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Proteasome inhibitor PSI induces apoptosis in human mesothelioma cells
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Genetics and Pathology.
2006 (English)In: Cancer Letters, ISSN 0304-3835, E-ISSN 1872-7980, Vol. 232, no 2, 161-169 p.Article in journal (Refereed) Published
Abstract [en]

Malignant mesothelioma is an increasingly common tumor with an almost 100% mortality rate. It is refractory to conventional treatment. We have previously shown with SSH and microarray that the mRNA expression level of proteasome is higher in epithelioid mesothelioma cell lines than in sarcomatoid ones. This study evaluates the differential apoptotic effect of proteasome inhibitors on both of these mesothelioma sub-lines. Proteasome inhibitors show substantial anti-tumor activity in some tumor cells in vitro and in vivo, but the effects on mesothelioma cells has not been studied. The viability of mesothelioma cells was reduced in a dose- and time-dependent manner by the proteasome inhibitors tested; PSI was effective with a low dose, but higher concentrations were needed for calpain inhibitor I. The epithelioid mesothelioma cells are more sensitive to the inhibitors than the sarcomatoid ones, their IC50 after 24 h of treatment with PSI being 4 and 16 microm, respectively. Other mesothelioma cell lines show similar sensitivity. PSI seemed to decrease mesothelioma viability by inducing apoptosis, as verified by cell morphology, Western blotting analysis of caspase 3 cleavage, and flow-cytometric analysis. In conclusion, PSI, a representative agent that reduces viability and induces apoptosis of mesothelioma cells, might be useful in the treatment of patients with mesothelioma, especially of epithelioid phenotype.

Place, publisher, year, edition, pages
2006. Vol. 232, no 2, 161-169 p.
National Category
Dermatology and Venereal Diseases Cell and Molecular Biology
Research subject
Dermatology and Venerology; Pathology
URN: urn:nbn:se:uu:diva-125868DOI: 10.1016/j.canlet.2005.02.022PubMedID: 16458112OAI: oai:DiVA.org:uu-125868DiVA: diva2:321116
Available from: 2010-05-28 Created: 2010-05-28 Last updated: 2010-07-13Bibliographically approved

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