| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Sahika Cingir Koker, Ermira Jahja, Huma Shehwana, Ayse Gokce Keskus, Ozlen Kon. Cholinergic Receptor Nicotinic Alpha 5 (CHRNA5) RNAi is associated with cell cycle inhibition, apoptosis, DNA damage response and drug sensitivity in breast cancer. PloS one. vol 13. issue 12. 2019-05-10. PMID:30543688. |
our study suggests chrna5 rnai is associated with cell cycle inhibition, apoptosis as well as reduced ddr and increased drug sensitivity in breast cancer yet future studies are warranted since dose- and cell line-specific differences exist in response to chrna5 depletion. |
2019-05-10 |
2023-08-13 |
Not clear |
| Hailong Tang, Mimi Shu, Bo Dai, Li Xu, Baoxia Dong, Guangxun Gao, Xiequn Che. DNA damage response-initiated cytokine secretion in bone marrow stromal cells promotes chemoresistance of myeloma cells. Leukemia & lymphoma. vol 59. issue 9. 2019-03-18. PMID:29249192. |
these data indicate that dna-damaging drug triggers an atm-dependent ddr in bmscs, leading to increased cytokine secretion and resistance of myeloma cells to chemotherapy-induced apoptosis. |
2019-03-18 |
2023-08-13 |
Not clear |
| J Luis Espinoza, Mika Minam. Sensing Bacterial-Induced DNA Damaging Effects Frontiers in immunology. vol 9. 2019-02-28. PMID:29422899. |
in addition to well-defined outcomes, such as cell cycle arrest, apoptosis, and senescence, another consequence of ddr activation is the induction of natural killer group 2 member d ligands (nkg2d-ls) on the surface of stressed cells. |
2019-02-28 |
2023-08-13 |
human |
| Hui-Ling Ou, Björn Schumache. DNA damage responses and p53 in the aging process. Blood. vol 131. issue 5. 2019-02-01. PMID:29141944. |
conversely, radiation therapy and chemotherapy induce dna damage to drive cells into apoptosis or senescence as outcomes of the dna damage response (ddr). |
2019-02-01 |
2023-08-13 |
Not clear |
| Martina Magni, Giacomo Buscemi, Laura Zannin. Cell cycle and apoptosis regulator 2 at the interface between DNA damage response and cell physiology. Mutation research. Reviews in mutation research. vol 776. 2018-11-26. PMID:29807573. |
cell cycle and apoptosis regulator 2 (ccar2 or dbc1) is a human protein recently emerged as a novel and important player of the dna damage response (ddr). |
2018-11-26 |
2023-08-13 |
human |
| Shohei Miyata, Li-Yan Wang, Susumu Kitanak. 3EZ, 20Ac-ingenol induces cell-specific apoptosis in cyclin D1 over-expression through the activation of ATR and downregulation of p-Akt. Leukemia research. vol 64. 2018-11-05. PMID:29179029. |
we have previously used western blot analysis to show that the catalytic topoisomerase (topo) inhibitor, 3ez, 20ac-ingenol, induced dna damage response (ddr), which activated atr, downregulated p-akt through upregulation of pten level, and led to cell cycle arrest or apoptosis. |
2018-11-05 |
2023-08-13 |
Not clear |
| Shohei Miyata, Li-Yan Wang, Susumu Kitanak. 3EZ, 20Ac-ingenol induces cell-specific apoptosis in cyclin D1 over-expression through the activation of ATR and downregulation of p-Akt. Leukemia research. vol 64. 2018-11-05. PMID:29179029. |
in this study, we used atr or pten sirna and observed that the specific cell arrest and apoptosis of ball-1 cells in ddr caused by 3ez, 20ac-ingenol was dependant on activation of atr and downregulation of nuclear p-akt through upregulation of pten. |
2018-11-05 |
2023-08-13 |
Not clear |
| Li Wei, Shanshan Zhu, Jing Wang, Rong Quan, Xu Yan, Zixue Li, Lei Hou, Naidong Wang, Yi Yang, Haijun Jiang, Jue Li. Induction of a Cellular DNA Damage Response by Porcine Circovirus Type 2 Facilitates Viral Replication and Mediates Apoptotic Responses. Scientific reports. vol 6. 2018-06-19. PMID:27982097. |
cellular dna damage response (ddr) triggered by infection of dna viruses mediate cell cycle checkpoint activation, dna repair, or apoptosis induction. |
2018-06-19 |
2023-08-13 |
Not clear |
| Derek A Franklin, Yizhou He, Patrick L Leslie, Andrey P Tikunov, Nick Fenger, Jeffrey M Macdonald, Yanping Zhan. p53 coordinates DNA repair with nucleotide synthesis by suppressing PFKFB3 expression and promoting the pentose phosphate pathway. Scientific reports. vol 6. 2018-05-30. PMID:27901115. |
although previous studies have emphasized the importance of p53-dependent cell cycle arrest and apoptosis for tumor suppression, recent studies have suggested that other areas of p53 regulation, such as metabolism and dna damage repair (ddr), are also essential for p53-dependent tumor suppression. |
2018-05-30 |
2023-08-13 |
Not clear |
| Bryndon J Oleson, Aaron Naatz, Sarah C Proudfoot, Chay Teng Yeo, John A Corbet. Role of Protein Phosphatase 1 and Inhibitor of Protein Phosphatase 1 in Nitric Oxide-Dependent Inhibition of the DNA Damage Response in Pancreatic β-Cells. Diabetes. vol 67. issue 5. 2018-05-25. PMID:29444892. |
we have shown that nitric oxide, in a cell type-selective manner, inhibits the dna damage response (ddr) and, in doing so, protects β-cells from dna damage-induced apoptosis. |
2018-05-25 |
2023-08-13 |
Not clear |
| Bryndon J Oleson, Aaron Naatz, Sarah C Proudfoot, Chay Teng Yeo, John A Corbet. Role of Protein Phosphatase 1 and Inhibitor of Protein Phosphatase 1 in Nitric Oxide-Dependent Inhibition of the DNA Damage Response in Pancreatic β-Cells. Diabetes. vol 67. issue 5. 2018-05-25. PMID:29444892. |
these findings support a pp1-independent mechanism by which nitric oxide selectively impairs ddr signaling and protects β-cells from dna damage-induced apoptosis. |
2018-05-25 |
2023-08-13 |
Not clear |
| Dorota Piekna-Przybylska, Gaurav Sharma, Sanjay B Maggirwar, Robert A Bambar. Deficiency in DNA damage response, a new characteristic of cells infected with latent HIV-1. Cell cycle (Georgetown, Tex.). vol 16. issue 10. 2018-03-09. PMID:28388353. |
cells with inefficient ddr are more vulnerable to therapeutic approaches that target ddr, thereby raising dna damage to a threshold that triggers apoptosis. |
2018-03-09 |
2023-08-13 |
Not clear |
| Domenico Delia, Shuki Mizutan. The DNA damage response pathway in normal hematopoiesis and malignancies. International journal of hematology. vol 106. issue 3. 2018-03-08. PMID:28707218. |
at the heart of the ddr are the related signaling kinases atm, atr, and dna-pk, which regulate dna repair and associated events such as cell cycle checkpoints, chromatin remodeling, transcription, and ultimately apoptosis. |
2018-03-08 |
2023-08-13 |
Not clear |
| Wanwei Zheng, Zhongguang Luo, Jun Zhang, Pei Min, Wenshuai Li, Diannan Xu, Ziqiang Zhang, Panpan Xiong, Hong Liang, Jie Li. Neural precursor cell expressed, developmentally downregulated 8‑activating enzyme inhibitor MLN4924 sensitizes colorectal cancer cells to oxaliplatin by inducing DNA damage, G2 cell cycle arrest and apoptosis. Molecular medicine reports. vol 15. issue 5. 2018-02-16. PMID:28447739. |
it was demonstrated that mln4924 treatment induced the dna damage response (ddr) by inactivating cullin‑ring ubiquitin ligases, subsequently leading to cell cycle disturbance and apoptosis in crc cells. |
2018-02-16 |
2023-08-13 |
Not clear |
| Wanwei Zheng, Zhongguang Luo, Jun Zhang, Pei Min, Wenshuai Li, Diannan Xu, Ziqiang Zhang, Panpan Xiong, Hong Liang, Jie Li. Neural precursor cell expressed, developmentally downregulated 8‑activating enzyme inhibitor MLN4924 sensitizes colorectal cancer cells to oxaliplatin by inducing DNA damage, G2 cell cycle arrest and apoptosis. Molecular medicine reports. vol 15. issue 5. 2018-02-16. PMID:28447739. |
mln4924 treatment increased the oxaliplatin‑induced ddr, g2 cell cycle arrest and apoptosis. |
2018-02-16 |
2023-08-13 |
Not clear |
| Wanwei Zheng, Zhongguang Luo, Jun Zhang, Pei Min, Wenshuai Li, Diannan Xu, Ziqiang Zhang, Panpan Xiong, Hong Liang, Jie Li. Neural precursor cell expressed, developmentally downregulated 8‑activating enzyme inhibitor MLN4924 sensitizes colorectal cancer cells to oxaliplatin by inducing DNA damage, G2 cell cycle arrest and apoptosis. Molecular medicine reports. vol 15. issue 5. 2018-02-16. PMID:28447739. |
in conclusion, mln4924 treatment may sensitize crc cells to oxaliplatin treatment by inducing the ddr and increasing protein expression levels of p‑chk2, leading to g2 cell cycle arrest and apoptosis. |
2018-02-16 |
2023-08-13 |
Not clear |
| Steven Cupello, Christine Richardson, Shan Ya. Cell-free Xenopus egg extracts for studying DNA damage response pathways. The International journal of developmental biology. vol 60. issue 7-8-9. 2018-01-31. PMID:27160070. |
in response to a variety of dna replication stress or dna damaging agents, the dna damage response (ddr) pathways are triggered for cells to coordinate dna repair, cell cycle checkpoints, apoptosis, and senescence. |
2018-01-31 |
2023-08-13 |
xenopus_laevis |
| M Herbette, M G Mercier, F Michal, D Cluet, C Burny, G Yvert, V J Robert, F Palladin. The C. elegans SET-2/SET1 histone H3 Lys4 (H3K4) methyltransferase preserves genome stability in the germline. DNA repair. vol 57. 2017-12-26. PMID:28779964. |
these defects are not due to a failure to activate the dna damage response (ddr) that allows detection, signaling and repair of dna lesions, because cell cycle arrest and apoptosis, key components of this pathway, are efficiently induced in set-2 mutant animal. |
2017-12-26 |
2023-08-13 |
caenorhabditis_elegans |
| Lin Yang, Yinan Yuan, Chengyu Fu, Xuefen Xu, Jieying Zhou, Shuhao Wang, Lingyi Kong, Zhiyu Li, Qinglong Guo, Libin We. LZ-106, a novel analog of enoxacin, inducing apoptosis via activation of ROS-dependent DNA damage response in NSCLCs. Free radical biology & medicine. vol 95. 2017-12-19. PMID:27012423. |
interestingly, additional evidence in our findings revealed that ddr and apoptosis could be alleviated in the presence of ros scavenger n-acetyl-cysteine (nac), indicating ros-dependent ddr involvement in lz-106-induced apoptosis. |
2017-12-19 |
2023-08-13 |
mouse |
| Vinay Jain, Birajalaxmi Da. Global transcriptome profile reveals abundance of DNA damage response and repair genes in individuals from high level natural radiation areas of Kerala coast. PloS one. vol 12. issue 11. 2017-12-06. PMID:29161272. |
gene ontology analysis revealed majority of these differentially expressed genes are involved in dna damage response (ddr) signaling, dna repair, cell cycle arrest, apoptosis, histone/chromatin modification and immune response. |
2017-12-06 |
2023-08-13 |
human |