PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 31607444-5 2019 In contrast, P53 induction by Nutlin and Hsp90 inhibitor AUY922 enhanced the BBB function. nutlin 30-36 tumor protein p53 Homo sapiens 13-16 33216890-2 2020 There is concern, however, that nutlin therapy might stimulate the emergence or expansion of TP53-mutated subclones. nutlin 32-38 tumor protein p53 Homo sapiens 93-97 24366007-11 2014 Collectively, these results suggest that nutlin-3 induces HO-1 expression via the activation of both JNK which is dependent on ROS generated by p53 translocated to the mitochondria and p38 MAPK which appears to be stimulated by a ROS-independent mechanism, and this HO-1 induction may inhibit nutlin-3-induced apoptosis, constituting a negative feedback loop of p53-induced apoptosis. nutlin 41-47 tumor protein p53 Homo sapiens 144-147 26883108-7 2016 In addition, combined treatment with GSK2830371 and doxorubicin or nutlin-3 potentiated cell death through a strong induction of p53 pathway and activation of caspase 9. nutlin 67-73 tumor protein p53 Homo sapiens 129-132 24885082-3 2014 In this study we aimed to investigate the functional role of this p53 acetylation in nutlin-sensitivity, and further to explore if nutlin-induced protein acetylation in general could indicate novel targets for the enhancement of nutlin-based therapy. nutlin 85-91 tumor protein p53 Homo sapiens 66-69 29932882-9 2018 After treatment with Nutlin, increased nuclear localization of p53 (4.05%-80.56%) was observed in pterygium cells along with increasing Nutlin dosages (from 0 to 50 muM, p < 0.001). nutlin 21-27 tumor protein p53 Homo sapiens 63-66 24366007-11 2014 Collectively, these results suggest that nutlin-3 induces HO-1 expression via the activation of both JNK which is dependent on ROS generated by p53 translocated to the mitochondria and p38 MAPK which appears to be stimulated by a ROS-independent mechanism, and this HO-1 induction may inhibit nutlin-3-induced apoptosis, constituting a negative feedback loop of p53-induced apoptosis. nutlin 41-47 tumor protein p53 Homo sapiens 362-365 20871630-8 2011 p21 was found to mediate nutlin-induced p53-dependent downregulation of another antiapoptotic protein, survivin, without significantly affecting the apoptotic outcome. nutlin 25-31 tumor protein p53 Homo sapiens 40-43 23856246-5 2013 Furthermore, we identify pharmacogenomic correlations between specific variants in genes such as TP53, BRAF, ERBBs, and ATAD5 and anticancer agents such as nutlin, vemurafenib, erlotinib, and bleomycin showing one of many ways the data could be used to validate and generate novel hypotheses for further investigation. nutlin 156-162 tumor protein p53 Homo sapiens 97-101 22578852-11 2012 From these results, we concluded that nutlin-3 has an antitumor effect on feline lymphoma cell lines harboring the wt-p53 gene through accumulation and activation of P53 leading to cell cycle arrest and apoptosis. nutlin 38-44 tumor protein p53 Homo sapiens 118-121 22578852-11 2012 From these results, we concluded that nutlin-3 has an antitumor effect on feline lymphoma cell lines harboring the wt-p53 gene through accumulation and activation of P53 leading to cell cycle arrest and apoptosis. nutlin 38-44 tumor protein p53 Homo sapiens 166-169 19509161-12 2009 A combination of vincristine or actinomycin D with nutlin-3 enhanced the antitumor activity in RMS cell lines with wild-type p53. nutlin 51-57 tumor protein p53 Homo sapiens 125-128 20371712-3 2010 Previous studies have reported that Nutlin promotes growth arrest and/or apoptosis in cancer cells that express wild-type p53. nutlin 36-42 tumor protein p53 Homo sapiens 122-125 20371712-9 2010 Taken together, these findings reveal that Nutlin treatment can inhibit the migration and invasion capacity of p53 wild-type cells, adding to the potential therapeutic benefit of Nutlin and other small molecule MDM2 inhibitors. nutlin 43-49 tumor protein p53 Homo sapiens 111-114 20424123-10 2010 In contrast, doxorubicin or nutlin-3 treatment-both leading to p53-p21 activation-or CDK2 inhibition had no effect on SKP2 regulation in MYCN-amplified cells. nutlin 28-34 tumor protein p53 Homo sapiens 63-66 19190243-4 2009 Of note, Nutlin-3 up-regulated Notch1 expression also in primary TP53(wild-type) B-chronic lymphocytic leukemia (B-CLL) cells and the combined use of Nutlin-3 plus pharmacological gamma-secretase inhibitors of the Notch signaling showed a synergistic cytotoxicity in both TP53(wild-type) leukemic cell lines and primary B-CLL cells. nutlin 9-15 tumor protein p53 Homo sapiens 65-69 19411846-10 2009 Surprisingly, blocking the transcriptional arm of p53, either via alpha-Amanitin or the p53-specific transcriptional inhibitor Pifithrin alpha, not only fails to inhibit, but greatly potentiates Nutlin-induced apoptosis. nutlin 195-201 tumor protein p53 Homo sapiens 50-53 19411846-10 2009 Surprisingly, blocking the transcriptional arm of p53, either via alpha-Amanitin or the p53-specific transcriptional inhibitor Pifithrin alpha, not only fails to inhibit, but greatly potentiates Nutlin-induced apoptosis. nutlin 195-201 tumor protein p53 Homo sapiens 88-91 19190243-4 2009 Of note, Nutlin-3 up-regulated Notch1 expression also in primary TP53(wild-type) B-chronic lymphocytic leukemia (B-CLL) cells and the combined use of Nutlin-3 plus pharmacological gamma-secretase inhibitors of the Notch signaling showed a synergistic cytotoxicity in both TP53(wild-type) leukemic cell lines and primary B-CLL cells. nutlin 9-15 tumor protein p53 Homo sapiens 272-276