Triple Negative Breast Neoplasms
|
0.040 |
Biomarker
|
disease |
BEFREE |
We hypothesized that the ATR inhibitor, VX-970 (now known as M6620), would preferentially radiosensitize TNBC.
|
30166399 |
2018 |
Triple-Negative Breast Carcinoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
We hypothesized that the ATR inhibitor, VX-970 (now known as M6620), would preferentially radiosensitize TNBC.
|
30166399 |
2018 |
Seckel syndrome
|
0.800 |
Biomarker
|
disease |
BEFREE |
We highlight a previous study from our laboratory demonstrating that UV-exposed, ATR-deficient Seckel syndrome fibroblasts, like XPV fibroblasts, manifest strong attenuation of GG-NER uniquely in S phase populations.
|
20457011 |
2010 |
Malignant Neoplasms
|
0.400 |
Biomarker
|
group |
BEFREE |
We here focus on the proteins ATM, ATR, CHK1 and WEE1, reviewing their roles in the DNA damage response and as targets in cancer therapy.
|
28961555 |
2017 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
We here focus on the proteins ATM, ATR, CHK1 and WEE1, reviewing their roles in the DNA damage response and as targets in cancer therapy.
|
28961555 |
2017 |
Lymphoma
|
0.020 |
Biomarker
|
group |
BEFREE |
We have reported micro-SPECT/CT imaging of Mec-1 human lymphoma xenografts in SCID mice, using [(111)In]DOTA-anti-bcl-2-PNA-Tyr(3)-octreotate.
|
26239085 |
2015 |
Adult Lymphoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
We have reported micro-SPECT/CT imaging of Mec-1 human lymphoma xenografts in SCID mice, using [(111)In]DOTA-anti-bcl-2-PNA-Tyr(3)-octreotate.
|
26239085 |
2015 |
Childhood Lymphoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
We have reported micro-SPECT/CT imaging of Mec-1 human lymphoma xenografts in SCID mice, using [(111)In]DOTA-anti-bcl-2-PNA-Tyr(3)-octreotate.
|
26239085 |
2015 |
Glioma
|
0.310 |
AlteredExpression
|
disease |
BEFREE |
We found that the expression of ATR, ChK1 and Chk2 in gliomas was significantly down-regulated relative to the normal brain tissues.
|
19969004 |
2010 |
Triple Negative Breast Neoplasms
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
We found that stress hormones induced DNA damage, phosphorylation of ATR, which was accompanied by an up-regulation of the G1 cell kinase inhibitor p21 and a cell cycle halt of TNBCs in the G1 phase. p21 knockdown abrogated G1 arrest by stress hormones.
|
25880007 |
2015 |
Triple-Negative Breast Carcinoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
We found that stress hormones induced DNA damage, phosphorylation of ATR, which was accompanied by an up-regulation of the G1 cell kinase inhibitor p21 and a cell cycle halt of TNBCs in the G1 phase. p21 knockdown abrogated G1 arrest by stress hormones.
|
25880007 |
2015 |
Ataxia Telangiectasia
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
We found that EBV triggered activation of the ataxia telangiectasia and Rad3-related (ATR) signaling pathway in the early rapidly proliferating cells, which were also significantly more sensitive to inhibition of the ATR pathway than late attenuated proliferating cells.
|
28604764 |
2017 |
Chondrosarcoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found that chondrosarcoma cells expressed very low basal levels of phosphorylated ATR, but cisplatin treatment induced the activation of ATR-Chk1 signaling in a dose- and time-dependent manner, suggesting the induction of DDR.
|
31839711 |
2019 |
Regular astigmatism - corneal
|
0.020 |
Biomarker
|
disease |
BEFREE |
We found a shift tendency of WTR to ATR with aging in anterior corneal astigmatism, while PCA remains ATR.
|
30104578 |
2018 |
Hypertensive disease
|
0.020 |
Biomarker
|
group |
BEFREE |
We concluded that ATR-AP205-001 vaccine quickly induced potent humoral immunity through collaboration of B cells, follicular dendritic cells and follicular helper T cells, providing an effective and safe intervention for hypertension in the future clinical application.
|
28974760 |
2017 |
Malignant Neoplasms
|
0.400 |
Biomarker
|
group |
BEFREE |
We conclude that an improved understanding of both similarities and differences in the cellular mechanisms among the cancer, normal and mESCs is crucial to develop a potential clinical relevance, and ATR-FITR can be successfully used as a novel approach to gain new insights into the stem cell and cancer research.
|
29497718 |
2018 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
We conclude that an improved understanding of both similarities and differences in the cellular mechanisms among the cancer, normal and mESCs is crucial to develop a potential clinical relevance, and ATR-FITR can be successfully used as a novel approach to gain new insights into the stem cell and cancer research.
|
29497718 |
2018 |
Nasopharyngeal carcinoma
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
We compared the expression levels of ATR kinases in human nasopharyngeal carcinoma, choriocarcinoma and chondrosarcoma cell lines.
|
31839711 |
2019 |
Kidney Failure, Chronic
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We analyzed the effects of the AGT M235T and ATR A1166C polymorphisms on hypertension and age at the end stage renal disease (ESRD).
|
12950120 |
2003 |
Chronic kidney disease stage 5
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We analyzed the effects of the AGT M235T and ATR A1166C polymorphisms on hypertension and age at the end stage renal disease (ESRD).
|
12950120 |
2003 |
Hypertensive disease
|
0.020 |
GeneticVariation
|
group |
BEFREE |
We analyzed the effects of the AGT M235T and ATR A1166C polymorphisms on hypertension and age at the end stage renal disease (ESRD).
|
12950120 |
2003 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We also show that LATS1 forms part of an ATR-mediated response to replication stress that requires the tumour suppressor RASSF1A.
|
25218637 |
2014 |
Nasopharyngeal carcinoma
|
0.030 |
Biomarker
|
disease |
BEFREE |
VTN, a previously identified BPIFB1-binding protein, was shown to induce cell proliferation and survival, G2/M phase arrest, DNA repair, activation of the ATM-Chk2 and ATR-Chk1 pathways, and anti-apoptotic effects after exposure to radiation, facilitating NPC cell radioresistance.
|
29568064 |
2018 |
Malignant neoplasm of breast
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Using western blotting it was shown that GA inhibited the protein expressions of MDC1, O(6)-methylguanine-DNA methyltransferase (MGMT), p-H2A.X, p53, DNA-dependent serine/threonine protein kinase (DNA-PK) and 14-3-3 proteins sigma (14-3-3σ) but increased p-p53, phosphate-ataxia-telangiectasia (p-H2A.X) and ataxia telangiectasia mutated and Rad3-related (p-ATR), phosphate-ataxia telangiectasia mutated (p-ATM) and breast cancer susceptibility protein 1 (BRCA1) in a 24-h treatment.
|
25862863 |
2015 |
Breast Carcinoma
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Using western blotting it was shown that GA inhibited the protein expressions of MDC1, O(6)-methylguanine-DNA methyltransferase (MGMT), p-H2A.X, p53, DNA-dependent serine/threonine protein kinase (DNA-PK) and 14-3-3 proteins sigma (14-3-3σ) but increased p-p53, phosphate-ataxia-telangiectasia (p-H2A.X) and ataxia telangiectasia mutated and Rad3-related (p-ATR), phosphate-ataxia telangiectasia mutated (p-ATM) and breast cancer susceptibility protein 1 (BRCA1) in a 24-h treatment.
|
25862863 |
2015 |