Binding of 53BP1 on uncapped telomeres.

Slides:



Advertisements
Similar presentations
Volume 14, Issue 4, Pages (May 2004)
Advertisements

AF647-RIS is internalized by TAMs in vivo.
DNA damage foci in irradiated cells.
A stochastic feedback loop model predicts the kinetics of DDR and growth arrest at the single cell level. A stochastic feedback loop model predicts the.
Fig. 6. AZD6738 induces DNA damage and apoptosis and exhibits antitumor efficacy in xenograft models of high-risk medulloblastoma and neuroblastoma. AZD6738.
DNA-damage (γ-H2AX) and telomere damage–induced foci (TIFs).
Telomere-Driven Tetraploidization Occurs in Human Cells Undergoing Crisis and Promotes Transformation of Mouse Cells  Teresa Davoli, Titia de Lange  Cancer.
Bay induced aggregation of Cp occurs in HBV-infected HepG2-NTCP cells.
Combined A2A receptor and PD-1 blockade is not effective in IFNγ−/− mice. Combined A2A receptor and PD-1 blockade is not effective in IFNγ−/− mice. AT-3ovadim.
BV6 increases tumor burden in bone.
Bortezomib sensitivity correlates with basal NF-κB activity in KP lung adenocarcinoma cell lines. Bortezomib sensitivity correlates with basal NF-κB activity.
Fig. 4. Antitumor efficacy of ERY974 against various cancer types.
XL184 effects on RIP-Tag2 tumor invasion and epithelial/mesenchymal markers. XL184 effects on RIP-Tag2 tumor invasion and epithelial/mesenchymal markers.
Antitumor effect of local cancer immunotherapy treatment toward distant B16F10 tumors. Antitumor effect of local cancer immunotherapy treatment toward.
Cytotoxic therapy induces CSF1-dependent macrophage recruitment.
BETi potentiate the efficacy of MEKi in NRAS‐mutant melanoma
Effects of in vivo Nutlin‐3 treatment on CSC content of Numb− and Numb+ tumors Effects of in vivo Nutlin‐3 treatment on CSC content of Numb− and Numb+
Imipramine and promethazine induce the apoptotic cell death of SCLC cells through activation of caspase-3. Imipramine and promethazine induce the apoptotic.
Telomere-Driven Tetraploidization Occurs in Human Cells Undergoing Crisis and Promotes Transformation of Mouse Cells  Teresa Davoli, Titia de Lange  Cancer.
DNA Damage Foci at Dysfunctional Telomeres
Fig. 2. BET inhibition enhances PARPi-induced DNA damage.
TDP1 knockdown increases the sensitivity of rhabdomyosarcoma cell lines to CPT treatment. TDP1 knockdown increases the sensitivity of rhabdomyosarcoma.
FAM134B-2 colocalizes with SERCA2 and SEC62.
Therapy-induced senescence of primary cells.
Mouse lymphoma model. Mouse lymphoma model. A, EL-Arf−/− cells (1 × 106) were tail-vein injected into C57BL/6 mice. LNIWC imaging was separated into 2.
Gene expression changes associated with response to combination CPI-444 and anti–PD-L1 treatment in MC38 tumors. Gene expression changes associated with.
Effect of mitomycin C and bortezomib on the growth of LS174T intraperitoneal tumors. Effect of mitomycin C and bortezomib on the growth of LS174T intraperitoneal.
GR cells are dependent upon sustained CDC25C signaling as pharmacologic or genetic inhibition of CDC25C induce synthetic lethality. GR cells are dependent.
coTCRcys-transduced T cells control tumor growth in vivo.
DNA recombination at sites of replication damage in BLM-deficient cells. DNA recombination at sites of replication damage in BLM-deficient cells. A. Nucleotide.
TSA-mediated changes in cell cycle inhibitor proteins.
Distribution of γ-H2AX foci on metaphase spreads from BLM-proficient and BLM-deficient cells. Distribution of γ-H2AX foci on metaphase spreads from BLM-proficient.
Selective delivery of pIC/PPHAffibody decreases the survival of HER2-overexpressing cells. Selective delivery of pIC/PPHAffibody decreases the survival.
DNA damage-induced RPA foci in asynchronous cells labeled with BUdR.
Targeting HR via CDK inhibition resensitizes recurrent cultures to temozolomide (TMZ). Targeting HR via CDK inhibition resensitizes recurrent cultures.
ERK reactivation following EGFR TKI treatment.
Rif/mDia2 signaling in primary tumor formation and spontaneous metastasis. Rif/mDia2 signaling in primary tumor formation and spontaneous metastasis. A,
Combination of miR-520d-3p and EphA2 siRNA treatment shows enhanced EphA2 inhibition and antitumor efficiency in vitro. Combination of miR-520d-3p and.
Combination CDN and PD-L1 mAb treatment of established MOC1 tumors produces consistent tumor rejection. Combination CDN and PD-L1 mAb treatment of established.
Induction of DNA strand breaks by artesunate.
Neutralization of CSF1 and Ad5-HRG treatment.
SSTC-104 and LRP6 depletion effects on β-catenin and synovial sarcoma cells. SSTC-104 and LRP6 depletion effects on β-catenin and synovial sarcoma cells.
Apoptotic cell index percentage (a and b) and mitotic cell index percentage (c and d) in small intestinal (a and c) and midcolonic (b and d) crypts of.
A and B, intratumoral DC-AdCCL21 leads to reduction in growth rates of bilateral tumors. A and B, intratumoral DC-AdCCL21 leads to reduction in growth.
A to C, MetMAb shows strong antitumor activity in the KP4 orthotopic model of pancreatic cancer by ultrasound. A to C, MetMAb shows strong antitumor activity.
The efficacy of telomerase inhibition–based therapies, such as imetelstat, depends on the tumor telomere length at the beginning of treatment. The efficacy.
RUNX3 depletion induces cellular senescence in an ATM/ATR dependent, but p53-independent manner. RUNX3 depletion induces cellular senescence in an ATM/ATR.
Intraperitoneal or intratumoral injection of 6-thio-dG or 6-thioguanine. Intraperitoneal or intratumoral injection of 6-thio-dG or 6-thioguanine. A, 2.
Impact of eNOS expression and treatment with GSNO on prostate tumor growth. Impact of eNOS expression and treatment with GSNO on prostate tumor growth.
Pdcd4 expression inhibits AP-1 transactivation.
Comparison of in vivo activity of 4D5scFvZZ and 4D5scFv.
Tumor protection induced by therapeutic PLG vaccination in combination with blockade antibodies. Tumor protection induced by therapeutic PLG vaccination.
Mean percentage change from baseline in total IGF-I and the R1507 serum concentration values following a single i.v. administration of R mg/kg (n.
Wild-type mice weight following 6-thio-dG and 6-thioguanine treatment.
SW620 xenografts treated with combination siKRAS+siPIK3CA/B.
Efficacy of KM100 and/or MTX in BALB/c mice bearing subcutaneous TUBO tumors. Efficacy of KM100 and/or MTX in BALB/c mice bearing subcutaneous TUBO tumors.
Proliferation of TA3-Ha and TA3-St cells in vitro and in vivo.
PDL192 and inhibit the growth of xenograft tumors.
BEZ235 induces accelerated senescence after radiation (IR) in vitro.
Treatment with a Ron inhibitor significantly reduces metastatic outgrowth. Treatment with a Ron inhibitor significantly reduces metastatic outgrowth. A,
Heterogeneous resistance mechanisms develop in response to W+T combination treatment in the EGFRL858R/T790M genetically engineered mice. Heterogeneous.
GCS-100 selectively kills KRAS-addicted lung tumors.
Transgenic mice with constitutively active NIK show increased tumor growth in bone. Transgenic mice with constitutively active NIK show increased tumor.
BV6 increases bone metastasis.
Colonization with B. fragilis protects mice against development of colon cancer. Colonization with B. fragilis protects mice against development of colon.
Detection of microcalcifications in 4T1 mammary tumors and human breast tumor tissue. Detection of microcalcifications in 4T1 mammary tumors and human.
Depletion of CD8+, CD4+, and Ly6G+ cells in subcutaneous TUBO tumor-bearing BALB/c mice treated with KM100 + MTX. Depletions were conducted by intraperitoneal.
Greater influx of PMNs and ST using PEGPH20/shIDO-ST.
Wnt5A and ROR2 contribute to intrinsic resistance to BRAF inhibitors.
Parthenolide inhibits tumor promotion and increases p21 expression in vivo. Parthenolide inhibits tumor promotion and increases p21 expression in vivo.
Presentation transcript:

Binding of 53BP1 on uncapped telomeres. Binding of 53BP1 on uncapped telomeres. A, 6-thio-dG induced telomeric localization of 53BP1 in A549-derived tumor cells (representative data). Images were obtained by DeltaVision and then deconvoluted by Autoquant X3. Red dots show DNA damage (53BP1), green dots show telomeres, and yellow dots show TIF (DNA damage on telomeres) in merged images. Scale bars, 3 μm. B, TIF index (percentage of TIF-positive cells) of A549-derived tumor cells treated with 6-thio-dG. Cells with ≥4 or ≥5 53BP1 foci colocalizing with telomere were scored as TIF positive by Imaris software (n > 150 for control, n > 200 for 6-thio-dG treatment). SDs from two independent experiments. **, P = 0.0051; *, P < 0.05 (compared with control), in the unpaired Student t test. C, DNA-damage foci per cell. A549-derived tumor cells treated with 6-thio-dG (n > 150 for control, n > 200 for 6-thio-dG treatment; SDs from two independent experiments). ns, not significant differences in the unpaired Student t test (control vs. 6-thio-dG; control; DMSO treated). D, the tumor volume (mm3) of A549-derived tumor with 6-thio-dG administration. 2 mg/kg of 6-thio-dG or DMSO/PBS was injected to the A549-derived tumor for 17 days every 2 days, intraperitoneally. Ilgen Mender et al. Cancer Discovery 2015;5:82-95 ©2015 by American Association for Cancer Research