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PDLIM7 and CDH18 regulate the turnover of MDM2 during CDK4/6 inhibitor therapy-induced senescence

  • Mary E. Klein
  • , Mark A. Dickson
  • , Cristina Antonescu
  • , Li Xuan Qin
  • , Scott J. Dooley
  • , Afsar Barlas
  • , Katia Manova
  • , Gary K. Schwartz
  • , Aimee M. Crago
  • , Samuel Singer
  • , Andrew Koff
  • , William D. Tap

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

CDK4/6 inhibitors are being used to treat a variety of human malignancies. In well-differentiated and dedifferentiated liposarcoma their clinical promise is associated with their ability to downregulate the MDM2 protein. The downregulation of MDM2 following treatment with CDK4/6 inhibitors also induces many cultured tumor cell lines derived from different types of malignancies to progress from quiescence into senescence. Here we used cultured human cell lines and defined a role for PDLIM7 and CDH18, regulating MDM2 protein in CDK4/6 inhibitor-treated cells. Materials from our previous phase II trials with palbociclib were then used to demonstrate that expression of CDH18 protein was associated with response, measured as both progression-free survival and overall survival. This supports the hypothesis that the biologic transition from quiescence to senescence has clinical relevance for this class of drugs.

Original languageEnglish
Pages (from-to)5066-5078
Number of pages13
JournalOncogene
Volume37
Issue number37
DOIs
StatePublished - 13 Sep 2018
Externally publishedYes

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