Mirna Therapeutics announced today publication of new results in the journal Cancer Research demonstrating proof of concept that the systemic delivery of tumor suppressor microRNAs (miRNA) inhibits tumor growth by restoring the proper regulatory pathways required for cell cycle arrest and apoptosis.
“This recently published data provides proof of concept for our deep pipeline of miRNA-based therapeutic candidates.”
The new study builds on earlier work indicating that suppression of miR-34a contributes to the development of a significant number of solid tumors. A synthetic mimic of miR-34a developed at Mirna formulated with lipid-based nanoparticles was delivered in two different mouse models of non-small cell lung cancer. The systemically delivered miR-34a molecules reduced the expression of multiple miR-34a targets, induced apoptosis, and inhibited growth of established tumors. Intravenous delivery of formulated miR-34a did not cause changes in the serum levels of cytokines or liver and kidney enzymes, suggesting the formulation is well tolerated and does not induce an immune response.
"Tumor suppressor microRNAs provide a new approach to the treatment of cancer. We believe the potent anti-oncogenic activity observed in this study might be explained by the fact that miRNAs target multiple oncogenes and oncogenic pathways. Thus, the ability to affect multiple cancer pathways seems to be a key benefit of therapeutic miRNA mimics. We are pleased with the development progress of miR-34a, one of our lead miRNA therapeutic candidates," said Paul Lammers, M.D., President and CEO. "This recently published data provides proof of concept for our deep pipeline of miRNA-based therapeutic candidates."
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