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The novel atypical retinoid ST5589 down-regulates Aurora Kinase A and has anti-tumour activity in lymphoma pre-clinical models.
- Source :
-
British journal of haematology [Br J Haematol] 2015 Nov; Vol. 171 (3), pp. 378-86. Date of Electronic Publication: 2015 Aug 03. - Publication Year :
- 2015
-
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.<br /> (© 2015 John Wiley & Sons Ltd.)
- Subjects :
- Apoptosis drug effects
Cell Line, Tumor
Drug Screening Assays, Antitumor
Humans
Lymphoma enzymology
Lymphoma pathology
Aurora Kinase A biosynthesis
Down-Regulation drug effects
Gene Expression Regulation, Enzymologic drug effects
Gene Expression Regulation, Neoplastic drug effects
Lymphoma drug therapy
Neoplasm Proteins biosynthesis
Retinoids pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1365-2141
- Volume :
- 171
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- British journal of haematology
- Publication Type :
- Academic Journal
- Accession number :
- 26235926
- Full Text :
- https://doi.org/10.1111/bjh.13595