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TransCode Therapeutics study shows survival gains in breast cancer model

A new peer-reviewed study published in the journal Cancers demonstrates that TransCode Therapeutics’ lead candidate, TTX-MC138, significantly extended survival in preclinical models of breast cancer bone metastasis. The research validates the company's approach to inhibiting microRNA-10b, a key driver of cancer progression, using proprietary oligonucleotide nanotechnology.

TransCode Therapeutics study shows survival gains in breast cancer model

The study, led by Dr. Anna Moore of Michigan State University, utilized an image-guided delivery system to concentrate TTX-MC138 in metastatic bone lesions. In the mouse model, the treatment successfully suppressed microRNA-10b expression while simultaneously increasing levels of HOXD10, a protein that functions as a tumor suppressor. Researchers observed no systemic toxicity during the trial, suggesting the therapeutic candidate is well-tolerated even with repeated dosing.

Zdravka Medarova, Chief Scientific Officer at TransCode, noted that these findings underscore the potential of miR-10b inhibition to address metastatic disease, which remains the primary cause of cancer-related mortality. While the company is currently evaluating TTX-MC138 in clinical trials for colorectal cancer, this latest data suggests a broader applicability for the platform across various tumor types where metastasis drives poor patient outcomes.

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