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The PLK4 inhibitor RP-1664 demonstrates potent efficacy in neuroblastoma preclinical models through a dual mechanism of sensitivity

  • Isabel Soria-Bretones,
  • Matias Casás-Selves,
  • Minu Samanta,
  • David Groff,
  • Jayne Murray,
  • Jamie I. Fletcher,
  • Alvin Farrel,
  • Steven Pastor,
  • Khushbu Patel,
  • Elliot Goodfellow,
  • Li Li,
  • Cathy Caron,
  • Ariya Shiwram,
  • Hyeyeon Kim,
  • Danielle Henry,
  • Nancy Laterreur,
  • Julian Bowlan,
  • Kateryna Krytska,
  • Steven B. Neuhauser,
  • Timothy M. Stearns,
  • Jeffrey A. Schubert,
  • Jinhua Wu,
  • Lea F. Surrey,
  • Daniel Martinez,
  • Crystal Mak,
  • Jennifer Brand,
  • Caitlin Wesley,
  • Klaartje Somers,
  • Alejandro Álvarez-Quilón,
  • Frédéric Vallée,
  • Parham Nejad,
  • Joseph D. Schonhoft,
  • Joanna Li,
  • Artur Veloso,
  • Jordan T. F. Young,
  • Marc L. Hyer,
  • Stephen J. Morris,
  • Yael P. Mossé,
  • C. Gary Marshall,
  • Michelle Haber,
  • Michal Zimmermann,
  • John M. Maris

摘要

It was recently shown that inhibition of polo-like kinase 4 (PLK4) induces synthetic lethality in cancers with chromosome 17q-encoded TRIM37 copy number gain due to cooperative regulation of centriole duplication and mitotic spindle nucleation. We show here that chromosome 17q/TRIM37 gain is a defining feature of high-risk neuroblastoma and renders patient-derived cell lines hypersensitive to the novel PLK4 inhibitor RP-1664. We demonstrate that centriole amplification at low doses of RP-1664 contributes to this sensitivity in a TRIM37-independent fashion. CRISPR screens and live cell imaging reveal that upon centriole amplification, neuroblastoma cells succumb to multipolar mitoses due to an inability to cluster or inactivate supernumerary centrosomes. RP-1664 monotherapy showed robust anti-tumor activity in 14/15 human neuroblastoma-derived xenograft models, and significantly extended survival in a transgenic MYCN-driven murine model of neuroblastoma. RP-1664 combined with GD2-directed chemoimmunotherapy resulted in maintained complete responses in 6/9 mice with established MYCN-driven murine neuroblastomas. These data support clinical development of PLK4 inhibitors for high-risk neuroblastoma and other cancers with somatically acquired TRIM37 overexpression.