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- Title
Inhibition of Aurora B kinase (AURKB) enhances the effectiveness of 5-fluorouracil chemotherapy against colorectal cancer cells.
- Authors
Shah, Esha T.; Molloy, Christopher; Gough, Madeline; Kryza, Thomas; Samuel, Selwin G.; Tucker, Amos; Bhatia, Maneet; Ferguson, Genevieve; Heyman, Rebecca; Vora, Shivam; Monkman, James; Bolderson, Emma; Kulasinghe, Arutha; He, Yaowu; Gabrielli, Brian; Hooper, John D.; Richard, Derek J.; O'Byrne, Kenneth J.; Adams, Mark N.
- Abstract
Background: 5-Fluorouracil (5-FU) remains a core component of systemic therapy for colorectal cancer (CRC). However, response rates remain low, and development of therapy resistance is a primary issue. Combinatorial strategies employing a second agent to augment the therapeutic effect of chemotherapy is predicted to reduce the incidence of treatment resistance and increase the durability of response to therapy. Methods: Here, we employed quantitative proteomics approaches to identify novel druggable proteins and molecular pathways that are deregulated in response to 5-FU, which might serve as targets to improve sensitivity to chemotherapy. Drug combinations were evaluated using 2D and 3D CRC cell line models and an ex vivo culture model of a patient-derived tumour. Results: Quantitative proteomics identified upregulation of the mitosis-associated protein Aurora B (AURKB), within a network of upregulated proteins, in response to a 24 h 5-FU treatment. In CRC cell lines, AURKB inhibition with the dihydrogen phosphate prodrug AZD1152, markedly improved the potency of 5-FU in 2D and 3D in vitro CRC models. Sequential treatment with 5-FU then AZD1152 also enhanced the response of a patient-derived CRC cells to 5-FU in ex vivo cultures. Conclusions: AURKB inhibition may be a rational approach to augment the effectiveness of 5-FU chemotherapy in CRC.
- Publication
British Journal of Cancer, 2024, Vol 130, Issue 7, p1196
- ISSN
0007-0920
- Publication type
Article
- DOI
10.1038/s41416-024-02584-z