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Feasibility of using NF1-GRD and AAV for gene replacement therapy in NF1-associated tumors.

ABSTRACT: Neurofibromatosis type 1, including the highly aggressive malignant peripheral nerve sheath tumors (MPNSTs), is featured by the loss of functional neurofibromin 1 (NF1) protein resulting from genetic alterations. A major function of NF1 is suppressing Ras activities, which is conveyed by an intrinsic GTPase-activating protein-related domain (GRD). In this study, we explored the feasibility of restoring Ras GTPase via exogenous expression of various GRD constructs, via gene delivery using a panel of adeno-associated virus (AAV) vectors in MPNST and human Schwann cells (HSCs). We demonstrated that several AAV serotypes achieved favorable transduction efficacies in those cells and a membrane-targeting GRD fused with an H-Ras C-terminal motif (C10) dramatically inhibited the Ras pathway and MPNST cells in a NF1-specific manner. Our results opened up a venue of gene replacement therapy in NF1-related tumors.

SUBMITTER: Bai RY

PROVIDER: S-EPMC6588423 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Feasibility of using NF1-GRD and AAV for gene replacement therapy in NF1-associated tumors.

Bai Ren-Yuan RY Esposito Dominic D Tam Ada J AJ McCormick Frank F Riggins Gregory J GJ Wade Clapp D D Staedtke Verena V

Gene therapy 20190524 6

Neurofibromatosis type 1, including the highly aggressive malignant peripheral nerve sheath tumors (MPNSTs), is featured by the loss of functional neurofibromin 1 (NF1) protein resulting from genetic alterations. A major function of NF1 is suppressing Ras activities, which is conveyed by an intrinsic GTPase-activating protein-related domain (GRD). In this study, we explored the feasibility of restoring Ras GTPase via exogenous expression of various GRD constructs, via gene delivery using a panel ...[more]

PMID: 31127187

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