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The HSP70 Modulator MAL3-101 Inhibits Merkel Cell Carcinoma

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-112795
  • Merkel Cell Carcinoma (MCC) is a rare and highly aggressive neuroendocrine skin cancer for which no effective treatment is available. MCC represents a human cancer with the best experimental evidence for a causal role of a polyoma virus. Large T antigens (LTA) encoded by polyoma viruses are oncoproteins, which are thought to require support of cellular heat shock protein 70 (HSP70) to exert their transforming activity. Here we evaluated the capability of MAL3-101, a synthetic HSP70 inhibitor, to limit proliferation and survival of various MCCMerkel Cell Carcinoma (MCC) is a rare and highly aggressive neuroendocrine skin cancer for which no effective treatment is available. MCC represents a human cancer with the best experimental evidence for a causal role of a polyoma virus. Large T antigens (LTA) encoded by polyoma viruses are oncoproteins, which are thought to require support of cellular heat shock protein 70 (HSP70) to exert their transforming activity. Here we evaluated the capability of MAL3-101, a synthetic HSP70 inhibitor, to limit proliferation and survival of various MCC cell lines. Remarkably, MAL3-101 treatment resulted in considerable apoptosis in 5 out of 7 MCC cell lines. While this effect was not associated with the viral status of the MCC cells, quantitative mRNA expression analysis of the known HSP70 isoforms revealed a significant correlation between MAL3-101 sensitivity and HSC70 expression, the most prominent isoform in all cell lines. Moreover, MAL3-101 also exhibited in vivo antitumor activity in an MCC xenograft model suggesting that this substance or related compounds are potential therapeutics for the treatment of MCC in the future.zeige mehrzeige weniger

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Metadaten
Autor(en): Christian Adam, Anne Baeurle, Jeffrey L. Brodsky, David Schrama, Peter Wipf, Jürgen Christian Becker, Roland Houben
URN:urn:nbn:de:bvb:20-opus-112795
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Klinik und Poliklinik für Dermatologie, Venerologie und Allergologie
Sprache der Veröffentlichung:Englisch
Erscheinungsjahr:2014
Originalveröffentlichung / Quelle:PLoS ONE 9(4): e92041. doi:10.1371/journal.pone.0092041
DOI:https://doi.org/10.1371/journal.pone.0092041
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):apoptosis; cancer treatment; cell staining; cultured fibroplasts; heat shock response; membrans proteins; polymerase chain reaction
Datum der Freischaltung:13.05.2015
Sammlungen:Open-Access-Publikationsfonds / Förderzeitraum 2014
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung