs after DOX treatment. (A) Sall4 is sequestered in the heterochromatin and relocated to DNA DSBs in ESCs after DNA damage. Sall4 +/− cells were examined for the foci formation of γ-H2AX and Sall4 before and after DNA DSB damage induced by DOX. Nuclei were counterstained with DAPI (blue). For intensity correlation analysis (ICA), pixels from the Sall4 channel covarying positively with the corresponding signal from the γ-H2AX or DAPI channel are denoted. Bar, 5 µm. (B) Rr analysis for the colocalization of Sall4 and γ-H2AX. Rr is the Pearson’s correlation coefficient, and a value of 1 indicates perfect colocalization. The values of Rr are means ± SEM. ***, P < 0.001 by t test. (C) Sall4 is colocalized with HP1-α foci before DNA DSB damage and is mobilized out of HP1-α foci after DNA damage. Nuclei are counterstained with DAPI (blue). Bar, 5 µm. (D) The average fluorescence intensity (AFI) of Sall4 at heterochromatin was determined by dividing the overall mean fluorescence intensity by the area of the cell, and values are means ± SEM. **, P < 0.01 by t test. (E) DNA damage disrupts the interaction between Sall4 and HP1-α in ESCs. The interaction between Sall4 and HP1-α was analyzed by coimmunoprecipitation (Co-IP) with the HP1-α antibody.

Article Snippet: After permeabilization with 0.4% Triton X-100, the cells were blocked in 3% BSA and then labeled with rabbit or mouse antibodies against Sall4 ab29112 (Abcam) or sc-101147, respectively; pATM (Ser 1981; 200–301-400; ROCKLAND); γ-H2AX; Baf60a; and Rad50 overnight at 4°C.

Techniques: Fluorescence, Co-Immunoprecipitation Assay

Journal: The Journal of Cell Biology

Article Title: Stemness factor Sall4 is required for DNA damage response in embryonic stem cells

doi: 10.1083/jcb.201408106

Figure Lengend Snippet: Sall4 linking SWI/SNF-associated chromatin remodeling to MRN-dependent ATM activation. (A) Silencing of Baf60a impairs the recruitment of Sall4 to γ-H2AX foci after DNA DSB damage. Nuclei are counterstained with DAPI (blue). For intensity correlation analysis (ICA), pixels from the Sall4 channel covarying positively with the corresponding signal from the γ-H2AX channel are denoted. si-Con, control siRNA. Bar, 5 µm. (B) Inhibition of H3K14ac by CPTH2 disrupts the association of Baf60a, Sall4, and ATM with DNA DSBs in the cellular extract of Sall4 +/− ESCs treated with 0.5 µM DOX for 4 h. WNE, whole nuclear extract. (C) Inhibition of H3K14ac by CPTH2 in Sall4 +/− ESCs impaired ATM-dependent responses to DNA DSB damage. (D) The kinetics of the recruitment of Rad50, Sall4, and Balf60a to the specific DNA DSB. ChIP analysis showed the kinetics of the recruitment of Sall4, Rad50, and Baf60a to the single I-PpoI cleavage site at chromosome 3 in Sall4 +/− cells. Time denotes the minutes after the addition of 4-hydroxytamoxifen. Values are means ± SEM. (E) An illustrated model for Sall4 to function as a transducer of chromatin remodeling to ATM signaling in ESCs after DNA damage. P, phosphorylation.

Article Snippet: After permeabilization with 0.4% Triton X-100, the cells were blocked in 3% BSA and then labeled with rabbit or mouse antibodies against Sall4 ab29112 (Abcam) or sc-101147, respectively; pATM (Ser 1981; 200–301-400; ROCKLAND); γ-H2AX; Baf60a; and Rad50 overnight at 4°C.

Techniques: Activation Assay, Control, Inhibition, Phospho-proteomics