Racura Oncology Limited (ASX:RAC) disclosed on 12 November 2026 that new preclinical data on (E,E)-bisantrene's ability to inhibit MYC gene transcription are being presented as a poster at the Frontiers in Cancer Science (FCS) 2026 Conference in Singapore, with findings identifying (E,E)-bisantrene as the active isomer that stabilises the MYC promoter G-quadruplex structure and reduces MYC gene expression and activity.

Key Points

  • Racura is presenting at the FCS 2026 Conference in Singapore from 11–13 November 2026, with the poster presented on 12 November 2026.
  • Preclinical data confirm (E,E)-bisantrene is the major isomer able to stabilise the MYC promoter G-quadruplex and inhibit MYC gene transcription and reduce MYC protein levels.
  • Light exposure converted (E,E)-bisantrene into less active isomers, resulting in significantly less MYC G-quadruplex stabilisation and inhibition of MYC gene expression and activity.
  • The findings support the use of RC220 in the EMILI, HARNESS and CPACS clinical programs.

Poster Presentation at FCS 2026 Conference

The poster, entitled "Light-Induced Isomerization Attenuates (E,E)-Bisantrene G-Quadruplex Binding and MYC Silencing," was presented at the FCS 2026 Conference held in Singapore from 11 to 13 November 2026. The study was conducted in collaboration with researchers from Racura Oncology and the University of Wollongong. The filing states that these findings build on MYC gene expression inhibition data for (E,E)-bisantrene previously presented at the 2026 American Association for Cancer Research Annual Meeting, and that Racura continues to investigate this mechanism through its ongoing research collaboration with Purdue University.

Preclinical Data on Isomer Activity and Photoisomerization

According to the filing, (E,E)-bisantrene undergoes photoisomerization in solution when exposed to light, generating mixtures of (E,E)-, (E,Z)- and (Z,Z)-bisantrene isomers. CD spectroscopy confirmed that (E,E)-bisantrene stabilises the MYC G-quadruplex, while isomer mixtures containing 62% (E,E)-bisantrene stabilised the G-quadruplex significantly less. Cell viability assays using MDA-MB-231 breast cancer cells showed an IC50 of 266 nM for 100% (E,E)-bisantrene, with decreasing (E,E)-bisantrene content in isomeric mixtures raising the IC50 to between 310 and 825 nM, indicating reduced antiproliferative activity.

Relevance to RC220 Clinical Programs

The filing states that preventing (E,E)-bisantrene photoisomerization is described as critical in clinical studies. The three active clinical programs referenced are CPACS, a Phase 1 study of RC220 with doxorubicin in advanced solid tumours (ClinicalTrials.gov ID: NCT06815575); HARNESS-1, a Phase 1 study of RC220 with osimertinib in EGFR-mutant non-small cell lung cancer (ANZCTR ID: ACTRN12626000325303); and EMILI, a Phase 2b/3 RC220 monotherapy study in relapsed/refractory acute myeloid leukaemia, for which registration is disclosed as pending. The filing attributes the following statement to Racura CEO and MD Dr Daniel Tillett: "Confirming that the (E,E)-isomer is the active form supports our development of RC220 as a proprietary formulation of (E,E)-bisantrene."