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Resistance to caspase-8 and -9 fragments in a malignant pleural mesothelioma cell line with acquired cisplatin-resistance.
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk biovetenskap, Klinisk kemi.
Umeå universitet, Medicinska fakulteten, Institutionen för odontologi.
Umeå universitet, Medicinska fakulteten, Institutionen för medicinsk biovetenskap, Klinisk kemi.
2010 (engelsk)Inngår i: Cell death & disease, ISSN 2041-4889, Vol. 1, nr 9, s. e78-Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Apoptotic cysteine-aspartate proteases (caspases) are essential for the progression and execution of apoptosis, and detection of caspase fragmentation or activity is often used as markers of apoptosis. Cisplatin (cis-diamminedichloroplatinum (II)) is a chemotherapeutic drug that is clinically used for the treatment of solid tumours. We compared a cisplatin-resistant pleural malignant mesothelioma cell line (P31res1.2) with its parental cell line (P31) regarding the consequences of in vitro acquired cisplatin-resistance on basal and cisplatin-induced (equitoxic and equiapoptotic cisplatin concentrations) caspase-3, -8 and -9 fragmentation and proteolytic activity. Acquisition of cisplatin-resistance resulted in basal fragmentation of caspase-8 and -9 without a concomitant increase in proteolytic activity, and there was an increased basal caspase-3/7 activity. Similarly, cisplatin-resistant non-small-cell lung cancer cells, H1299res, had increased caspase-3 and -9 content compared with the parental H1299 cells. In P31 cells, cisplatin exposure resulted in caspase-9-mediated caspase-3/7 activation, but in P31res1.2 cells the cisplatin-induced caspase-3/7 activation occurred before caspase-8 or -9 activation. We therefore concluded that in vitro acquisition of cisplatin-resistance rendered P31res1.2 cells resistant to caspase-8 and caspase-9 fragments and that cisplatin-induced, initiator-caspase independent caspase-3/7 activation was necessary to overcome this resistance. Finally, the results demonstrated that detection of cleaved caspase fragments alone might be insufficient as a marker of caspase activity and ensuing apoptosis induction.

sted, utgiver, år, opplag, sider
Nature Publishing Group , 2010. Vol. 1, nr 9, s. e78-
Emneord [en]
caspase fragmentation, caspase activity, cisplatin-resistance, malignant pleural mesothelioma
HSV kategori
Forskningsprogram
cellforskning
Identifikatorer
URN: urn:nbn:se:umu:diva-40650DOI: 10.1038/cddis.2010.54ISI: 000282361700010PubMedID: 21364680OAI: oai:DiVA.org:umu-40650DiVA, id: diva2:404978
Tilgjengelig fra: 2011-03-19 Laget: 2011-03-03 Sist oppdatert: 2018-06-08bibliografisk kontrollert

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