Pharmacogenomic synthetic lethal screens reveal hidden vulnerabilities and new therapeutic approaches for treatment of NF1-associated tumors.

Autor:	Williams KB; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA., Larsson AT; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA., Keller BJ; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA., Chaney KE; Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, 45229-0713, USA., Williams RL; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA., Bhunia MM; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.; Department of Genetics, Cell Biology and Development, University of Minnesota, Twin Cities, Minneapolis, Minnesota 55455, USA., Draper GM; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA., Jubenville TA; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA., Hudson WA; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA., Moertel CL; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA., Ratner N; Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, 45229-0713, USA., Largaespada DA; Department of Pediatrics, Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.; Department of Genetics, Cell Biology and Development, University of Minnesota, Twin Cities, Minneapolis, Minnesota 55455, USA.
Jazyk:	angličtina
Zdroj:	BioRxiv : the preprint server for biology [bioRxiv] 2024 Nov 01. Date of Electronic Publication: 2024 Nov 01.
DOI:	10.1101/2024.03.25.585959
Abstrakt:	Neurofibromatosis Type 1 (NF1) is a common cancer predisposition syndrome, caused by heterozygous loss of function mutations in the tumor suppressor gene NF1 . Individuals with NF1 develop benign tumors of the peripheral nervous system (neurofibromas), originating from the Schwann cell linage after somatic loss of the wild type NF1 allele, some of which progress further to malignant peripheral nerve sheath tumors (MPNST). There is only one FDA approved targeted therapy for symptomatic plexiform neurofibromas and none approved for MPNST. The genetic basis of NF1 syndrome makes associated tumors ideal for using synthetic drug sensitivity approaches to uncover therapeutic vulnerabilities. We developed a drug discovery pipeline to identify therapeutics for NF1-related tumors using isogeneic pairs of NF1- proficient and deficient immortalized human Schwann cells. We utilized these in a large-scale high throughput screen (HTS) for drugs that preferentially kill NF1 -deficient cells, through which we identified 23 compounds capable of killing NF1- deficient Schwann cells with selectivity. Multiple hits from this screen clustered into classes defined by method of action. Four clinically interesting drugs from these classes were tested in vivo using both a genetically engineered mouse model of high-grade peripheral nerve sheath tumors and human MPNST xenografts. All drugs tested showed single agent efficacy in these models as well as significant synergy when used in combination with the MEK inhibitor Selumetinib. This HTS platform yielded novel therapeutically relevant compounds for the treatment of NF1-associated tumors and can serve as a tool to rapidly evaluate new compounds and combinations in the future. Competing Interests: Conflicts of Interest: D.A.L. is the co-founder and co-owner of NeoClone Biotechnologies, Inc., Discovery Genomics, Inc. (acquired by Immunsoft, Inc.), B-MoGen Biotechnologies, Inc. (acquired by Bio-Techne corporation), and Luminary Therapeutics, Inc. D.A.L. holds equity in, is on the Board of Directors of, and serves as a Senior Scientific Advisor to Recombinetics, a genome-editing company. He consults for and has equity in Styx Biotechnologies, Inc. and Genentech, Inc., which is funding some of his research. The business of all the companies above is unrelated to the contents of this manuscript. N.R. had research support from Boehringer Ingelheim, Revolution Medicines, and Healx during the course of this study, unrelated to these studies. Other authors have no conflicts of interest to disclose.
Databáze:	MEDLINE
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