Disrupting Disease at the Cellular Source

Traditional brain cancer therapies often fail because they target the rapidly dividing cells of the tumor mass but leave behind a highly resilient subpopulation of cells known as Cancer Stem Cells (CSCs). These cells act as the fundamental source of the tumor, driving inevitable disease recurrence.

RR2 GBM cells treated with CT-179 in cell cycle arrest.
Image credit: Terrence Johns, PhD

GBM cancer cells with OLIG2 (green) in the nucleus of the cells.
Image credit: Human Protein Atlas, www.proteinatlas.org. Image available from v25.proteinatlas.org/ENSG00000205927-OLIG2/subcellular

The Role of OLIG2

In many aggressive CNS malignancies, the survival of CSCs is driven by a master control switch: the OLIG2 transcription factor. OLIG2 not only fuels the unchecked growth of these CSCs but also manipulates the tumor micro-environment, actively suppressing the body's natural immune response and hiding the tumor from attack.

CT-179: A Dual-Action Breakthrough

Action 1

Eradicating Cancer Stem Cells

It directly kills the OLIG2-expressing CSCs, destroying the primary source responsible for tumor recurrence.

Action 2

Reversing Immune Suppression

By silencing OLIG2's influence on the microenvironment, CT-179 reverses tumor-driven immune suppression, turning a "cold" tumor environment "hot" and equipping the body’s innate immune system to fight back.