| Literature DB >> 26235926 |
Elena Bernasconi1, Eugenio Gaudio1, Ivo Kwee1,2,3, Andrea Rinaldi1, Luciano Cascione1,4, Chiara Tarantelli1, Afua Adjeiwaa Mensah1, Anastasios Stathis4, Emanuele Zucca4, Loredana Vesci5, Giuseppe Giannini5, Francesco Bertoni1,4.
Abstract
Despite the marked improvements in the treatment of lymphomas, there is still a need for new therapeutic agents. Synthetic retinoids represent a class of compounds with anti-cancer activity. Here, we report the preclinical activity of a new member of this class, the ST1926-derivative ST5589, in lymphomas. ST5589 presented a dose-dependent anti-proliferative activity in almost all of the 25 lymphoma cell lines analysed, with a median 50% inhibitory concentration of 433 nM. Apoptosis was observed in 8/11 cell lines. ST5589 induced changes in the gene expression profiles of the cell lines, including the down-regulation of Aurora Kinase A (AURKA). Specific gene expression signatures were associated with a higher sensitivity to the compound and combination of ST5589 with carfilzomib revealed the importance of proteasome activity in mediating the anti-tumour activity of ST5589. In conclusion, we have identified a new mechanism of action of atypical retinoids as anti-cancer compounds, and the encouraging results obtained with the new ST1926-derivative ST5589 provide the basis for further developments of the compound.Entities:
Keywords: MYC; ST1926; aurora kinase; lymphomas; new drugs for lymphoma; retinoids
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Year: 2015 PMID: 26235926 DOI: 10.1111/bjh.13595
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998