Research Papers:
Co-targeting the MAPK and PI3K/AKT/mTOR pathways in two genetically engineered mouse models of schwann cell tumors reduces tumor grade and multiplicity
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Abstract
Adrienne L. Watson1,2,3,4,*, Bryant J. Keller1,2,3,4,*, Kyle A. Williams1,2,3,4, Namrata N. Damle1,2,3,4, Samuel J. Finnerty1,2,3,4, Leah K. Anderson1,2, Andrew D. Greeley1,2, Vincent W. Keng1,2,3,4,10, Eric P. Rahrmann1,2,3,4, Amanda L. Halfond5, Natasha M. Powell4, Margaret H. Collins8, Tilat Rizvi8, Christopher L. Moertel6, Nancy Ratner7,9, and David A. Largaespada1,2,3,4,6
1 Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA
2 Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN, USA
3 Center for Genome Engineering, University of Minnesota, Minneapolis, MN, USA
4 Brain Tumor Program, University of Minnesota, Minneapolis, MN, USA
5 Health and Natural Sciences Department, University of Minnesota, Minneapolis, MN, USA
6 Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA
7 Division of Experimental Hematology and Cancer Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
8 Division of Pathology and Laboratory Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
9 Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, USA
10 Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong.
* These two authors contributed equally to this work
Correspondence:
David A. Largaespada, email:
Keywords: Malignant peripheral nerve sheath tumors, plexiform neurofibromas, Schwann cells, neurofibromatosis type 1 syndrome, neurofibromin 1, PI3K/AKT/mTOR signaling, MAPK signaling, targeted therapies, genetically engineered mouse models, combination therapy
Received: November 18, 2013 Accepted: January 18, 2014 Published: January 20, 2014
Abstract
Malignant peripheral nerve sheath tumors (MPNSTs) are soft tissue sarcomas that occur spontaneously, or from benign plexiform neurofibromas, in the context of the genetic disorder Neurofibromatosis Type 1 (NF1). The current standard treatment includes surgical resection, high-dose chemotherapy, and/or radiation. To date, most targeted therapies have failed to demonstrate effectiveness against plexiform neurofibromas and MPNSTs. Recently, several studies suggested that the mTOR and MAPK pathways are involved in the formation and progression of MPNSTs. Everolimus (RAD001) inhibits the mTOR and is currently FDA approved for several types of solid tumors. PD-0325901 (PD-901) inhibits MEK, a component of the MAPK pathway, and is currently in clinical trials. Here, we show in vitro than MPNST cell lines are more sensitive to inhibition of cellular growth by Everolimus and PD-901 than immortalized human Schwann cells. In combination, these drugs synergistically inhibit cell growth and induce apoptosis. In two genetically engineered mouse models of MPNST formation, modeling both sporadic and NF1-associated MPNSTs, Everolimus, or PD-901 treatment alone each transiently reduced tumor burden and size, and extended lifespan. However, prolonged treatment of each single agent resulted in the development of resistance and reactivation of target pathways. Combination therapy using Everolimus and PD-901 had synergistic effects on reducing tumor burden and size, and increased lifespan. Combination therapy allowed persistent and prolonged reduction in signaling through both pathways. These data suggest that co-targeting mTOR and MEK may be effective in patients with sporadic or NF1-associated MPNSTs.
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