Cell Death and Disease (Nov 2024)

Aurora B inhibitors promote RB hypophosphorylation and senescence independent of p53-dependent CDK2/4 inhibition

  • Shivam Vora,
  • Ariel Andrew,
  • Ramyashree Prasanna Kumar,
  • Deborah Nazareth,
  • Alexis Bonfim-Melo,
  • Yoon Lim,
  • Xin Yee Ong,
  • Madushan Fernando,
  • Yaowu He,
  • John D. Hooper,
  • Nigel AJ McMillan,
  • Jelena Urosevic,
  • Jon Travers,
  • Jamal Saeh,
  • Sharad Kumar,
  • Mathew JK Jones,
  • Brian Gabrielli

DOI
https://doi.org/10.1038/s41419-024-07204-5
Journal volume & issue
Vol. 15, no. 11
pp. 1 – 9

Abstract

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Abstract Aurora B kinase (AURKB) inhibitors have been trialled in a range of different tumour types but are not approved for any indication. Expression of the human papilloma virus (HPV) oncogenes and loss of retinoblastoma (RB) protein function has been reported to increase sensitivity to AURKB inhibitors but the mechanism of their contribution to sensitivity is poorly understood. Two commonly reported outcomes of AURKB inhibition are polyploidy and senescence, although their relationship is unclear. Here we have investigated the major cellular targets of the HPV E6 and E7, p53 and RB, to determine their contribution to AURKB inhibitor induced polyploidy and senescence. We demonstrate that polyploidy is a universal feature of AURKB inhibitor treatment in all cell types including normal primary cells, but the subsequent outcomes are controlled by RB and p53. We demonstrate that p53 by regulating p21 expression is required for an initial cell cycle arrest by inhibiting both CDK2 and CDK4 activity, but this arrest is only triggered after cells have undergone two failed mitosis and cytokinesis. However, cells can enter senescence in the absence of p53. RB is essential for AURKB inhibitor-induced senescence. AURKB inhibitor induces rapid hypophosphorylation of RB independent of inhibition of CDK2 or CDK4 kinases and p53. This work demonstrates that p53 activation determines the timing of senescence onset, but RB is indispensable for senescence.