Updated
Updated · The Straits Times · Aug 23
NUS Finds RX-5902 Cuts Triple-Negative Breast Tumors 90% by Targeting DP103
Updated
Updated · The Straits Times · Aug 23

NUS Finds RX-5902 Cuts Triple-Negative Breast Tumors 90% by Targeting DP103

2 articles · Updated · The Straits Times · Aug 23

Summary

  • RX-5902 shut down DP103, a gene identified as a “master switch” in triple-negative breast cancer, in an NUS Medicine study that points to a new targeted treatment route for the hard-to-treat disease.
  • 21 samples and laboratory models showed the drug cut cancer stem cell viability by 40% to 60%, reduced tumour growth by about 50%, and shrank tumours around 90% while largely sparing healthy cells.
  • 50% of treated laboratory models survived to 70 days or longer, versus none in the untreated group, with researchers saying RX-5902 blocks beta-catenin from entering the nucleus and switches off growth-driving genes.
  • DP103 may also serve as a biomarker to identify patients most likely to benefit, allowing future trials to focus on tumours with high DP103 levels rather than treating all patients the same.
  • Triple-negative breast cancer accounts for about 15% to 20% of breast cancers and lacks common drug targets; NUS said the findings, published in Cell Death and Disease, could also inform therapies for other Wnt-driven cancers.

Insights

Could a single master switch finally cure the most aggressive and untreatable form of breast cancer?
If this experimental drug destroys cancer cells while sparing healthy ones, what delays its mainstream clinical use?
Will blocking cancer at the nuclear level permanently stop tumors from spreading, or will they evolve to survive?