Title : Transcription-independent and -dependent p53-mediated apoptosis in response to genotoxic and non-genotoxic stress.

Pub. Date : 2019

PMID : 31482012






3 Functional Relationships(s)
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1 In addition to doxorubicin, our results here indicated that camptothecin and bortezomib, which are a topoisomerase 1 poison and a 26 S proteasome inhibitor, respectively, could also induce apoptosis in a p53-dependent manner in prostate cancer. Bortezomib tumor protein p53 Homo sapiens
2 In contrast, p53-mediated apoptosis from bortezomib-induced stress is transcription-dependent. Bortezomib tumor protein p53 Homo sapiens
3 We then investigated the p53 ratio of nucleus to cytosol corresponding to low and high dose doxorubicin, camptothecin, or bortezomib treatment. Bortezomib tumor protein p53 Homo sapiens