Nucleolin antagonist triggers autophagic cell death in human glioblastoma primary cells and decreased in vivo tumor growth in orthotopic brain tumor model
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Elisabetta Benedetti1,*, Andrea Antonosante1,*, Michele d’Angelo1, Loredana Cristiano1, Renato Galzio1, Damien Destouches2,3, Tiziana Marilena Florio1, Anne Chloé Dhez1, Carlo Astarita6, Benedetta Cinque1, Alessia Fidoamore1, Floriana Rosati4, Maria Grazia Cifone1, Rodolfo Ippoliti1, Antonio Giordano5,6, José Courty2,3, Annamaria Cimini1,6,7
1Department of Life, Health and Environmental Sciences, University of L’Aquila, L’Aquila, Italy
2Department of Cell Biology, Université Paris-Est, UPEC, Créteil, France
3Laboratoire de Recherche sur la Croissance Cellulaire, la Réparation et la Régénération Tissulaires (CRRET) CNRS, Créteil, France
4Department of Life Sciences, University of Siena, Siena, Italy
5Department of Medicine, Surgery and Neuroscience, University of Siena, Siena, Italy
6Sbarro Institute for Cancer Research and Molecular Medicine and Center for Biotechnology, Temple University, Philadelphia, Pennsylvania, USA
7National Institute for Nuclear Physics (INFN), Gran Sasso National Laboratory (LNGS), Assergi, Italy
*These authors have contributed equally to this work
Annamaria Cimini, e-mail: [email protected]
José Courty, e-mail: courty@u-pec-fr
Keywords: glioblastoma, autophagy, targeted therapy
Received: July 15, 2015 Accepted: October 09, 2015 Published: October 19, 2015
Nucleolin (NCL) is highly expressed in several types of cancer and represents an interesting therapeutic target. It is expressed at the plasma membrane of tumor cells, a property which is being used as a marker for several human cancer including glioblastoma. In this study we investigated targeting NCL as a new therapeutic strategy for the treatment of this pathology. To explore this possibility, we studied the effect of an antagonist of NCL, the multivalent pseudopeptide N6L using primary culture of human glioblastoma cells. In this system, N6L inhibits cell growth with different sensitivity depending to NCL localization. Cell cycle analysis indicated that N6L-induced growth reduction was due to a block of the G1/S transition with down-regulation of the expression of cyclin D1 and B2. By monitoring autophagy markers such as p62 and LC3II, we demonstrate that autophagy is enhanced after N6L treatment. In addition, N6L-treatment of mice bearing tumor decreased in vivo tumor growth in orthotopic brain tumor model and increase mice survival. The results obtained indicated an anti-proliferative and pro-autophagic effect of N6L and point towards its possible use as adjuvant agent to the standard therapeutic protocols presently utilized for glioblastoma.
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