FCCC LOGO Faculty Publications
Hawley E , Gehlhausen J , Karchugina S , Chow HY , Araiza-Olivera D , Radu M , Smith A , Burks C , Jiang L , Li X , Bessler W , Masters A , Edwards D , Burgin C , Jones D , Yates C , Clapp DW , Chernoff J , Park SJ
PAK1 inhibition reduces tumor size and extends the lifespan of mice in a genetically engineered mouse model of Neurofibromatosis Type 2 (NF2)
Hum Mol Genet. 2021 Jun 1
PMID: 34075397    PMCID: PMC8369838    URL: https://www.ncbi.nlm.nih.gov/pubmed/34075397
Back to previous list
Abstract
Neurofibromatosis Type II (NF2) is an autosomal dominant cancer predisposition syndrome in which germline haploinsufficiency at the NF2 gene confers a greatly increased propensity for tumor development arising from tissues of neural crest derived origin. NF2 encodes the tumor suppressor, Merlin, and its biochemical function is incompletely understood. One well established function of Merlin is as a negative regulator of group A serine/threonine p21 activated kinases (PAKs). In these studies we explore the role of PAK1 and its closely related paralog, PAK2, both pharmacologically and genetically, in Merlin deficient Schwann cells and in a genetically engineered mouse model (GEMM) that develops spontaneous vestibular and spinal schwannomas. We demonstrate that PAK1 and PAK2 are both hyper activated in Merlin deficient murine schwannomas. In preclinical trials, a pan Group A PAK inhibitor, FRAX-1036, transiently reduced PAK1 and PAK2 phosphorylation in vitro, but had insignificant efficacy in vivo. NVS-PAK1-1, a PAK1 selective inhibitor, had a greater but still minimal effect on our GEMM phenotype. However, genetic ablation of Pak1 but not Pak2 reduced tumor formation in our NF2 GEMM. Moreover, germline genetic deletion of Pak1 was well tolerated while conditional deletion of Pak2 in Schwann cells resulted in significant morbidity and mortality. These data support the further development of PAK1-specific small molecule inhibitors and the therapeutic targeting of PAK1 in vestibular schwannomas and argue against PAK1 and PAK2 existing as functionally redundant protein isoforms in Schwann cells.
Notes
1460-2083 Hawley, Eric Gehlhausen, Jeffrey Karchugina, Sofiia Chow, Hoi-Yee Araiza-Olivera, Daniela Radu, Maria Smith, Abbi Burks, Ciersten Jiang, Li Li, Xiaohong Bessler, Waylan Masters, Andrea Edwards, Donna Burgin, Callie Jones, David Yates, Charles Clapp, D Wade Chernoff, Jonathan Park, Su-Jung Journal Article England Hum Mol Genet. 2021 Jun 1:ddab106. doi: 10.1093/hmg/ddab106.