| Literature DB >> 26566869 |
Sabrina Forveille1,2,3,4, Heng Zhou1,2,3,4,5, Allan Sauvat1,2,3,4, Lucillia Bezu1,2,3,4,5, Kevin Müller1,2,3,4,5, Peng Liu1,2,3,4,5, Laurence Zitvogel5,6,7,8, Gérard Pierron9, Øystein Rekdal10,11, Oliver Kepp1,2,3,4, Guido Kroemer1,2,3,4,12,13.
Abstract
The oncolytic peptide LTX-315 has been designed for killing human cancer cells and turned out to stimulate anti-cancer immune responses when locally injected into tumors established in immunocompetent mice. Here, we investigated the question whether LTX-315 induces apoptosis or necrosis. Transmission electron microscopy or morphometric analysis of chromatin-stained tumor cells revealed that LTX-315 failed to induce apoptotic nuclear condensation and rather induced a necrotic phenotype. Accordingly, LTX-315 failed to stimulate the activation of caspase-3, and inhibition of caspases by means of Z-VAD-fmk was unable to reduce cell killing by LTX-315. In addition, 2 prominent inhibitors of regulated necrosis (necroptosis), namely, necrostatin-1 and cycosporin A, failed to reduce LTX-315-induced cell death. In conclusion, it appears that LTX-315 triggers unregulated necrosis, which may contribute to its pro-inflammatory and pro-immune effects.Entities:
Keywords: anticancer immunity, apoptotsis, necrosis, LTX-315
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Year: 2015 PMID: 26566869 PMCID: PMC4825625 DOI: 10.1080/15384101.2015.1093710
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534