| Literature DB >> 17084521 |
Martin Michaelis1, Jaroslav Cinatl, Puja Anand, Florian Rothweiler, Rouslan Kotchetkov, Andreas von Deimling, Hans W Doerr, Kuslima Shogen, Jindrich Cinatl.
Abstract
The efficacy of Onconase on the growth of a panel of chemosensitive and chemoresistant neuroblastoma cell lines was investigated. Onconase decreased cell viability of chemosensitive (IMR-32, UKF-NB-3) and chemoresistant neuroblastoma cell lines characterised by high expression of P-glycoprotein (P-gp) (UKF-NB-3(r)DOX(20)) or by high P-gp expression in combination with mutated p53 (UKF-NB-3(r)VCR(10), Be(2)-C), in a similar manner. Moreover, Onconase caused cell cycle block in G1 phase and induced caspase-independent cell death. Transmission electron microscope investigations suggested that Onconase-induced autophagy contributes to Onconase-induced cell death. Antitumour activity of Onconase against naïve and drug-resistant neuroblastoma xenografts was confirmed in animals.Entities:
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Year: 2006 PMID: 17084521 DOI: 10.1016/j.canlet.2006.09.018
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679