4.7 Article

Preclinical small molecule WEHI-7326 overcomes drug resistance and elicits response in patient-derived xenograft models of human treatment-refractory tumors

Journal

CELL DEATH & DISEASE
Volume 12, Issue 3, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41419-020-03269-0

Keywords

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Categories

Funding

  1. CRC for Cancer Therapeutics under Australian Government's Cooperative Research Centre scheme, NHMRC from the Australian Government [487922, 1113133]
  2. Viertel Foundation Senior Medical Researcher Fellowship
  3. Stafford Fox Medical Research Foundation
  4. Cancer Council Victoria (Sir Edward Dunlop Fellowship)
  5. Victorian Cancer agency [CRF1020, CRF16014]
  6. Cancer Therapeutics CRC top-up scholarships
  7. Victorian Cancer Agency
  8. Harry Secomb Foundation
  9. Australian Cancer Research Foundation
  10. Victorian Government, Australia
  11. Australian National Health and Medical Research Council (NHMRC)
  12. NHMRC [1057805, 1062702, 1078730, 1037230, APP1119152]
  13. Monash University Technology Research Platform network
  14. Therapeutic Innovation Australia (TIA) through the Australian Government National Collaborative Research Infrastructure Strategy (NCRIS) program
  15. Senior Research Fellowship [1117089]
  16. Australian Post-graduate Awards
  17. National Health and Medical Research Council of Australia [1078730, 1062702, 1057805] Funding Source: NHMRC

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Targeting cell division by the new small molecule WEHI-7326 shows promising anti-tumor activity with broad-spectrum efficacy, providing a potential new therapeutic option for cancer patients.
Targeting cell division by chemotherapy is a highly effective strategy to treat a wide range of cancers. However, there are limitations of many standard-of-care chemotherapies: undesirable drug toxicity, side-effects, resistance and high cost. New small molecules which kill a wide range of cancer subtypes, with good therapeutic window in vivo, have the potential to complement the current arsenal of anti-cancer agents and deliver improved safety profiles for cancer patients. We describe results with a new anti-cancer small molecule, WEHI-7326, which causes cell cycle arrest in G2/M, cell death in vitro, and displays efficacious anti-tumor activity in vivo. WEHI-7326 induces cell death in a broad range of cancer cell lines, including taxane-resistant cells, and inhibits growth of human colon, brain, lung, prostate and breast tumors in mice xenografts. Importantly, the compound elicits tumor responses as a single agent in patient-derived xenografts of clinically aggressive, treatment-refractory neuroblastoma, breast, lung and ovarian cancer. In combination with standard-of-care, WEHI-7326 induces a remarkable complete response in a mouse model of high-risk neuroblastoma. WEHI-7326 is mechanistically distinct from known microtubule-targeting agents and blocks cells early in mitosis to inhibit cell division, ultimately leading to apoptotic cell death. The compound is simple to produce and possesses favorable pharmacokinetic and toxicity profiles in rodents. It represents a novel class of anti-cancer therapeutics with excellent potential for further development due to the ease of synthesis, simple formulation, moderate side effects and potent in vivo activity. WEHI-7326 has the potential to complement current frontline anti-cancer drugs and to overcome drug resistance in a wide range of cancers.

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